The document provides an analysis of therapy provision for carers at the Centre for Health and Well Being. It includes a literature review on complementary therapies, mental health, and carers in the UK. An anonymous survey of 85 carers who received services through the centre was conducted. Key findings include: 47% of carers cared for older people, emotional support and household tasks were most common help provided, 55% of carers provided over 100 hours of care, 95% of challenges were emotional, 65% received no formal support, and 89% suffered from stress and worry. The majority found the complementary therapies brought stress relief and rated the services as excellent. Recommendations include the need for increased support for carers.
We’re always ready to take on board the views of the people who matter most: it’s what helps us focus on providing products and services that people really need. This is the tenth year in which we’ve conducted our Health of the Nation study, canvassing the opinions of GPs right across the UK. This year we’ve extended our research to include the views of 1,000 patients to understand their experiences of healthcare in the UK.
Ireta- Institute for Research, Education and Training in Addictions- FY 2018Cassondra Turner McArthur
Concrete Ways to Shift from Punitive to
Therapeutic Responses to Addiction......
...........IRETA’s Projects ..........................................................................7
Clinical Quality Improvement..............................................7
Technical Assistance...........................................................7
Training and Education .......................................................8
Applied Research ..............................................................10
Community Events.
ACUPUNCTURE SCIENCE ASSOCIATION Conference 2015 Ludhiana Punjab
Title
NADA Protocol for addiction treatment in India- In retrospect
Authors
Suneel Vatsyayan*, Dr. Ajay Vats**,
Abstract
In the mid-1970s, Michael Smith, a medical doctor at Lincoln Hospital in the South Bronx area of New York, modified an existing system of auricular acupuncture into a simple technique for the treatment of many common drug addictions as an alternative to methadone. This selection of three to five ear points proved to be extremely effective in the treatment of addictions, and became what is now referred to as the “NADA protocol.”
Dozens of studies have documented the effectiveness of the NADA protocol as an adjunct treatment. Among the benefits reported by patients and health care providers are: improved retention in drug treatment programs; more optimistic attitudes about detoxification and recovery; reductions in cravings and anxiety; fewer episodes of sleep disturbance; and reduced need for pharmaceuticals.
While the NADA protocol is an important component of any detoxification program, it is by no means the only component. The NADA protocol is often used with other treatment modalities, such as counseling, support groups and self-help programs, to increase the overall effectiveness of care.
In 1999, NADA protocol was introduced in India under the supervision of Dr. Michael O. Smith with the objective of making barrier free services and well-being issues available across communities. The proposed paper is a journey in retrospect of NADA protocol globally and India in particular. The paper focuses on issues related to addiction treatment, NADA Protocol, its spread globally and how NADA protocol can meet the needs and challenges in the field of addiction treatment & rehabilitation in India.
Contact Information
Mob.9810594544,
nadaindia@gmail.com
acudetoxindia@gmail.com
*Chairman, Nada India Foundation
(www.nadaindia.info)
**Chairman, Indian Association of
Acupuncture Detoxification Specialist (IAADS)
(www.acudetoxindia.com )
This document discusses the statutory duty of candour that was introduced in the UK via the Care Act 2014 and Health and Social Care Act 2008. It requires healthcare providers to be open and honest with patients when certain "notifiable safety incidents" have occurred that resulted in harm. It defines what constitutes a notifiable incident and outlines the requirements for notifying patients of incidents and providing follow up information. It discusses how this interacts with claims processes and considers some case studies to demonstrate how the duty of candour would apply in different clinical situations. The goal of the duty of candour is to improve openness and transparency when things go wrong in healthcare.
The document discusses mental health challenges and initiatives in India. It outlines 7 key challenges: 1) large unmet need for care, 2) lack of understanding that psychological issues require treatment, 3) limited acceptance of modern care, 4) insufficient mental health services and professionals, 5) underutilization of existing services, 6) difficulties with recovery and reintegration, 7) lack of organized systems. It then details various national initiatives over decades to address these, including developing community-based care and integrating mental health into general health services.
This document provides an overview of the adult mental health pathway and services offered by Northamptonshire Healthcare NHS Foundation Trust. It describes several services including the Mental Health Wellbeing Navigation Team, Improving Access to Psychological Therapies (IAPT), Primary Care Liaison Workers, memory assessment services, Planned Care and Recovery Teams, Urgent Care and Assessment Teams, Crisis and Telephone Support Service, inpatient services, and more. For each service, it provides brief details on what they do, who they can help, where care can be received, typical treatment length and next steps. The overall document aims to help people understand the options available to them and how to navigate the mental health system in Northamptonshire.
The document provides guidance for stroke patients recovering at home. It emphasizes the importance of following doctors' advice, adapting one's home for needs, maintaining follow-up bloodwork and therapy schedules, and establishing a routine. It recommends speaking to discharge planners early to determine the best recovery option, assessing support needs, and setting achievable goals to smoothly transition from hospital to home.
Home-Based Crisis Team (Dr Sinead O'Brien - part 1 of 3)Keren Lilley
The document summarizes the Home Based Crisis Team serving the City North sector of Cork, Ireland. It describes the team's mission to provide home-based crisis assessment and treatment for individuals with acute psychiatric illness. It notes that the majority of admissions to the local acute unit previously came from City North sectors. The document also provides context about the socioeconomic challenges faced in City North communities and the doctor's vision for the future of the Home Based Crisis Team, which includes evidence-based practice, intensive case management, research, and a focus on patients' overall health and well-being.
We’re always ready to take on board the views of the people who matter most: it’s what helps us focus on providing products and services that people really need. This is the tenth year in which we’ve conducted our Health of the Nation study, canvassing the opinions of GPs right across the UK. This year we’ve extended our research to include the views of 1,000 patients to understand their experiences of healthcare in the UK.
Ireta- Institute for Research, Education and Training in Addictions- FY 2018Cassondra Turner McArthur
Concrete Ways to Shift from Punitive to
Therapeutic Responses to Addiction......
...........IRETA’s Projects ..........................................................................7
Clinical Quality Improvement..............................................7
Technical Assistance...........................................................7
Training and Education .......................................................8
Applied Research ..............................................................10
Community Events.
ACUPUNCTURE SCIENCE ASSOCIATION Conference 2015 Ludhiana Punjab
Title
NADA Protocol for addiction treatment in India- In retrospect
Authors
Suneel Vatsyayan*, Dr. Ajay Vats**,
Abstract
In the mid-1970s, Michael Smith, a medical doctor at Lincoln Hospital in the South Bronx area of New York, modified an existing system of auricular acupuncture into a simple technique for the treatment of many common drug addictions as an alternative to methadone. This selection of three to five ear points proved to be extremely effective in the treatment of addictions, and became what is now referred to as the “NADA protocol.”
Dozens of studies have documented the effectiveness of the NADA protocol as an adjunct treatment. Among the benefits reported by patients and health care providers are: improved retention in drug treatment programs; more optimistic attitudes about detoxification and recovery; reductions in cravings and anxiety; fewer episodes of sleep disturbance; and reduced need for pharmaceuticals.
While the NADA protocol is an important component of any detoxification program, it is by no means the only component. The NADA protocol is often used with other treatment modalities, such as counseling, support groups and self-help programs, to increase the overall effectiveness of care.
In 1999, NADA protocol was introduced in India under the supervision of Dr. Michael O. Smith with the objective of making barrier free services and well-being issues available across communities. The proposed paper is a journey in retrospect of NADA protocol globally and India in particular. The paper focuses on issues related to addiction treatment, NADA Protocol, its spread globally and how NADA protocol can meet the needs and challenges in the field of addiction treatment & rehabilitation in India.
Contact Information
Mob.9810594544,
nadaindia@gmail.com
acudetoxindia@gmail.com
*Chairman, Nada India Foundation
(www.nadaindia.info)
**Chairman, Indian Association of
Acupuncture Detoxification Specialist (IAADS)
(www.acudetoxindia.com )
This document discusses the statutory duty of candour that was introduced in the UK via the Care Act 2014 and Health and Social Care Act 2008. It requires healthcare providers to be open and honest with patients when certain "notifiable safety incidents" have occurred that resulted in harm. It defines what constitutes a notifiable incident and outlines the requirements for notifying patients of incidents and providing follow up information. It discusses how this interacts with claims processes and considers some case studies to demonstrate how the duty of candour would apply in different clinical situations. The goal of the duty of candour is to improve openness and transparency when things go wrong in healthcare.
The document discusses mental health challenges and initiatives in India. It outlines 7 key challenges: 1) large unmet need for care, 2) lack of understanding that psychological issues require treatment, 3) limited acceptance of modern care, 4) insufficient mental health services and professionals, 5) underutilization of existing services, 6) difficulties with recovery and reintegration, 7) lack of organized systems. It then details various national initiatives over decades to address these, including developing community-based care and integrating mental health into general health services.
This document provides an overview of the adult mental health pathway and services offered by Northamptonshire Healthcare NHS Foundation Trust. It describes several services including the Mental Health Wellbeing Navigation Team, Improving Access to Psychological Therapies (IAPT), Primary Care Liaison Workers, memory assessment services, Planned Care and Recovery Teams, Urgent Care and Assessment Teams, Crisis and Telephone Support Service, inpatient services, and more. For each service, it provides brief details on what they do, who they can help, where care can be received, typical treatment length and next steps. The overall document aims to help people understand the options available to them and how to navigate the mental health system in Northamptonshire.
The document provides guidance for stroke patients recovering at home. It emphasizes the importance of following doctors' advice, adapting one's home for needs, maintaining follow-up bloodwork and therapy schedules, and establishing a routine. It recommends speaking to discharge planners early to determine the best recovery option, assessing support needs, and setting achievable goals to smoothly transition from hospital to home.
Home-Based Crisis Team (Dr Sinead O'Brien - part 1 of 3)Keren Lilley
The document summarizes the Home Based Crisis Team serving the City North sector of Cork, Ireland. It describes the team's mission to provide home-based crisis assessment and treatment for individuals with acute psychiatric illness. It notes that the majority of admissions to the local acute unit previously came from City North sectors. The document also provides context about the socioeconomic challenges faced in City North communities and the doctor's vision for the future of the Home Based Crisis Team, which includes evidence-based practice, intensive case management, research, and a focus on patients' overall health and well-being.
Pt 3 - Home-based Crisis Team (Dr Sinead O'Brien)Keren Lilley
Dr Sinead O'Brien's talk on "Home Based Crisis Team: initial steps towards recovery in the community" at the conference "Home Based Recovery and Wellness in Mental Health" - jointly hosted by University College Cork and the Centre for Recovery and Social Inclusion, Cork on the 9th June 2010. Final part of 3 segments
Evidence shows us that specialised mood disorder clinics deliver cost savings, better clinical outcomes and improved patient satisfaction. Presented to the Trent Division of the Royal College of Psychiatrists, November 2013, Sheffield.
PhD Thesis Louise Byrne LivedExperinceMHrolesLouise Byrne
This doctoral thesis explores the lived experiences of mental health practitioners with lived experience of mental illness. Semi-structured interviews and focus groups were conducted with lived experience practitioners across several Australian states. A grounded theory approach was used to analyze the data and develop a substantive theory. The theory that emerged is that stigma, both overt and covert, underlies the experiences of lived experience practitioners and impacts their roles. As a result, lived experience practitioners knowingly risk their own well-being and recovery to benefit current mental health consumers. When workplaces are more supportive and less stigmatizing, there is less risk to lived experience practitioners and greater benefits for consumers. For these roles to reach their full potential and benefit both consumers and practitioners, the
Leadership at the Bedside – Making the Change that Needs to HappenBCCPA
The document discusses leadership at the bedside and the need for change in nursing care delivery models. It notes that current models emphasize teamwork and collaboration more than previous models. The presentation defines key terms related to nursing care delivery and leadership. It discusses progressive patient care models and the roles of licensed practical nurses and health care assistants in leading teams. It argues that LPNs and HCAs are well-educated and able to provide critical thinking and leadership at the bedside.
Dr Scott Payne & Dr Mark Owens: ARBD in the Northern Irish Context AlcoholForum.org
The document summarizes research conducted on alcohol-related brain damage (ARBD) in the Western Health and Social Care Trust area of Northern Ireland. It established a prevalence rate of 9 per 10,000 people and identified 278 individuals with ARBD through data collection from health and social care agencies. Care pathways were informed by the research findings to help improve services for individuals with ARBD.
This document summarizes key points from an article about improving spiritual care in hospice settings. It discusses how spiritual care professionals can contribute to quality of care through areas like managing pain, family conflicts, and falls prevention. It also emphasizes the importance of reasonable caseloads and support for spiritual care teams. The document recommends that hospices evaluate their spiritual care services and credentials of chaplains using guidelines and certifications from organizations like the Association for Professional Chaplains. Hospices are encouraged to help spiritual care providers advance their skills and certifications over time.
BeHealth.Today | Mobile Psych Treatment TeamKevin Popović
The Mobile Psychiatric Treatment Team (MPTT) provides an alternative to emergency room boarding and inpatient psychiatric hospitalization. The MPTT consists of a multidisciplinary team including a psychiatrist, psychiatric nurse, licensed clinical social worker, mental health worker, and peer support specialist. They provide immediate mental health treatment, evaluation, medication management, therapy and safety planning to stabilize patients within 24 hours, allowing discharge from the emergency room to an appropriate level of care. The MPTT aims to address the problems of lack of treatment for patients boarding in emergency rooms while awaiting inpatient beds by bringing specialized mental health care directly to the patient.
Pt 2 - Home-Based Crisis Team (Dr Sinead O'Brien - part 2 of 3)Keren Lilley
Dr Sinead O'Brien's talk on "Home Based Crisis Team: initial steps towards recovery in the community" at the conference "Home Based Recovery and Wellness in Mental Health" - jointly hosted by University College Cork and the Centre for Recovery and Social Inclusion, Cork on the 9th June 2010. Part 2 of 3 segments
Mr Grant Brand: Lessons Learned in the First Nine Years of the Glasgow ARBD TeamAlcoholForum.org
The document summarizes lessons learned from the first nine years of the Glasgow Alcohol Related Brain Damage (ARBD) Team. It discusses how the team was set up, missed opportunities at the beginning, and what they have learned over time. Key points include broadening the referral criteria, conducting thorough multidisciplinary assessments, using legislation to help with harm reduction, providing rehabilitation services, and training other services on ARBD. It emphasizes the need for a public health approach, clear strategy, and person-centered flexible services for those with ARBD.
The document discusses community psychiatry and hospital-based community psychiatry services. It describes the components of hospital-based services including assertive community teams and acute home care. It provides criteria for inclusion in these programs and the functions of the teams which include assessment, home visits, interventions, and rehabilitation. The document also describes community mental health centers and their role in providing accessible, continuing treatment for mental disorders in the community.
Person Centered Care through Integrating a Palliative Approach: Lessons from ...BCCPA
Aging adults are entering residential care facilities with more advanced disease than in the past and their length of stay is shorter. Most health care providers in these facilities do not receive targeted education and training in palliative care, nor are they confident to have crucial conversations about goals of care and end of life challenges with residents and their families. Due to limited capacity to manage predictable symptoms related to end of life and insufficient planning, many residents are transferred to hospital in crisis and die in the Emergency Department or acute care wards.
This presentation will showcase some of the initiatives by identifying common themes, unique features of each and strategies for success. Opportunity will be given for delegates to ask questions and brainstorm how lessons learned from these initiatives could inform the care provided at their own facility.
Presented by:
- Jane Webley, RN LLB Regional lead, End of Life, Vancouver Coastal Health (EPAIRS and the Daisy project)
- Dr Christine Jones, Island Health (SSC project: Improving end of life outcomes in residential care facilities: A palliative approach to care)
- Kathleen Yue, RN, BSN, MN, CHPCN (c) Education Coordinator, BC Center for Palliative Care
This document discusses self-care for patients with long-term conditions. It notes that over 15 million people in England live with at least one long-term condition, accounting for most NHS spending. Self-care is defined as individuals taking responsibility for their own health and well-being with support from healthcare professionals. This includes maintaining health, meeting needs, preventing illness, and managing conditions. Supported self-care can improve health outcomes, patient satisfaction, and empower patients to take more control.
DR CHRISTOS KOUIMTSIDIS - ALCOHOL MISUSE IN SPECIAL POPULATIONS: INTELLECTUAL...iCAADEvents
There is little and con icting evidence on the prevalence of alcohol misuse and treatment available for people with Intellectual Disabilities (also referred as Learning Disabilities). As is similar to other vulnerable populations, adults with ID have increasingly lived more independently in the community following the closure of long-stay hospitals. This has increased their exposure to environmental stressors and substance and alcohol misuse, negatively impacting on their functioning, relationships, physical and mental health, and safety. Traumatic Brain Injury (TBI) is the most common cause of disability in younger adults. Yet the community care for patients with TBI varies hugely in the UK. There is a well-established link between TBI and alcohol misuse, with both TBI leading to increased levels of alcohol misuse and alcohol misuse contributing to risk of TBIs. The effects of neuronal damage have been shown to increase after TBI accompanied by alcohol intoxication.This presentation is based on the experience gained from the rst in the UK feasibility study on this topic, and draws from the experience of setting up and running the first ever pilot of a combined TBI and alcohol brief intervention service in London.
Is Home Really Best? Private Home Care Agencies and Technology Can Make Home ...BCCPA
This presentation is about how technology can increase family involvement in person-centred care planning in home care. The Conference will be the first time the results from this UBC Masters Research project will be presented.
In a 2017 UBC survey of home care agencies in greater Vancouver the study aimed to determine
1) what are these home care agencies challenges in providing quality person centred care to their clients
2) home care agencies perceived benefits and barriers in using health information technologies.
Survey findings will help both public and private care providers understand how to better collaborate in caring for aging seniors.
Presented by: Christina Chiu, CEO, CareCrew, MHA Candidate
The My Mind Lab assessment provides a multi-dimensional behavioral health screening for depression, bipolar disorder, anxiety, PTSD, and substance use in a quick and easy to administer test. The assessment increases quality of patient care, enhances a practice's image, and incorporates digitized health records while helping to increase revenue. It can be used by medical practices, hospitals, managed care organizations, and other providers to better identify and treat underlying mental health issues, track patient progress, and submit claims under CPT code 96103 for reimbursement. The assessment takes on average less than 10 minutes for patients to complete and provides immediate scoring and reporting to help physicians.
PEGS, palliation and planning: Issues in caring for people with advanced MSMS Trust
This document discusses issues related to palliative care and advance care planning for people with advanced multiple sclerosis. It provides an overview of palliative care approaches, the legal and ethical basis for palliation and planning, and specific palliative issues in MS. It also covers topics like advance decisions to refuse treatment, common issues with writing advance refusal documents, and what to do when faced with an advance care plan. The objectives are to understand challenges with advance care planning and outline specific issues regarding planning in MS.
Evidence-Informed Guidelines for Recreation Therapy programs to Enhance the M...BCCPA
This presentation will provide an overview of the BCCPA Mitacs-SFU project to develop a best practices guide for recreational therapy (RT). OLTCA and ACCA are also partners in this project. Along with reviewing the results of a survey on recreational therapy in LTC that was undertaken in BC, Alberta and Ontario it will present the final RT best practices guide.
Presented by:
- Dr. Kim van Schooten, Centre for Hip Health and Mobility, University of British Columbia
- Dr. Yijian Yang, Centre for Hip Health and Mobility, University of British Columbia
- Brenda Kinch, President, BC Therapeutic Recreation Association
This study assessed the spiritual health of 990 elderly people in Jaipur, India. It found that the majority (68.89%) had poor spiritual health according to the Spiritual Health Assessment Scale. Poorer spiritual health was strongly associated with poorer psycho-wellness. The study also found that self-realization, the deepest domain of spirituality, had the lowest mean score, followed by self-actualization and then self-development. In conclusion, poorer spiritual health among the elderly leads to poorer psycho-wellness.
Presentations from the Commitment for Carers meeting held in London on 5 December 2013
#NHSThinkCarer
organised by NHS Improving Quality and NHS England
The document describes efforts to improve psychosis care through the Treatment and Recovery In PsycHosis (TRIumPH) program. The key points are:
1) A working group was established between Southern Health NHS Foundation Trust and Wessex Academic Health Science Network to improve assessment and treatment for people experiencing psychosis based on understanding gaps in existing care.
2) The program developed and implemented a standardized care pathway across four Early Intervention in Psychosis teams, improving access to assessment and treatment.
3) Feedback from service users, carers, and clinicians informed the work, which aimed to provide more compassionate, holistic, and recovery-focused care.
This webinar will have two perspectives.
Jasveen will be presenting about the impact of cancer and treatment on a person’s physical, cognitive & mental health and how an Occupational therapist can work with the person to gradually overcome these challenges to return to work with or without modifications. The presentation will cover some case studies of past success with the opportunity to answer questions at the end.
Then we will hear from Jen who has experienced her own journey with breast cancer and how she advocated for herself and occupational therapy to help her return to full time employment.
- Coaching with Substance provides recovery coaching and training to help clients overcome addiction issues. In the past year they served 131 clients through coaching and trained 4 students. They engaged 29 volunteers and held 12 community events.
- Their annual report outlines their services, achievements for the year including awards and media coverage, and financial details. They generated over $90,000 in revenue and spent $78,000 on expenses. With a donation of $42,000 from the founder, they had a net profit of over $12,000.
- The founder and spiritual trainer contributed many pro bono hours. Financially, this was the charity's most successful year compared to prior years.
Pt 3 - Home-based Crisis Team (Dr Sinead O'Brien)Keren Lilley
Dr Sinead O'Brien's talk on "Home Based Crisis Team: initial steps towards recovery in the community" at the conference "Home Based Recovery and Wellness in Mental Health" - jointly hosted by University College Cork and the Centre for Recovery and Social Inclusion, Cork on the 9th June 2010. Final part of 3 segments
Evidence shows us that specialised mood disorder clinics deliver cost savings, better clinical outcomes and improved patient satisfaction. Presented to the Trent Division of the Royal College of Psychiatrists, November 2013, Sheffield.
PhD Thesis Louise Byrne LivedExperinceMHrolesLouise Byrne
This doctoral thesis explores the lived experiences of mental health practitioners with lived experience of mental illness. Semi-structured interviews and focus groups were conducted with lived experience practitioners across several Australian states. A grounded theory approach was used to analyze the data and develop a substantive theory. The theory that emerged is that stigma, both overt and covert, underlies the experiences of lived experience practitioners and impacts their roles. As a result, lived experience practitioners knowingly risk their own well-being and recovery to benefit current mental health consumers. When workplaces are more supportive and less stigmatizing, there is less risk to lived experience practitioners and greater benefits for consumers. For these roles to reach their full potential and benefit both consumers and practitioners, the
Leadership at the Bedside – Making the Change that Needs to HappenBCCPA
The document discusses leadership at the bedside and the need for change in nursing care delivery models. It notes that current models emphasize teamwork and collaboration more than previous models. The presentation defines key terms related to nursing care delivery and leadership. It discusses progressive patient care models and the roles of licensed practical nurses and health care assistants in leading teams. It argues that LPNs and HCAs are well-educated and able to provide critical thinking and leadership at the bedside.
Dr Scott Payne & Dr Mark Owens: ARBD in the Northern Irish Context AlcoholForum.org
The document summarizes research conducted on alcohol-related brain damage (ARBD) in the Western Health and Social Care Trust area of Northern Ireland. It established a prevalence rate of 9 per 10,000 people and identified 278 individuals with ARBD through data collection from health and social care agencies. Care pathways were informed by the research findings to help improve services for individuals with ARBD.
This document summarizes key points from an article about improving spiritual care in hospice settings. It discusses how spiritual care professionals can contribute to quality of care through areas like managing pain, family conflicts, and falls prevention. It also emphasizes the importance of reasonable caseloads and support for spiritual care teams. The document recommends that hospices evaluate their spiritual care services and credentials of chaplains using guidelines and certifications from organizations like the Association for Professional Chaplains. Hospices are encouraged to help spiritual care providers advance their skills and certifications over time.
BeHealth.Today | Mobile Psych Treatment TeamKevin Popović
The Mobile Psychiatric Treatment Team (MPTT) provides an alternative to emergency room boarding and inpatient psychiatric hospitalization. The MPTT consists of a multidisciplinary team including a psychiatrist, psychiatric nurse, licensed clinical social worker, mental health worker, and peer support specialist. They provide immediate mental health treatment, evaluation, medication management, therapy and safety planning to stabilize patients within 24 hours, allowing discharge from the emergency room to an appropriate level of care. The MPTT aims to address the problems of lack of treatment for patients boarding in emergency rooms while awaiting inpatient beds by bringing specialized mental health care directly to the patient.
Pt 2 - Home-Based Crisis Team (Dr Sinead O'Brien - part 2 of 3)Keren Lilley
Dr Sinead O'Brien's talk on "Home Based Crisis Team: initial steps towards recovery in the community" at the conference "Home Based Recovery and Wellness in Mental Health" - jointly hosted by University College Cork and the Centre for Recovery and Social Inclusion, Cork on the 9th June 2010. Part 2 of 3 segments
Mr Grant Brand: Lessons Learned in the First Nine Years of the Glasgow ARBD TeamAlcoholForum.org
The document summarizes lessons learned from the first nine years of the Glasgow Alcohol Related Brain Damage (ARBD) Team. It discusses how the team was set up, missed opportunities at the beginning, and what they have learned over time. Key points include broadening the referral criteria, conducting thorough multidisciplinary assessments, using legislation to help with harm reduction, providing rehabilitation services, and training other services on ARBD. It emphasizes the need for a public health approach, clear strategy, and person-centered flexible services for those with ARBD.
The document discusses community psychiatry and hospital-based community psychiatry services. It describes the components of hospital-based services including assertive community teams and acute home care. It provides criteria for inclusion in these programs and the functions of the teams which include assessment, home visits, interventions, and rehabilitation. The document also describes community mental health centers and their role in providing accessible, continuing treatment for mental disorders in the community.
Person Centered Care through Integrating a Palliative Approach: Lessons from ...BCCPA
Aging adults are entering residential care facilities with more advanced disease than in the past and their length of stay is shorter. Most health care providers in these facilities do not receive targeted education and training in palliative care, nor are they confident to have crucial conversations about goals of care and end of life challenges with residents and their families. Due to limited capacity to manage predictable symptoms related to end of life and insufficient planning, many residents are transferred to hospital in crisis and die in the Emergency Department or acute care wards.
This presentation will showcase some of the initiatives by identifying common themes, unique features of each and strategies for success. Opportunity will be given for delegates to ask questions and brainstorm how lessons learned from these initiatives could inform the care provided at their own facility.
Presented by:
- Jane Webley, RN LLB Regional lead, End of Life, Vancouver Coastal Health (EPAIRS and the Daisy project)
- Dr Christine Jones, Island Health (SSC project: Improving end of life outcomes in residential care facilities: A palliative approach to care)
- Kathleen Yue, RN, BSN, MN, CHPCN (c) Education Coordinator, BC Center for Palliative Care
This document discusses self-care for patients with long-term conditions. It notes that over 15 million people in England live with at least one long-term condition, accounting for most NHS spending. Self-care is defined as individuals taking responsibility for their own health and well-being with support from healthcare professionals. This includes maintaining health, meeting needs, preventing illness, and managing conditions. Supported self-care can improve health outcomes, patient satisfaction, and empower patients to take more control.
DR CHRISTOS KOUIMTSIDIS - ALCOHOL MISUSE IN SPECIAL POPULATIONS: INTELLECTUAL...iCAADEvents
There is little and con icting evidence on the prevalence of alcohol misuse and treatment available for people with Intellectual Disabilities (also referred as Learning Disabilities). As is similar to other vulnerable populations, adults with ID have increasingly lived more independently in the community following the closure of long-stay hospitals. This has increased their exposure to environmental stressors and substance and alcohol misuse, negatively impacting on their functioning, relationships, physical and mental health, and safety. Traumatic Brain Injury (TBI) is the most common cause of disability in younger adults. Yet the community care for patients with TBI varies hugely in the UK. There is a well-established link between TBI and alcohol misuse, with both TBI leading to increased levels of alcohol misuse and alcohol misuse contributing to risk of TBIs. The effects of neuronal damage have been shown to increase after TBI accompanied by alcohol intoxication.This presentation is based on the experience gained from the rst in the UK feasibility study on this topic, and draws from the experience of setting up and running the first ever pilot of a combined TBI and alcohol brief intervention service in London.
Is Home Really Best? Private Home Care Agencies and Technology Can Make Home ...BCCPA
This presentation is about how technology can increase family involvement in person-centred care planning in home care. The Conference will be the first time the results from this UBC Masters Research project will be presented.
In a 2017 UBC survey of home care agencies in greater Vancouver the study aimed to determine
1) what are these home care agencies challenges in providing quality person centred care to their clients
2) home care agencies perceived benefits and barriers in using health information technologies.
Survey findings will help both public and private care providers understand how to better collaborate in caring for aging seniors.
Presented by: Christina Chiu, CEO, CareCrew, MHA Candidate
The My Mind Lab assessment provides a multi-dimensional behavioral health screening for depression, bipolar disorder, anxiety, PTSD, and substance use in a quick and easy to administer test. The assessment increases quality of patient care, enhances a practice's image, and incorporates digitized health records while helping to increase revenue. It can be used by medical practices, hospitals, managed care organizations, and other providers to better identify and treat underlying mental health issues, track patient progress, and submit claims under CPT code 96103 for reimbursement. The assessment takes on average less than 10 minutes for patients to complete and provides immediate scoring and reporting to help physicians.
PEGS, palliation and planning: Issues in caring for people with advanced MSMS Trust
This document discusses issues related to palliative care and advance care planning for people with advanced multiple sclerosis. It provides an overview of palliative care approaches, the legal and ethical basis for palliation and planning, and specific palliative issues in MS. It also covers topics like advance decisions to refuse treatment, common issues with writing advance refusal documents, and what to do when faced with an advance care plan. The objectives are to understand challenges with advance care planning and outline specific issues regarding planning in MS.
Evidence-Informed Guidelines for Recreation Therapy programs to Enhance the M...BCCPA
This presentation will provide an overview of the BCCPA Mitacs-SFU project to develop a best practices guide for recreational therapy (RT). OLTCA and ACCA are also partners in this project. Along with reviewing the results of a survey on recreational therapy in LTC that was undertaken in BC, Alberta and Ontario it will present the final RT best practices guide.
Presented by:
- Dr. Kim van Schooten, Centre for Hip Health and Mobility, University of British Columbia
- Dr. Yijian Yang, Centre for Hip Health and Mobility, University of British Columbia
- Brenda Kinch, President, BC Therapeutic Recreation Association
This study assessed the spiritual health of 990 elderly people in Jaipur, India. It found that the majority (68.89%) had poor spiritual health according to the Spiritual Health Assessment Scale. Poorer spiritual health was strongly associated with poorer psycho-wellness. The study also found that self-realization, the deepest domain of spirituality, had the lowest mean score, followed by self-actualization and then self-development. In conclusion, poorer spiritual health among the elderly leads to poorer psycho-wellness.
Presentations from the Commitment for Carers meeting held in London on 5 December 2013
#NHSThinkCarer
organised by NHS Improving Quality and NHS England
The document describes efforts to improve psychosis care through the Treatment and Recovery In PsycHosis (TRIumPH) program. The key points are:
1) A working group was established between Southern Health NHS Foundation Trust and Wessex Academic Health Science Network to improve assessment and treatment for people experiencing psychosis based on understanding gaps in existing care.
2) The program developed and implemented a standardized care pathway across four Early Intervention in Psychosis teams, improving access to assessment and treatment.
3) Feedback from service users, carers, and clinicians informed the work, which aimed to provide more compassionate, holistic, and recovery-focused care.
This webinar will have two perspectives.
Jasveen will be presenting about the impact of cancer and treatment on a person’s physical, cognitive & mental health and how an Occupational therapist can work with the person to gradually overcome these challenges to return to work with or without modifications. The presentation will cover some case studies of past success with the opportunity to answer questions at the end.
Then we will hear from Jen who has experienced her own journey with breast cancer and how she advocated for herself and occupational therapy to help her return to full time employment.
- Coaching with Substance provides recovery coaching and training to help clients overcome addiction issues. In the past year they served 131 clients through coaching and trained 4 students. They engaged 29 volunteers and held 12 community events.
- Their annual report outlines their services, achievements for the year including awards and media coverage, and financial details. They generated over $90,000 in revenue and spent $78,000 on expenses. With a donation of $42,000 from the founder, they had a net profit of over $12,000.
- The founder and spiritual trainer contributed many pro bono hours. Financially, this was the charity's most successful year compared to prior years.
QUALITY IMPROVEMENT PROJECT: PROVISION OF GRIEF COUNSELLING TO MOTHERS WHO HA...Achoka Clifford
QUALITY IMPROVEMENT PROJECT: PROVISION OF GRIEF COUNSELLING TO MOTHERS WHO HAVE LOST THEIR BABIES.
It is a study under leadership and management course in nursing school.
It provides enough details on quality improvement projects that can be done on hospital especially to postnatal mothers who has lost their children.
It is a project that was done to reduce effects of bereavement on mothers that might lead to mental damage hence impact on quality of care in generally
The document discusses the need for more patient-centered chronic care that takes a holistic approach and moves care closer to home. It provides examples of how optimizing care pathways for patients with conditions like diabetes or who experience falls can lead to better outcomes and lower costs. Reducing unwarranted variations in care across regions and implementing evidence-based approaches like NHS RightCare that involve clinicians can help standardize best practices and deliver value. However, fully coordinated care requires alignment between health and social care partners.
Hello Sir
We are a premier academic writing agency with industry partners in UK, Australia and Middle East and over 15 years of experience. We are looking to establish long-term relationships with industry partners and would love to discuss this opportunity further with you.
Thanks & Regards
visit our website.
www.onlineassignmenthelp.com.au
www.freeassignmenthelp.com
www.btechndassignment.cheapassignmenthelp.co.uk
www.cheapassignmenthelp.com
www.cheapassignmenthelp.co.uk/
Emergency Psychiatry clinical and training approaches.pdfFazelFadhilah
This document discusses emergency psychiatry training in Canada based on a survey of psychiatry residency programs. It finds there is significant variability across programs in the structure and duration of emergency psychiatry clinical exposure and teaching. Most programs provide 1-5 weeks of clinical training in a variety of settings, including designated psychiatric emergency units in general hospitals. Teaching methods and duration also vary widely. The document advocates for improved standardization of clinical training and didactic teaching to better address the needs of the emergency psychiatric population. It also discusses different systems and settings for emergency psychiatry assessments, noting the advantages and safety features of general hospital and psychiatric hospital models.
This document discusses best practice primary health care for clients with chronic diseases. It describes the 2017 NACCHO Members Conference theme of "Our Health Counts: Yesterday, Today and Tomorrow". The document outlines Gurriny's model of care, which includes an Integrated Team Care program and engagement in health promotion. It also presents a case study of a client named Aunty J who accessed various chronic disease services including dietitians, diabetes educators, and medication reviews through the coordinated care provided by Gurriny.
The document discusses mental health services in the UK for depression. It provides statistics on depression prevalence and details primary and secondary care systems for mental health. Primary care focuses on diagnosis, management and prevention, while secondary care handles more severe cases, like those involving psychosis or hospitalization. The document critiques gaps in primary care for mental health and outlines guidelines and pathways to improve treatment, such as increasing accessibility and using evidence-based therapies like CBT.
The document discusses the evolution of mental health services from the 20th to 21st century. It describes how quality of care, community-based services, and clinical governance were prioritized in restructuring an Irish mental health service based on a mission of independent, human rights-based and recovery-focused care. Key metrics like length of stay, readmission rates, and user satisfaction improved under this new model.
The document discusses palliative care, what it is, and its benefits. It provides evidence that palliative care can improve quality of life for patients with serious illnesses, help patients live longer, and reduce healthcare costs. The document proposes developing a palliative care program at HealthAlliance Hospital through a team approach and various models of consultative and inpatient palliative care services.
This document summarizes the key priorities and recommendations from the Five Year Forward View for Mental Health (5YFV MH) report in the UK. The 5YFV MH aims to transform mental health services by 2020 through four priorities: 1) Improving 24/7 crisis care, 2) Integrating physical and mental health care, 3) Promoting good mental health, and 4) Reforming the mental health system. Some recommendations include expanding 24/7 crisis services, increasing access to psychological therapies, and developing children's crisis models. The 5YFV MH dashboard will monitor progress through key metrics on areas like crisis care, perinatal services, and outcomes for people with mental health problems.
This document discusses mental health as a global priority and outlines reasons for investing in mental healthcare. It finds that up to 10% of people worldwide are affected by mental health problems, which represent the 5th leading cause of disease burden globally when measured in disability-adjusted life years. However, most low- and middle-income countries allocate less than 2% of their health budgets to mental health. Compelling reasons to invest in mental healthcare include promoting human rights, reducing human and economic costs, and implementing cost-effective treatment solutions that already exist.
Parallel Session: Engaging Patients: The New Blockbuster DrugNHSScotlandEvent2013
In this session, Maureen Bisognano, President and CEO of the Institute for Healthcare Improvement (IHI), shares the latest tools to engage patients and families in the care system. Many are calling person-centred care/patient engagement ‘the next blockbuster drug’ because of its powerful potential to produce the best outcomes while learning best practices.
See more on the 2013 NHSScotland Event website http://www.nhsscotlandevent.com/resources/resources2013/resources
LifeCourse: An Innovative Approach to Late Life Care in the CommunityAllina Health
LifeCourse is an innovative approach to providing late life care in the community developed by Allina Health. It aims to improve quality of life for seriously ill patients and their families by providing whole person care through regular in-home visits from lay healthcare workers. Early results show LifeCourse may help maintain patients' quality of life while reducing healthcare costs by decreasing hospital and emergency room use in the last years of life. Allina Health is expanding the program and evaluating outcomes to determine its long-term impact.
Angela Coulter and Beverley Matthews presented a webinar on why care planning is not happening widely in the NHS. They discussed how care planning can help patients better manage their long-term conditions through shared goal setting and action planning. However, surveys show that less than 10% of patients with long-term conditions have a written care plan. Barriers to effective care planning included a lack of time and resources, inflexible systems, and a clinical culture that does not prioritize self-management support and partnership with patients. The webinar argued that improving care planning requires addressing attitudes, skills, leadership and incentivizing planning through policies and performance measures.
The document provides an introduction to palliative care and a holistic approach. It defines palliative care according to the WHO as improving quality of life for patients facing life-threatening illness through preventing and relieving suffering. Key principles of palliative care discussed include taking a holistic, patient-centered approach and using a multidisciplinary team. Factors affecting provision of palliative care and strategies for improving services are also outlined.
MHM Roundtable Slide Deck WHA Side-event May 28 2024.pptx
Caring for Carers
1. Spring 2015
Caring for Carers
An analysis of carer therapy provisionin the
Centre for Health and Well Being
Kate Laverty, Angie Shen, Chioma Iwelumo
2. 2
Table of Contents
Foreword.....................................................................................................................................3
Rationale......................................................................................................................................4
Context........................................................................................................................................5
CHWB ......................................................................................................................................5
Literature Review...................................................................................................................... 6
Complementary Therapies in the United Kingdom...................................................................6
Mental Healthin the UK ........................................................................................................6
Carers in the UK .................................................................................................................... 7
Methodology................................................................................................................................ 9
Sample.....................................................................................................................................9
Survey......................................................................................................................................9
Bias........................................................................................................................................ 10
Findings ..................................................................................................................................... 12
Demographics..................................................................................................................... 12
Category of Care ................................................................................................................. 14
Types of Care...................................................................................................................... 16
Time Commitments............................................................................................................. 18
Challenges.......................................................................................................................... 22
Mental HealthNeeds........................................................................................................... 24
Additional Support.............................................................................................................. 28
Motivation for Services........................................................................................................ 30
Usefulness of Services ......................................................................................................... 31
Discussion.................................................................................................................................. 35
Recommendations...................................................................................................................... 36
Conclusion ................................................................................................................................. 37
Bibliography............................................................................................................................... 38
Appendix.................................................................................................................................... 39
Appendix I Raw Data from Survey............................................................................................ 39
3. Foreword
It gives me great pleasure to present this research which outlines the needs and challenges
of carers and show cases the work our centre does to meet these needs. It evinces further
investment is needed though to ensure the inspiring work of carers continues without
causing harm to those caring for their loved ones.
From 2012, the Centre has provided therapies to 17 men and 111 women with investment
from BHSCT. We have delivered therapies to a further 45 men and 212 women through
philanthropic funding. These clients have either received the allocated interventions from
BSHCT or are not registered as carers and therefore unentitled to the therapies offered by
BHSCT to registered carers.
This research was conducted with 85 of the BHSCT funded clients. 89% of respondents were
women, roughly mirroring the diversity in gender of referrals where women make up 86.7%
of the BSHCT referrals.
The mean age for the 128 BHSCT referrals was 56 for women and 54 for men. The mean age
for the 85 respondents was 52 for women and 57 for men. Key findings include;
47% of our carers care for older people
Emotional support and household tasks are the most common help provided
55% of our carers care for more than 100 hours
95% of challenges faced by our carers are emotional ones
65% of carers receive no formal support
42% of our carers felt respite care would be the most beneficial support they could
be offered
89% of carers suffer stress and worry
80% of our carers said complementary therapies brought stress relief
69% of our cares were referred by a social worker
62% of carers felt the services were helpful
86% felt the service in the Centre was ‘excellent’
7% felt they would not have been able to afford a donation of £5 per hour if it had
been sought
4. Rationale
Buildingoncentre specificresearchinrecentyearsaboutthe perceptionof therapiesandtheir
usefulnesstoclientsinthe UpperSpringfieldarea,thisreportaddressesthe specificneedsof a
particulardemographicwithinourclientele. This research aims to study the mental health
needs and daily challenges of the carer demographic among the clientele of Centre for
Health and Wellbeing and how the complementary and alternative therapy the Centre
provides caters to their needs.
The rationale for undertaking the research was three-fold:
1. To gain a better understanding of the challenges facing carers in Northern
Ireland, particularly their mental health problems and needs.
2. To gain a better understanding of the carer clientele at the Centre for Health
and Well Being, particularly why and how they utilize and experience the
Centre’s service.
3. To assess the effectiveness of the Centre’s service in addressing carers’
mental health needs, and determine how to better serve the carer clientele.
5. Context
CHWB
The Centre for HealthandWellbeinghasdeliveredcomplimentarytherapies throughoutWest
Belfastfor17 years. We offereachclient6 one hour longtherapies,one perweekatthe same time
each weekfor6 weeks,afterwhichtime theywill have devisedapersonal developmentplanalong
withtheirtherapistandoutcomesshouldreflectimprovedmental andphysical health. We have 2
staff,3 volunteersand6 boardmembersaswell as2 volunteercounsellorsand10 self employed
therapists.Ourvolunteersare local peoplewhohave benefittedfromthe servicesprovidedand
wantto give somethingback.Twoof our therapistsare alsopast clientswhohave completed
accreditedtrainingwithusandenhancedtheirlearningwithaminimumof 50 CPD hoursper annum
overthe last 7 years.Nowself employed,theyare contributingtothe economy.
6. Literature Review
Systematicliteraturesearcheswereperformedusingseveraldatabases,reference listsearching,and
inquirytocolleagues.
Complementary Therapies in the United Kingdom
Complementary therapies are becoming more popular
and widespread with rising numbers of people using
them in conjunction with conventional western
medicine. In order to serve the community and its
needs, it is important to study the effectiveness of
complementary therapies in order to maximize its positive benefits for those receiving
treatments.
With 32 million visits in 2008 in England, one in ten people aged 60 to 74 living in private
households in Great Britain had a common mental disorder (such as anxiety, depression and
phobias) according to the Stationary Office. Occurrence in older age groups declined, and
were more commonly reported by women than men. The NHS provided an estimated 10%
of these. The majority of non-NHS visits were financed through direct out-of-pocket
expenditure estimated at £450 million. The findings suggest that therapies are making a
measurable contribution to first-contact primary care. Herbalism, aromatherapy,
homoeopathy, acupuncture/acupressure, massage and reflexology were the most popular
treatment modalities. The main reasons for trying
complementary therapies were due to its perceived
effectiveness, a positive inclination towards it, and its relaxing
effects. On average, users spent £13.62 on therapies per
month, which extrapolates to an annual expenditure of £1.6
billion for the whole nation.
Mental Health in the UK
Mental healthhasan importantimpacton all aspectsof ourlivesatindividual,communityand
societal levels.Poormental healthcontributestosocio-economicandhealthproblemssuchas
higherlevelsof physical morbidityandmortality,lowerlevelsof educational attainment,poorer
workperformance,greaterincidence of addictions,highercrime ratesandpoorcommunityand
societal cohesion (Goldie&McCulloch,2010).
Mental ill-healthcanhave diverse andlong-termeffectsonindividuals,familiesandsociety.The
Office forNational StatisticsPsychiatricMorbidityreportfoundthatinanyone year 1 in 4 British
adultsexperience atleastone mental disorder (Singleton,etal.,2001), and 1 in6 experiencesthisat
any giventime.Mixedanxietyanddepressionisthe mostcommonmental disorderinthe UK,with
almost9% of people meetingcriteriafordiagnosis (Singleton,etal.,2001). The core symptomsare
lowmood,fatigue orlack of energy,lackof interestorenjoymentinlife (Halliwell,etal.,2007).
Anxietyischaracterisedbyworryandagitation,fatigue(restlessness)andstress (Halliwell,etal.,
2007).
Womenare more likelytohave beentreatedforamental healthproblemthanmen(29% compared
with17%) (National Statistics,2003).Depressionismore commoninwomenthanmen.1 in 4
7. 7
womenwill require treatmentfordepressionatsome time,comparedwith1in10 men (NHS,2003).
Womenare twice aslikelytoexperience anxietyasmen (Singleton,etal.,2001). Overall,common
mental healthproblemspeakinmiddleage.Olderpeople are lesslikelytohave acommonmental
healthillnessthanothersectionsof the Britishpopulation (Singleton,etal.,2001). However,
depressionaffects1in5 people overthe age of 65 livinginthe communityand2 in5 livingincare
homes. (Baldwin,2002) Accordingto the HealthSurveyNorthernIreland2013/14 conductedby
Departmentof Health,Social ServicesandPublicSafety (Walker,etal.,2014) one-fifthof
respondents(19%) showedsignsof apossible mental healthproblem(GHQ12score ≥4). This was
true for more females(20%) thanmales(16%).Youngfemales(aged16-24 yearsold) were more
likelythanyoungmalestohave showedsignsof apossible mental healthproblem(23% compared
with13%).
While these statistics show the prevalence of mental health issues at large, this report will
focus on the almost 214,000 carers in N. Ireland. A carer is anyone who cares, unpaid, for a
friend or family member who due to illness, disability, a mental health problem or an
addiction cannot cope without their support. According to the 2011 Census, 6.5 million
people in the UK are carers, about 10.3% of the population, an 11% rise in the number of
carers since the last Census in 2001. 58% of carers are female and 42% are male. The
majority of carers are of working age and the peak age for caring is 50-64 – 1 in 5 people in
this age bracket are carers. The care provided unpaid, by the nations’ carers is worth an
estimated £119bn per year – considerably more than total spending on the NHS (Carers UK;
University of Leeds, 2011).
Carers in the UK
The causes of someone taking on caring
responsibilities are varied but can include serious
physical illness, long-term physical disability, long-term
neurological conditions, mental health problems and
learning difficulties. The 2011 Census shows that
caring tends to affect men and women at different
times. Women are much more likely to care in middle
age. 1 in 4 women aged 50-64 have caring
responsibilities, compared to 1 in 6 men. Women have a 50:50 chance of providing care by
the time they are 59; compared with men who have the same chance by the time they are
75 years old. The imbalance reduces amongst older carers and men are slightly more likely
to provide care than women amongst retired people– many caring for their partners.
The 2011 Censusalsoshowsthatthere were 213, 980 carers inNorthernIreland,a16% increase
fromthe numberof carers in2001. The greatestincreases(21%) were amongthose caringforover
fiftyhoursa week. 26% provided50or more hoursper weekof care.57% providedless than20
hoursof care perweek.Inthe 2009/10 NHSsurveyconductedinEnglandandWales (NHS
Information Centre, 2010), 52% of carers cared forlessthan 20 hoursof care a week.22% cared
for 20-49 hours a week.9%cared for 50-100 hours a week.13% cared for 100 hour or more.1 71% of
1 The 2009/10 NHS survey noted that its methodology produced a more modest prevalenceof lower-intensity
caring,especially away fromthe home.
8. 8
those whocare for lessthan20 hoursa weekreporttheirhealthasgood,whereasonly52% of
those whocare more than 20 hoursa weekreporttheirhealthasgood. Half of carers (50%) they
were affectedbydepressionaftertakingona caring role.The 2009/10 NHS surveyalsofound
differencesinmental healthsymptomsexperiencedbycaresintermsof genderand hoursof care
providedperweek.More womenexperience all of the symptomsthanmen: tiredness(39%
comparedto 25%), stress(34% comparedto22%), disturbedsleep(28% comparedto21%),short
temper(24% comparedto19%) and depression(21% comparedto15%). Carerswhoprovide more
than 20 hoursof care are significantlymore likelytoexperience mental healthsymptomsthanthose
whoprovide lessthan20 hours of care: tiredness(47% comparedto25%), stress(38% comparedto
22%), disturbedsleep(35%comparedto16%), shorttemper(26% comparedto 18%) and depression
(25% comparedto 12%).
Cares’ duties are varied and include practical household tasks such as cooking and cleaning,
personal care such as bathing and dressing, and emotional support such as offering advice
and friendship. In the 2014 CarersUK State of Caring Survey (Carers UK, 2014), 93% of
carers said they provide practical help such as preparing meals, doing laundry or shopping.
87% provide emotional support, motivation or keeping an eye on someone either in person
or by phone. 71% of carers provide personal care like help with washing, dressing, eating or
using the toilet. 57% carers provide physical assistance – getting in and out of bed, moving
around or getting out of the hour.
The 2013 InSicknessandinHealthsurvey(CarersUK,et al., 2013) askedcarers to identifywhathad
impactedontheirphysical andmental health.A lackof practical supportwas a reasonfor 64 per
centof carers and 50 percent saidtheydonot have enoughfinancial support.Meanwhile 67per
centof carers whorespondedtothe surveysaidtheydidnothave enoughemotionalsupport.
Carersthoughttheirhealthwouldbe improvedbymore regularbreaksfromcaring(61%).financial
support(52%).more advice and information(43%).practical supportsuchascare workers and
domestichelp(52%). The 2009 survey found that, as a result of carers assessment or review,
carers receivedservicesforthe caredperson(22%),informationaboutsupportgroup(16%),break
away fromhome (8%).33% didnot receive anyservices.
9. Methodology
Data extractionfollowedapredefined protocol. Clientswere invitedonarrival tothe centre,or by
telephonetorespond.
Sample
The sample populationisthe carerclientele atthe Centre from2012 to 2015 who have been
referredbythe BHSCT and have at leastcompletedone sessionof treatment.A total of 113 carers
visitedthe Centre from2012 to2015; 85 of them(75%) respondedtothe survey.
Survey
The data for the client portion of this project was collected via an anonymous 14-question
survey (Appendix I). The survey remained anonymous so that the most honest answers may
be obtained. All questions, except for the responder’s age, are multiple-choice questions.
A majorityof the responseswere collectedviatelephone callsconductedbyatemporaryinternwith
no pastor long-termtiestothe Centre.Informedconsentwasobtainedandthe surveyquestions
were readverbatim.Responseswere loggeddirectlyintothe online surveysoftware Qualtrics. The
intern made multiple attempts to reach every client on file, calling back unanswered
numbers on different days at different times of both day and evening. The hardcopy version
of the surveywasadministeredtocurrentclientswhoare carers,available atthe Centre uponarrival
for a scheduledappointment.Responseswere manuallyenteredintothe online surveyby
researchersaftercompletion.
There are several advantagesof usingsurveysasa data collectiontool.Large amountsof
informationcanbe collectedfromalarge numberof people inashort periodof time andina
relativelycosteffective way.The resultsof the surveycanusuallybe quicklyandeasilyquantifiedby
eitheraresearcheror throughthe use of a software package.Whendatahas beenquantified,itcan
be usedto compare and contrast otherresearchandmay be usedto measure change (Ackroyd&
Hughes,1981). In thiscase,surveyhasbeenchoseninorderto collectinformationfromcarers,to
quantifythe datausingQualtricsandto findcorrelationsbetweendifferentfactorsunderstudy.
Cross-tabulationisusedtoexamine how twodifferentvariablesare relatedtoeachother.
10. Bias
Several potential sources of bias have been identified, and measures have been taken to
mitigate their effects.
Type of Bias Relevance toProject MeasuresTakento Avoidbias
Acquiescence bias:
respondents have atendencyto
agree withall the questionsin
a measure due to the motivation
to be agreeable toplease the
researcherorto save time.
(Watson, 1992))
Respondentsmayinaccurately
reportthe helpfulnessof therapy
(See Question9inAppendix I) or
agree withthe potential positive
effectsof therapy(See Question
10)
1. A vast majority (90.6%) of
respondents have
completed their treatment
and have no long term ties
to the Centre.
2. Scales of 1-5 were used to
enable respondents to
express their attitudes
more accurately
3. Respondents were assured
before the survey that it
would take less than 5
minutes, so that they were
more likely to ponder over
their answers
Social desirability bias:
respondents have a tendency
to deny undesirable traits to
make themselves look more
favourable to the researcher
(Furnham, 1986)
Respondentsmaybe unwillingto
admitto mental healthissues
(See Question7inAppendix I).
Individualswithmental disorders
are more likelytodecline
participationandlesslikelyto
reportstigmatizingsymptoms,
leadingtoan underestimationof
prevalence andtreatment
figures. (Knauper & Wittechen,
1994) Clientsare more likelyto
overreportthe numberof hours
care theygive perweek,equating
‘livingwith’the personto‘caring
for’the person.
1. Choices were edited to be
as neutral as possible. For
example, Question 7 asks
for mental health
symptoms rather than
problems. Behaviours such
as drinking and smoking
were not asked.
2. Respondents were assured
the survey is anonymous.
3. Respondents were told
that the purpose of the
survey is to learn about
challenges facing carers
and to improve services for
carers.
4. Respondents were asked
to consider only the hours
they actually completed
daily tasks for those for
whom they cared, negating
the hours in which they
simply lived in the same
house.
Non-response bias:respondents
differinmeaningful waysfrom
nonrespondents
Clientswhodidnotrespondto
the surveyare more likelytobe
those who(1) hada negative
1. Multiple attempts were
made to reach those who
did no answer their phones
11. 11
experience atthe Centre;(2)
were unable to answertheir
phonesbecause the personthey
care for needsintensive care;(3)
are inpoor mental orphysical
healthcondition
2. The researcher will take
the potential influences of
such biases into account
when performing analysis
of the responses.
12. Findings
Demographics
89% of surveyrespondentsare female. 86.7% of all BSHCT referralsare female,roughlymirroring
the percentage of female respondents(89%) of the survey. Inthe UK, 58% of cares are female. The
meanage forthe 85 respondentswas52for womenand57 for men. The meanage for the 128
BHSCT referralswas56 forwomen(4 yearsolderthanthe meanage of respondents) and54 for men
(3 yearsyoungerthanthe meanage of respondents).The mostcommonage groupis 50-59 year old,
concurrentwiththe respondents.
Figure 1: Age Distribution
Disproportionatelymore women (89%) were referredtoourcentre andtook upthe offerthanmen,
considering58%of carers are female and42% are male accordingto the 2011 UK Census.Thiscan
be accountedfor bythe followingfactors.First,womenare more likelytoexperience mental health
problems.Second,womenare more likelytoseektreatmentthanmen.Third,womenare more
likelytorespondtomental healthsurveys.
All of the respondentswhocare fortheirfamilyandchildrenandthose withalearningdisabilityare
women. Men(55%) are more likelytocare for an olderpersonthanwomen(45%). Men (33%) are
more likelytocare for a personwithphysical disabilitythanwomen (20%).
All menprovide personal care.Menare more likelytoprovide physical assistance thanwomen.
Womenare more likelytoprovide emotional supportthanmen.Womenare more likelytoassist
withhouseholdtasksthanwomen.
Women(96%) are more likelytoreportemotional challengesthanmen(89%).Men(56%) are more
likelytoreportphysical challengesthanwomen(49%).
Womenare more likelytoreporthavingexperiencedall of the mental healthsymptomsthanmen
exceptforpoorsleep.
Women(71%) are more likelytohave beenreferredbyasocial workerthan men (56%).Men (33)
are more likelytoreport thattheyneededhelpforcoping thanwomen(11%).
Two womenreported the therapieswereslightlyhelpful andanothertwowomenreportedthe
therapieswere notatall helpful.Womenare more likelytoexperience all of the mental health
benefitsof therapythanmen.
0
10
20
30
20-29 30-39 40-49 50-59 60-69 70-79 80-89
Age Distribution of Survey Respondents
13. 13
Women(29%) are more likelytonothave receivedanyinterventionthanmen(11%).Men(22%) are
twice as likelytohave receivedrespite care aswomen(11%).Women (29%) are more likelytothink
no additional servicescouldimprove theirsituationthanmen(11%). Men(78%) are more thantwice
as likelytohave receivedrespite care aswomen(38%).
The male respondents(mean=57) inthe sample are olderthanthe female respondents(mean=53).
Those who care for an olderperson(mean=57) are to be olderthan average.Those whocare for
theirfamilyandchildren(mean=39) or someone withlearningdisability (mean=48) are youngerthan
average.
Those whoprovide care for more than 100 hours a week(mean=58) are olderthanaverage.
Those whoreportphysical challengesasone of the biggestchallenges(mean=57) are olderthan
average.Those whoreportfinancial challengesasone of the biggestchallenges(mean=48) are
youngerthanaverage.
Those whohave experiencedlackof enjoymentinlife (mean=57) are olderthanaverage.
Those whoneededtime forself (mean=49) are youngerthanaverage.
Those whorated the therapiesasextremelyhelpful (mean=58) are olderthanaverage. Those who
didnot experience any relief of symptoms(mean=59) are olderthanaverage. Those who
experiencedasense of wellbeingare olderthanaverage.
Those whoare not receivinganyadditionsupport(mean=57) are olderthanaverage.Those whoare
receivinghome help(mean=59) are olderthanaverage.
Those whorated the qualityof service asgood (mean=49) are youngerthanaverage. Those who
ratedthe qualityof service asaverage orpoor (mean=58) are olderthanaverage.
Those whoreportedthattheyare moderatelylikelytopay5 poundsfora session(mean=64) are
olderthanaverage.Those whoreportedthattheyare notat all likelytopay5 poundsfora session
(mean=45) are youngerthanaverage.
14. Category of Care
Almosthalf of
respondentscare for
an olderperson
(50%).22% care for
a personwith
physical/sensory
disability (16%).
15% care fora
personwithmental
healthproblem
(14%).12% care for
a personwith
learningdisability
(5%).6% care for
theirfamilyand
children (2%).
The figures in blue
above indicate the
figures for the
categories of care reported in the 2015 BHSCT carers assessment report. According to
January-March 2015 Quarterly Carers’ Statistics for Northern Ireland, the majority (50%) of
carers who had been offered an assessment during quarter ending 31 March 2015 were
caring for someone in the Older People client group. The client group with the least offers of
a carers’ assessment was Family and Child Care (2%).
It would seem we see disproportionately high numbers of peple caring within the categories
of ‘learning disability’ and ‘family and children’ and low numbers of those caring ith in the
category of ‘physical disability’.
All of the respondentswhocare fortheirfamilyandchildrenandthose withalearningdisabilityare
women.Men(55%) are more likelytocare for an olderpersonthanwomen(45%). Men (33%) are
more likelytocare for a personwithphysical disabilitythanwomen(20%).
Consideringthe meanage withineachcateogry,there are notabledifferenceswiththe youngest
carers reportedinthe category‘familyandchildren’.Those whocare foran olderperson(mean=57)
are to be olderthanaverage.Those whocare fortheirfamilyandchildren(mean=39) orsomeone
withlearningdisability(mean=48) are youngerthanaverage.
Table 1: Category of Care
Category Older
Person
Learning
Disability
Physical
Disability
Mental
Health
Family And
Children
Mean
age
55 48 54 51 39
All of those whocare for someone withlearningdisabilityprovidepersonalcare andemotional
support.All of those whocare fortheirfamilyandchildrenprovidepersonalcare.
Figure 2: Category of Care
15. 15
90% of those whocare for someone withlearningdisabilitycare formore than10 hours a week,
comparedto 38% of those whocare for someone withmentaldisabilityand44% of those whocare
for an olderperson.All those whocare forsomeone withlearningdisabilitycare formore than 50
hoursa week.
Those whocare for theirfamilyandchildrenare more likelytoexperience all three challengesthan
those whoprovide othercategoriesof care.All of those whocare for someone withlearning
disabilityorthose whocare fortheirfamilyandchildrenexperienceemotional challenges.
100 percentof those whocare fortheirfamilyandchildrenexperience fatigue.Those whocare for
someone withphysicaldisabilityare mostlikelytoexperience lackof enjoymentinlife(72%)
comparedto those whocare fortheirfamilyandchildrenwhoare leastlikelytoexperience lackof
enjoymentinlife (40).100% of those whocare for someone withmental disabilityandthose who
care for theirfamilyandchildrenexperience stress.100% of those whocare for someone with
learningdisabilityandthose whocare for theirfamilyandchildrenexperience poorsleep.
Those whocare for someone withleaningdisability (20%) andthose whocare fortheirfamilyand
children (20%) are most likely tohave neededhelpforcopingcomparedtothose whoprovide other
categoriesof care.Those whocare for someone withlearningdisabilityare mostlikelytohave
wantedtime forself (50%) comparedtothose whoprovide othercategoriesof care.Those whocare
for theirfamilyandchildrenare mostlikelytohave wantedrelaxation(60%) comparedtothose who
provide othercategoriesof care.
100 percentof those whocare fortheirfamilyandchildrenratedtherapyasextremelyhelpful. 100
percentof those whocare for theirfamilyandchildrenexperienced relaxation.Interestingly,those
whocare for someone withmental disabilityare mostlikelytoexperience improvedqualityof life
(38%),sense of wellbeing(62%),happier(62%) andlesspain(46%) comparedto those whoprovide
othercategoriesof care.Those who care for someone withtheirfamilyandchildrenare leastlikely
to experience improvedqualityof life (0%),sense of wellbeing(20%),happier(20%) andlesspain
(0%) comparedto those whoprovide othercategoriesof care.
Those whocare for someone with learningdisability are mostlikelytonothave receivedany
treatment(90%) comparedto those whoprovide othercategoriesof care.Those whocare for their
familyandchildren(40%) are leastlikelytonothave receivedanytreatmentcomparedtothose who
provide othercategoriesof care.Of those whocare forsomeone withlearningdisability,noone
receivedhome helporcounselling.Of those whocare forsomeone withmental healthproblemand
familyandchildren,noone receivedhome help.
Remarkably, 40%of those whocare forsomeone withlearningdisabilityreportedthatfinancial
supportcouldbe helpful,comparedto21% of those whocare for an olderperson,22% of those who
care for someone withphysical disability,23% of those whocare for someone withmental disability
and 0% of those whocare for theirfamilyandchildren.
16. Types of Care
Respondents provide personal care (79%, compared to 93% in the CarersUK survey from
2014), physical assistance (79% compared to 57% in the CarersUK survey from 2014),
household help (86%) and emotional support (86%). Household tasks was the most
common type of care offered by women and the least common type of care offered by men.
Figure 3: Areas of Care
Thiscross tabulation overleaf outlineswhatdutiesare conductedbyrespondentsineachcategoryof
care. The rows inred give the count fora combinationof valuesof the twovariables.Forexample,
30 respondents bothcare foran olderpersonandprovide personal care. The rowsinorange display
the counts as percentagesof eachof the columns. Forexample,75% of those whocare for an older
personprovide personal care. Consideringthe typesof care providedwithineachcategory,the table
belowoutlinesthe differenceswithinthe population. 75% of people whocare forolderpeople
provide personal care,althoughthe greatesthelpisrequiredincompletinghouseholdtasksand
providingsupporttoolderpeople. All thosewhocare forsomeone withalearningdifficultyhave to
provide personal care suchas washinganddressingaswell asprovidingemotionalsupport. A
remarkablyhighnumberof people whocare forthose withmental health needsare offering
physical supports –76.92%. It is notsurprisingthattheyare providingpredominatelyemotional
support– 84.62%, butthat that the same percentage are alsodoinghouseholdtaskssuchascooking
isalso striking.
79% 79%
86% 86%
75%
80%
85%
90%
personal care physical asistance household tasks emotional support
Types of Care
17. 17
Table 2: Cross Tabulation--Category of Care & Areas of Care
3. What category of disability does the person you are caring for
belong to?
older
person
learning
disability
physical/
sensory
disability
mental
health
family
and
children
Total
4. What
are your
main
responsibil
ities?
personal care 30 10 13 11 5 67
75 100 68.42 84.62 100 78.82
physical
assistance
31 9 16 10 3 67
77.5 90 84.21 76.92 60 78.82
emotional
support
35 10 16 11 3 73
87.5 100 84.21 84.62 60 85.88
other 3 0 0 1 0 4
7.5 0 0 7.69 0 4.71
household
tasks
36 7 17 11 4 73
90 70 89.47 84.62 80 85.88
Total
40 10 19 13 5 85
100 100 100 100 100 100
18. Time Commitments
More than half of respondents
(55%) provide more than100
hoursof care a week.The same
percentage (18%) provide 20-50
and 50-100 hoursof care per
week.9% of respondents
provide lessthan20 hours of
care perweek. Comparedto
respondentsof the 2009/10
NHS survey,carerswho
respondedtooursurvey
provide significantlymore hours
of care.Carers whoresponded
to our surveyare fourtimes
more likelytocare for more
than 100 hours (55% comparedto 13%) andalmost6 less likelytocare forlessthan20 hours (9%
comparedto 52%). The 2009/10 NHS survey alsofoundthat those whocaredfor more than 20 hours
perweekwere twice aslikelyasthose whocaredforlessthan20 hours perweektofeel tired,1.5
timesmore likelytofeelstressed,twiceaslikelytohave disturbedsleeptofeel depressedand1.7
timesaslike tobe shorttemperedandirritable. 90% of BSHCT referralstoour centre cared for
more than 20 hoursper week,speakingtothe veryreal possibilityof thispopulationpresentingwith
level,complex andmulti-facetedneeds.The NHSsurveyalsofoundthatwomenreportedhigher
instancesof tiredness,stress,insomniaanddepressionthanmenbyas muchas 13%.
It isimportantto considerif a particularcategoryof care requiresahighertime commitmentthan
the others. Each categoryof care had the same trend;the leastreportednumberof carerswere in
the ‘lessthan20 hours’bracketand the greatestamountof carers were inthe ‘more than100 hours’
bracket. 36% of those caring for an olderpersoncare formore than100 hoursper weekcompared
to only6.4% of those whocare withinthe ‘familyandchildren’section. Peoplecaringforthose with
physical andmental healthneedsare mostlikelytocare forlessthan 20 hours,but47 of the 85
respondentscare forsomeone formore than100 hours perweek. UsingUK figuresforcalculation,
N.Irelandcarers provide £3.9 billionof care2.
Emotional support provided for between 50-100 hours was the most common modality of
care provided (93.33%). Those caring for more than 100 hours tended to provide physical
assistance (91.49%) and emotional support (91.49%). Women were more likely than men to
provide high-intensity (more than 20 hours a week) care (62% compared with 38%); 19 %
were aged 45-54 and 18 % were aged 55-64 and 30% were aged 65 or over.
2 £119 billion of careprovided by 6.5 million carers,214,000 of whom are in N. Ireland x £minimum wage
(£6.50, 2015)
Figure 4: Time Commitents
19. 19
Figure 5: time commitment & challenges
The figure above shows that the percentage of people who experience physical and financial
challenge generally increases with the amount of time people spend caring.
Table 3: Cross Tabulation--Time Commitment & Category of Care
5. How much time do you spend caring each week?
Less than
20 hours
20-50
hours
50-100
hours
more
than 100
hours
Total
3. What
category
of
disability
does the
person
you are
caring for
belong to?
older person 6 7 10 17 40
75 46.67 66.67 36.17 47.06
learning disability 0 0 1 9 10
0 0 6.67 19.15 11.76
physical/sensory
disability
1 3 2 13 19
12.5 20 13.33 27.66 22.35
mental health
problem
1 4 3 5 13
12.5 26.67 20 10.64 15.29
family and
children
0 1 1 3 5
0 6.67 6.67 6.38 5.88
Total
8 15 15 47 85
100 100 100 100 100
0
20
40
60
80
100
120
Less than
20 hours
20-50
hours
50-100
hours
more than
100 hours
percentageofpeople time committment & challenges
emotional challenges
(e.g. social isolation,
stress, worry)
physical challenges
(e.g. back pain,
tiredness)
financial issues (e.g.
work care balance)
20. 20
Figure 6: time commitment & mental health symptoms
The above graph shows the general trend that the percentage of people who experience
mental health symptoms generally increases with the amount of time people spend caring.
A vastmajority(82%) of those whosoughttreatmentbecause theyneededhelpwithcopingprovide
care for more than100 hoursa week.The more hoursof care carers deliver,the more likely carers
soughttreatmentbecause theyneededrelaxation.The same holdstrue forthose whosought
treatmentbecause theyneededhelpwithcoping.Noone whoprovidescare forlessthan20 hoursa
weeksoughttreatmentbecause theycouldn’tcope,comparedto 19% of those whocare for more
than 100 hours a week,7%of those whocare for 50-100 hoursa weekand7% of those whocare for
20-50 hoursa week.We see the opposite trendforthose whowere referredbytheirGPs.25% of
those whocare for lessthan20 hourswere referredbytheirGPsbutonly% of those whocare for
more than 100 hourswere referredbytheirGPs
100% of those whoprovide care for50-100 hoursexperiencedrelaxation.Those whocare formore
than 100 hours a weekare leastlikelytoexperienceimprovedqualityof life andlesspaincompared
to those whocare for fewerhours.
0
20
40
60
80
100
120
0 1 2 3 4 5
percentofpeoplewhoexperiencethe
symptom
Hours of care provided per week
low mood
fatigue or lack of energy
lack of enjoyment in life
stress and worry
frustration and anger
poor sleep
restlessness
21. 21
Figure 7: time commitment & additional support received
The above graph showsan increasingtrendof the percentage of peoplewhoreceive respite care
withthe amountof time spentcaring.Italso showsa decreasingtrendof the percentage of people
whoreceive counsellingandhome help.
0
10
20
30
40
50
60
70
80
Less than 20
hours
20-50 hours 50-100 hours more than
100 hours
percentageofpeople time commitment & additional supprt
received
none
counseling
respite care
peer support groups
home help
22. 49%
95%
26%
0%
20%
40%
60%
80%
100%
physical
challenges
emotional
challenges
financial
challenges
Challenges
Challenges
Seekingtodetermine if our
respondentsself-identifiedany
physical,emotional orfinancial
challenges,we foundthat95% of
respondentsexperience emotional
challenges.49%of respondents
experience physical challenges.26%
of respondentsexperience financial
challenges. More women(96%) than
men(88%) reportedemotional
challenges.
Thismimicsfindingsfrom multipleUKsurveys.
Seekingtodetermine if there wasacorrelationbetweenthe numberof hourscaredand the typesof
challengesperceivedbycarers,we crosstabulatedthe resultsfrombothresponses. Those who
cared forlessthan100 hoursall reportedfeelingsof isolation,stressandworry. Those whocared
for lessthan20 hoursper weekreportednofinancialconcerns,comparedto34% of those caring
more than 100 hoursperweek. Interestingly,there wasadipinthe reportingof physical challenges
for those caringbetween50-100 hoursper weekfromthose caringbetween20-50hours perweek
and those caringmore than 100 hoursperweek.
Table 4: Cross Tabulation--Time Commitments & Challenges
5. How much time do you spend caring each week?
Less than
20 hours
20-50
hours
50-100
hours
more than
100 hours
Total
6. What
is(are) your
biggest
challenge(s)
as a carer?
emotional
challenges 8 15 15 43 81
100 100 100 91.49 95.29
physical
challenges 2 8 6 26 42
25 53.33 40 55.32 49.41
financial
issues 0 3 3 16 22
0 20 20 34.04 25.88
other 0 1 0 2 3
0 6.67 0 4.26 3.53
Total
8 15 15 47 85
100 100 100 100 100
Those who experience financial challenges are more likely to experience lack of enjoyment
in life (64%) compared to those who experience physical (54%) and mental challenges
Figure 8: Challenges
23. 23
(50%). Those who experience financial challenges are more likely to experience restlessness
(59%) compared to those who experience physical (46%) and mental challenges (45%).
After therapy, those who experience financial challenges (14%) are less likely to have
experienced improved quality of life than those who experience physical (25%) and mental
challenges (24%). Those who experience financial challenges (18%) are less likely to have
experienced less pain than those who experience physical (27%) and mental challenges
(24%).
Those who experience financial challenges (41%) are much more likely to report that
financial support could be useful compared to those who experience physical (24%) and
mental challenges (29%).
Those who experience financial challenges are less likely to pay 5 pounds for a session of
therapy. 18% of those who experience financial challenges are not at all willing to pay,
compared to 6% of those who experience physical challenges and 10% of those who
experience mental challenges
24. Mental Health Needs
In the 2009 survey,awide range of effectswere mentioned;34% of carers reportedfeelingtired,29
% feltstressed,25% haddisturbedsleep, 22 % reportedbeingshorttemperedorirritable,19% felt
depressed.Inthe 2013 survey, 83%of carers statedthat caringhas had a negative impactontheir
physical healthand87 per centof carers statedthatcaring has had a negative impactontheir
mental health.Carers were affectedinthe followingways:abitor a lotlessof sleepasa resultof
caring (52%) , anxietyorstress(91 percent),depression(53percent).The 2014 surveyfoundthat
over80% of carers reportthat caring has a negative impactontheirhealth.69% reportdisturbed
sleepbecause of caring.73% of carers surveyedreportingincreasedanxietyand82% increased
stresssince takingontheircaring role.
While an equal number of men and women reported restlessness, 73.68% of women
reported low mood compared to only 55.56% of men. The biggest difference though is in
stress and worry where 93.47% of women and 55.56% of men reported it.
Other Comments
Got usedto the stressand fatigue;tryto notreveal frustrationtohusband(hercaree)
No job
My Kidskeepme going
Sufferfromanxiety
Cry a lot
Had a breakdown
Figure 9: Mental Health Symptoms
For women who answered the question “What mental health symptoms, if any, have
you experienced?” about 93% said that stress and worry were one of them, 88% said
fatigue or lack of energy is one, and 85% said poor sleep was another. For men that
answered the question, about 89% said that poor sleep was a symptom and 78% said
that fatigue or lack of energy was another.
For carers that are caring for an older person, about 88% included fatigue or lack of
energy as a symptom. Of carers caring for someone with a learning disability, all of
them reported poor sleep as a symptom. Of carers responding that they care for
persons with a physical/sensory disability, 95% reported stress and worry as one of their
25. 25
symptoms, 89% reported fatigue or lack of energy, and 89% reported poor sleep. Of
carers reporting that they cared for family and children, all of them reported feeling
fatigue or lack of energy, stress and worry, and poor sleep.
Of carers reporting that their main responsibilities included personal care, about 88%
reported poor sleep as a symptom, and 88% reported stress and worry. Of carers that
included providing physical assistance as one of their main responsibilities, 88% reported
feeling stress and worry, 87% reported fatigue or lack of energy, and 85%reported poor
sleep. Of carers indicating that providing emotional support was one of their main
responsibilities, 90% reported feeling stress and worry, 88% included fatigue or lack of
energy, and 86% reported poor sleep. Of carers reporting other as a main
responsibility, all of them reported fatigue or lack of energy as a symptom. Of carers
that listed household tasks as one of their main responsibilities, 90% reported fatigue or
lack of energy as a symptom, and 90% reported stress and worry.
Of carers that reported spending less than 20 hours caring a week, all of them reported
fatigue or lack of energy as a symptom they have experienced. Of those who reported
caring 20-50 hours, 93% reported having poor sleep. Of those carers who reported
caring for 50-100 hours, all of them reported stress and worry as a symptom, and 93%
reported poor sleep. Of carers that responded caring for more than 100 hours, 90%
reported having stress and worry.
26. 26
Table 5: Cross Tabulation--Time Commitments & Mental Health Symptoms
5. How much time do you spend caring each week?
Less than
20 hours
20-50
hours
50-100
hours
more than
100 hours
Total
7. What
mental
health
symptoms, if
any, have you
experienced?
none
0 0 0 0 0
0 0 0 0 0
low mood
5 10 12 34 61
62.5 66.67 80 72.34 71.76
fatigue or lack of
energy
8 12 13 41 74
100 80 86.67 87.23 87.06
lack of
enjoyment in life
4 7 7 30 48
50 46.67 46.67 63.83 56.47
stress and worry
6 13 15 42 76
75 86.67 100 89.36 89.41
frustration and
anger
5 9 12 36 62
62.5 60 80 76.6 72.94
poor sleep
4 14 14 41 73
50 93.33 93.33 87.23 85.88
restlessness
1 7 8 24 40
12.5 46.67 53.33 51.06 47.06
other(please
specify)
0 4 2 4 10
0 26.67 13.33 8.51 11.76
Total
8 15 15 47 85
100 100 100 100 100
27. 27
Figure 10: time commitment and mental health symptoms
Of carers that reported suffering from low mood, 59% marked the services as extremely
helpful and about 30% marked them as quite helpful. Of carers that reported suffering from
fatigue or lack of energy, 61% found the services extremely helpful and 28% found them
quite helpful. Of carers that reported suffering from lack of enjoyment in life, 54% marked
the services as extremely helpful, and 33% marked them as quite helpful. Of carers that
reported suffering from stress and worry, 64% marked the services as extremely helpful,
and 26% marked them as quite helpful. Of carers that reported frustration and anger, 65%
reported the services as extremely helpful. Of carers that reported poor sleep, 59% marked
the services as extremely helpful. Of carers who reported feeling restless, 53% reported
that the services with extremely helpful. The two carers that reported the services as
slightly helpful were carers who reported that they suffered from all the mental health
symptoms listed.
Stress relief and relaxation were the two most reported health needs that our services help
carers meet across all the mental health symptoms that carers reported as feeling.
The one carer whohad ratedthe servicesprovidedbythe centre asaverage reportedthatthey
sufferedfromall the mental healthsymptomslistedinthe survey. Foreachmental healthsymptom
categorylisted,over85%of the carers that reportedhavingeachsymptomratedthe servicesof the
centre as excellent.
0
20
40
60
80
100
120
0 1 2 3 4 5
percentofpeoplewhoexperiencethesymptom
Hours of care provided per week
low mood
fatigue or lack of energy
lack of enjoyment in life
stress and worry
frustration and anger
poor sleep
restlessness
28. 21%
13%
2%
8%
65%
42%
27% 27%
22%
27%
0%
10%
20%
30%
40%
50%
60%
70%
home help respite peer
support
groups
counseling financial
support
none
Additional Services
additional support received additional services desired
Additional Support
77.78% of mencomparedto only 38.16% of womenwantedrespite care. Currently,those currently
receivingthissupportsit
at 22.22% formenand
11.84% for women. One
thirdof men wanted
counsellingwhere one
ninthcurrentlyreceiveit.
26.32% of women
wantedcounselling
although28.95% of
womenare currently
receivingthismodality.
The biggestdiscrepancy
betweenreceivedand
desiredserviceswasin
‘peersupport
groups’where only
2% currentlyenjoy
thissupportand 27%
of ourcohort would
welcome it.
The more hours
invested in caring
for someone, the
less likely the carer
is to receive
support. Home
help services are
there for those
caring for less than
20 hours per week,
perhaps explain why they are required to spend so few hours in care. Basedon the comments
such as “I have no time tothinkaboutthis” and“If I leave there isnobodythere,”itcanbe deduced
that those whoprovide intensive care maybe unable todiverttime orattentionawayfromcaring
and therefore are notreceivinganyservices.
Other Comments
Wouldlike supportaftercaree passesaway
More information
I wouldn'tsendhimtoone of those homes.
I have a full time job.I’ma busdriver.I don'tthinkaboutthisstuff.
Have no time to thinkaboutthis
theyare fine the waytheyare (fromcarer for herhusbandwhohas early
dementia)
if I leave there isnobodythere;triedcounsellingdidn't help;wouldliketo
leave the house
Figure 11: Additional Services Received& Desired
29. 29
Table 6: Time Commitments & Other Services Received
5. How much time do you spend caring each week?
Less than
20 hours
20-50
hours
50-100
hours
more than
100 hours
Total
11. What other
services are you
receiving, if
any?
none
4 11 10 30 55
50 73.33 66.67 63.83 64.71
counselling
1 2 1 3 7
12.5 13.33 6.67 6.38 8.24
respite care
0 0 1 10 11
0 0 6.67 21.28 12.94
peer support
groups
0 0 1 1 2
0 0 6.67 2.13 2.35
other
0 2 0 3 5
0 13.33 0 6.38 5.88
home help
3 3 4 8 18
37.5 20 26.67 17.02 21.18
Total
8 15 15 47 85
100 100 100 100 100
30. Motivation for Services
One third of men felt they needed help to ‘cope’ compared to only 10.53% of women. Half
of our male clients were referred by a social worker and none were referred by a GP. Only
7.89% of women were referred by a GP but 71.05% of women were referred from a social
worker.
A vast majority (82%) of those who sought treatment because they needed help with
coping provide care for more than 100 hours a week. The more hours of care carers deliver,
the more likely carers sought treatment because they needed relaxation. Of those who
provide more than 100 hours a week, 40% sought treatment because they wanted
relaxation. Of those who provide care for less than 20 hours, 12% sought treatment because
they wanted relaxation. The same holds true for those who sought treatment because they
needed help with coping. No one who provides care for less than 20 hours a week sought
treatment because they couldn’t cope, compared to 19% of those who care for more than
100 hours a week, 7% of those who care for 50-100 hours a week and 7% of those who care
for 20-50 hours a week. We see the opposite trend for those who were referred by their
GPs. 25% of those who care for less than 20 hours were referred by their GPs but only % of
those who care for more than 100 hours were referred by their GPs
Those who were referred by their GPs are least likely to have experienced all of the mental
health symptoms. Those who were motivated by time for self are more likely to have
experienced low mood (88%) and frustration/anger (88%) than those motivated by other
reasons. Those who needed help for coping are more likely to have experienced lack of
enjoyment in life (64%) and restlessness (64%) (two of the less frequently experienced
symptoms) than those motivated by other causes. Those who needed relaxation are more
likely to have experienced poor sleep compared to those motivated by other causes.
Those who needed time or self (75%) are twice more likely not to receive any additional
support than those who were referred by their GPs. Those who needed help for coping are
the most likely to receive counselling those motivated by other causes. Those who were
referred by their GPs (17%) are the most likely to have received respite, more than twice
more likely than those who needed time for self (6%). No one who needed help for coping
received home help, compared to 33% of those who were referred by their GPs.
69%
35%
13%
19%
35%
0%
10%
20%
30%
40%
50%
60%
70%
80%
referred by
social worker
referred by gp needed help
for coping
time for self relaxation
Motivation for service
Figure 12: Motivation for Service
31. Usefulness of Services
62.35% of clientsfeltthe service was‘extremely
helpful’tothem,withonly2.63% reportingno
impactto theirhealthand wellbeingasaresultof
the therapies. Seekingamore nuanced
understandingof how the serviceswere helpful,
clientswere askedtoquantifythe assistance
provided. 91% reportedfeelingrelaxedaftereach
sessionwith80% reportinglongertermstressrelief
fromtheircaring duties. Forone quarterof clientsa
reductioninpainandan improvedqualityof life
meanttheyratedthe servicesas‘extremely
helpful’. Furthermore,85% of clientsrated
the service as‘excellent’and69% would
contribute to the provisionof theirtherapies
infuture. 7% notedthat theycouldnot
affordevena£5 contributionwhenasked
whytheywere ‘notat all likely’ tocontribute
to theirservices.
More women(64%) ratedthe servicesas
“extremelyhelpful”thanmen(44%).Menare
more likelytorate the servicesasquite or
moderatelyhelpful thanwomen.Two
womenratedthe servicesas“slightly
helpful”andtwowomenratedthe
servicesas“not at all helpful.” One of
those fourclientswasdissatisfiedwith
service because of administrative
complications(Seethe lastcomment
intable on the left).Three of the four
clientssufferedfromall of the mental
healthsymptoms,care formore than
100 hoursa weekandare not
receivinganyotherservices.All of
those whosoughtout the therapiesto
helpthem‘cope’ withdailytasks
ratedthe service asexcellent.
Other Comments Frequency
betterable tocope, but still alot of pain and
stress
5
Thingshave gone downhill;stresslevel
increasedtremendously
3
(relief of symptoms)justforawhile 9
canceledbecause of sexual assaultandtoo
much goingon
1
circumstanceschange daily,aninjectionof
calm at the time,not eradicate the causesof
stress,helpme cope at that time
1
The fewfirstsessionswere good, butthe
lastfewsessionswere movedabout. huge
breaksbetweenfirstandlastsessions,Had
argumentabouttiming(Ineededtogoin
the day) , uncertain when Iwouldhave last
sessions,more stress,nothelpful,
1 (fromthe
responder
whorated
qualityof
service as
“poor” and
“not at all
helpful”)
Figure 14: Usefulness of Services
Figure 13: Relief of Symptoms
32. 32
If we compare the responsesof carerswiththe responsesof general clients(datawere collectedina
surveyin2014), we can see that carers (91%) are more likelytofindourservice tobe relaxingthan
general clients(81%).More carers(48%) felthappieraftertherapythangeneral clients(34%).Carers
(25%) are lesslikelytoexperience improvedqualityof life thangeneral clients(35%) The comments
above can explainthis. Nine carersreportedthattherapiesonlyhelpedforawhile;therapiesdidnot
resolve the cause of theirmental healthproblemssuchasintense caringresponsibilitiesand
therefore didnotimprove theirqualityof lifeinthe longterm.
Women are more likely to meet all of the health needs than men. 100% of those who
provide care for 50-100 hours experienced relaxation. Those who care for more than 100
hours a week are least likely to experience improved quality of life and less pain compared
to those who care for fewer hours.
Those who experience lack of enjoyment in life and frustration (two of the less common
symptoms) are more likely to have experienced improved quality of life, sense of wellbeing
and less pain (three of the less common effects) after therapy compared to those suffering
from other symptoms. Those who experienced improved quality of life are more likely to
have experienced low mood, lack of enjoyment in life, frustration, poor sleep and
restlessness than those who met other health needs. Those who felt happier are most likely
to have experienced fatigue than those who had other health needs met. Those who felt
less pain are most likely to have experienced stress than those who had other health needs
met.
81 78
50
35 34 33
91
80
51
25
48
26
0
20
40
60
80
100
Relaxation Stress Relief Sense of
Wellbeing
Improved
Quality of Life
Happier Less Pain
Health Needs Met Through CHWB
Services
All Clients Carers
33. 33
Table 7: Cross Tabulation--Mental Health Symptoms & and Relief of Symptoms
7. What mental health symptoms, if any, have you experienced?
none
low
moo
d
fatig
ue
lack
of
enjo
yme
nt in
life
stres
s
frust
ratio
n
poor
sleep
restl
essn
ess
othe
r
Total
10.Which
of the
following
health
need(s)
do our
services
and
therapies
help you
meet?
none
0 1 2 1 1 1 2 1 0 2
0 1.64 2.7 2.08 1.32 1.61 2.74 2.5 0 2.35
stress
relief
0 48 58 39 63 51 59 33 8 68
0
78.6
9
78.3
8
81.2
5
82.8
9
82.2
6
80.8
2 82.5 80 80
relaxatio
n
0 55 66 42 71 58 67 38 9 77
0
90.1
6
89.1
9 87.5
93.4
2
93.5
5
91.7
8 95 90
90.5
9
improve
d quality
of life
0 19 18 16 19 20 20 11 4 21
0
31.1
5
24.3
2
33.3
3 25
32.2
6 27.4 27.5 40
24.7
1
sense of
wellbein
g
0 35 37 28 40 37 35 21 5 43
0
57.3
8 50
58.3
3
52.6
3
59.6
8
47.9
5 52.5 50
50.5
9
happier
0 32 37 25 38 32 36 20 3 41
0
52.4
6 50
52.0
8 50
51.6
1
49.3
2 50 30
48.2
4
less pain
0 16 18 14 21 20 20 11 3 22
0
26.2
3
24.3
2
29.1
7
27.6
3
32.2
6 27.4 27.5 30
25.8
8
other
(please
specify)
0 12 16 11 14 13 15 10 3 16
0
19.6
7
21.6
2
22.9
2
18.4
2
20.9
7
20.5
5 25 30
18.8
2
Total
0 61 74 48 76 62 73 40 10 85
100 100 100 100 100 100 100 100 100 100
Although27.12% of those referredbyasocial workerenjoyedpainrelief,the highestoutcome was
‘relaxation’. Interestingly,only 90%of those whosoughtrelaxationfelttheyachieveditintherapy,
although93% of this groupreportedstressrelief.100% of those whosoughtrelaxationorwere
referredbytheirGPsexperiencedrelaxation.27% of those whowere referredbyasocial worker
experiencedimprovedqualityof life comparedto7% of those whosoughtrelaxation. 27% of those
whowere referredbya social workerfeltlesspaincomparedto13% of those whosoughtrelaxation.
No one whowere referredbyasocial workerexperiencedsenseof wellbeingcomparedto63% of
those whosoughttime forself.67% of those whowere referredbytheirGPfelthappiercompared
to 27% of those whoneededhelpforcoping.
34. 34
Table 8: Motivation for Services and Helpfulness of Services
8. Why did you seek treatment at the Centre?
referred
by social
worker
referred
by GP
needed
help
for
coping
time
for
self
other relaxation Total
9. Were
the
services
and
treatments
you
received at
the Centre
helpful in
addressing
your m...
extremely
helpful
37 2 8 11 6 19 53
62.71 33.33 72.73 68.75 75 63.33 62.35
quite
helpful
16 4 3 3 2 9 24
27.12 66.67 27.27 18.75 25 30 28.24
moderately
helpful
2 0 0 2 0 2 4
3.39 0 0 12.5 0 6.67 4.71
slightly
helpful
2 0 0 0 0 0 2
3.39 0 0 0 0 0 2.35
not at all
helpful
2 0 0 0 0 0 2
3.39 0 0 0 0 0 2.35
Total
59 6 11 16 8 30 85
100 100 100 100 100 100 100
36. Recommendations
Future research shouldaskthe followingquestions;
1. Do you care alone?
2. Does your caring responsibilities prevent you accessing health services for yourself?
3. Do you exercise less due to your caring responsibilities?
4. How has caring impacted your ability to work?
5. How has caring impacted your personal relationships, social life or leisure time?
6. Do you have sufficient access to transportation, medical professionals, information,
etc.?
Althoughamajorityof clientsreportedthattheyfindtherapiesrelaxingandstressrelieving,onlya
quarterof respondentsreportedthattherapiesimprovedtheirqualityof lifeinthe longterm.
Clientsreportedthatstress,fatigueandothermental healthsymptomstendtoreturnafter
therapiesstopandtheircaringresponsibilitiesresumeorintensify. The Centre shouldmake aneffort
to lookafterclients’mental wellbeinginthe longterm. The Centre can(1) recommendmore
sessionstocarerswhodisplaymore seriousmental healthsymptoms;(2) introduce andrecommend
othersupportservices suchas respite,home helpandcounsellingtoclients,especiallythose who
have intense caringduties.
The researchhas shownthat a vast majorityof carersare willingtopay£5 persession.However,
some are unwillingtopaydue to financial constraints.The Centre canaskcarers for £5 of voluntary
donationspersession.
Duringthe survey,one respondentreportedthatschedulingcomplicationsmarredherexperience as
a customer.Several respondentsreportedthattheyhadwantedtoreceive more sessionsbutnever
heardback fromthe Centre.The Centre shouldminimize administrative confusionormistake in
orderto maximize customersatisfaction.
38. Bibliography
Ackroyd,S.& Hughes,J.,1981. Data Collection in Context, London:LongmanPublishing.
Age UK; Carers Trust; CarersUK; IndependentAge;MacmillanCancerSupport;Marie Curie Cancer
Care; MS SocietyandParkinson’sUK,2013. In Sicknessand in Health, London:CarersUK.
Baldwin,R.,2002. Depressive Disorders.In:R.Jacoby& C. Oppenheimer,eds. Psychiatry in the
Elderly. Oxford:OxfordUniversityPress,pp.627-676.
CarersUK; Universityof Leeds,2011. Carers2011: Calculating the valueof carers’ support, London:
CarersUK.
CarersUK, 2014. State of Caring 2014, London:CarersUk.
CaresUK, 2001. It Could Be You – A report on the chancesof becoming a carer, London:Carers UK.
Furnham,A.,1986. Response bias,social desirabilityanddissimulation.. Personality and individual
differences, pp.385-400.
Goldie,I.& McCulloch,A.,2010. Public MentalHealth Today. Brighton:PavilionPublishingLtd.
Halliwell,E.,Main,L.& Richardson,C.,2007. The FundamentalFacts:TheLatestFacts and Figureson
MentalHealth, London:Mental HealthFoundation.
Knauper,B.& Wittechen,H.,1994. Diagnosingmajordepressioninthe elderly –evidence for
response biasinstandardizeddiagnosticinterviews.. Journalof PsychiatricResearch , pp.28. 147-
164.
National Statistics,2003. Better Or Worse:A Follow-Up Study Of TheMentalHealth OfAdultsin Great
Britain, London:National Statistics.
NHS InformationCentre,2010. Survey of Carersin Households2009/10, London:The Healthand
Social Care InformationCentre.
NHS,2003. NationalInstituteforHealth and Clinical Excellence, Depression,NICEGuideline, Second
Consultation, London:NHS.
Singleton,R.etal.,2001. PsychiatricMorbidity Among Adults2000. London:The StationeryOffice.
Walker,H.,Scarlett,M. & Williams,B.,2014. Health Survey Northern Ireland:FirstResults 2013/14,
Belfast:Departmentof Health,Social ServicesandPublicSafety.
Watson,D., 1992. CorrectingforAcquiescentResponseBiasinthe Absence of aBalancedScale An
ApplicationtoClassConsciousnessAugust1992. SociologicalMethodsResearch, pp.vol.21 no.1 52-
88.
39. Appendix
Appendix I Raw Data from Survey
1. What is your
gender?
3. What category of disability does
the person you are caring for
belong to?
Female Male Total
olderperson
34 5 39
44.74 55.56 45.88
learningdisability
10 0 10
13.16 0 11.76
physical/sensorydisability
15 3 18
19.74 33.33 21.18
mental health problem
12 1 13
15.79 11.11 15.29
familyand children
5 0 5
6.58 0 5.88
Total
76 9 85
100 100 100
4. What are your main
responsibilities?
personal care (e.g.washing,
dressing)
58 9 67
76.32 100 78.82
physical assistance (e.g.helpto
walk or climbstairs)
59 8 67
77.63 88.89 78.82
emotional support (e.g.listening,
offeringadvice and friendship)
66 7 73
86.84 77.78 85.88
other (please specify)
4 0 4
5.26 0 4.71
householdtasks (e.g.cooking,
shopping)
67 6 73
88.16 66.67 85.88
Total
76 9 85
100 100 100
5. How much time do you spend
caring each week?
Less than 20 hours
7 1 8
9.21 11.11 9.41
20-50 hours
14 1 15
18.42 11.11 17.65
50-100 hours
13 2 15
17.11 22.22 17.65
more than 100 hours
42 5 47
55.26 55.56 55.29
40. 40
Total
76 9 85
100 100 100
6. what is(are) your biggest
challenge(s) as a carer?
emotional challenges(e.g.social
isolation, stress,worry)
73 8 81
96.05 88.89 95.29
physical challenges(e.g.back pain,
tiredness)
37 5 42
48.68 55.56 49.41
financial issues(e.g.work care
balance)
20 2 22
26.32 22.22 25.88
other (please specify)
3 0 3
3.95 0 3.53
Total
76 9 85
100 100 100
7. What mental health
symptoms, if any, have you
experienced?
none
0 0 0
0 0 0
low mood
56 5 61
73.68 55.56 71.76
fatigue or lack of energy
67 7 74
88.16 77.78 87.06
lack of enjoymentinlife
44 4 48
57.89 44.44 56.47
stress and worry
71 5 76
93.42 55.56 89.41
frustration and anger
56 6 62
73.68 66.67 72.94
poor sleep
65 8 73
85.53 88.89 85.88
restlessness
36 4 40
47.37 44.44 47.06
other(please specify)
9 1 10
11.84 11.11 11.76
Total
76 9 85
100 100 100
8. Why did you seek treatment
at the Centre?
referredby social worker
54 5 59
71.05 55.56 69.41
referredby GP
6 0 6
7.89 0 7.06
neededhelpforcoping
8 3 11
10.53 33.33 12.94
time for self
14 2 16
18.42 22.22 18.82
other (please specify) 7 1 8
41. 41
9.21 11.11 9.41
relaxation
27 3 30
35.53 33.33 35.29
Total
76 9 85
100 100 100
9. Were the services and
treatments you received at the
Centre helpful in addressing your
mental health needs?
extremelyhelpful
49 4 53
64.47 44.44 62.35
quite helpful
20 4 24
26.32 44.44 28.24
moderatelyhelpful
3 1 4
3.95 11.11 4.71
slightlyhelpful
2 0 2
2.63 0 2.35
not at all helpful
2 0 2
2.63 0 2.35
Total
76 9 85
100 100 100
10. Which of the following
health need(s) do our services and
therapies help you meet, if a...
none
1 1 2
1.32 11.11 2.35
stress relief
63 5 68
82.89 55.56 80
relaxation
70 7 77
92.11 77.78 90.59
improvedquality oflife
19 2 21
25 22.22 24.71
sense of wellbeing
40 3 43
52.63 33.33 50.59
happier
39 2 41
51.32 22.22 48.24
lesspain
20 2 22
26.32 22.22 25.88
other (please specify)
14 2 16
18.42 22.22 18.82
Total
76 9 85
100 100 100
11. What other services are you
receiving, if any?
none
50 5 55
65.79 55.56 64.71
counselling
6 1 7
7.89 11.11 8.24
respite care
9 2 11
11.84 22.22 12.94
peersupport groups
1 1 2
1.32 11.11 2.35
42. 42
other (please specify)
4 1 5
5.26 11.11 5.88
home help
16 2 18
21.05 22.22 21.18
Total
76 9 85
100 100 100
12. what other servicescould be
useful for you?
none
22 1 23
28.95 11.11 27.06
counselling
20 3 23
26.32 33.33 27.06
respite care
29 7 36
38.16 77.78 42.35
peer support groups
21 2 23
27.63 22.22 27.06
financial support
17 2 19
22.37 22.22 22.35
other (please specify)
9 2 11
11.84 22.22 12.94
Total
76 9 85
100 100 100
13. How would you rate the
services and therapies you have
received at the Centre for Healt...
excellent
67 6 73
88.16 66.67 85.88
good
7 3 10
9.21 33.33 11.76
average
1 0 1
1.32 0 1.18
poor
1 0 1
1.32 0 1.18
Total
76 9 85
100 100 100
14. Would you have sought
treatment at the Centre if you had
to pay £5 for each session?
Extremelylikely
52 7 59
68.42 77.78 69.41
Quite likely
17 0 17
22.37 0 20
Not at all likely
5 1 6
6.58 11.11 7.06
moderatelylikely
2 1 3
2.63 11.11 3.53
slightlylikely
0 0 0
0 0 0
Total
76 9 85
100 100 100