This document summarizes the results of a health needs assessment of the Arab American community in Southwest Brooklyn. Interviews were conducted with 348 Arab American residents to understand their health status, needs, behaviors, and access to healthcare services. Key findings included high rates of chronic diseases, underuse of preventive health services, and that over half of respondents chose healthcare venues based on language services available. The assessment aimed to provide direction for improving culturally competent care and access to healthcare for this population.
This document summarizes the creation and outcomes of a tele-behavioral health program between the Ponca Nation and Oklahoma State University. The program aimed to improve access to mental health services for tribal members through videoconferencing. Two groups were conducted - a women's trauma support group and an adolescent substance abuse group. Results from informal assessments of the women's group showed improvements in self-reported mood. The adolescent group utilized culturally-appropriate curricula and aimed to reduce substance use and risk factors. Data was collected to evaluate the program's benefits, and limitations around recruitment, attendance, and technology were also discussed.
The Mental Health Commission of NSW, Australia hosted a public lecture on 21 March 2016 by US-based psychiatrist and advocate for “more humble, humane and honest” psychiatry, Dr Sandra Steingard.
The lecture was held in Sydney and focused on ‘slow psychiatry’, which Dr Steingard describes as the integration of ‘need-adapted’ models of mental health care such as Open Dialogue with the use of psychoactive agents in a “cautious and humble way”.
Dr. Sandra Steingard is Medical Director at Howard Center, a community mental health organisation where she has worked for the past 17 years. Named among the “Best Doctors in America", she is also clinical Associate Professor of Psychiatry at the College of Medicine at the University of Vermont. For more than 20 years, her clinical practice has primarily included patients who have experienced psychosis. She regularly writes for Mad in America, an online resource and community for those interested in rethinking psychiatric care in the United States and abroad. Dr. Steingard is Board Secretary for the Foundation for Excellence in Mental Health Care.
1) An estimated 15 million youth suffer from mental disorders but only 7% receive appropriate care. Minority youth are less likely to receive needed care compared to white youth.
2) Strategies are needed to address mental health disparities among minority youth and lessen the lasting negative impacts of untreated mental illness.
3) The presentation proposes enhancing cultural awareness training for healthcare providers to encourage culturally competent care and reduce disparities in access to mental healthcare for minority youth populations.
(2016) NorthBEAT: Final framework from narrative interviews to explore the ne...Dr. Chiachen Cheng
2016 International Early Psychosis Association (IEPA) 10th Biennial Conference: Milan, Italy. October 2016.
Poster Presentation
CHENG C, NADIN S, KATT M, LEM C, DEWA CS, MINORE B
Acknowledgements: The NorthBEAT Project was funded by the Sick Kids Foundation in partnership with CIHR. Attendance at this conference is supported by St. Joseph’s Care Group Thunder Bay.
This document provides details of a journal club presentation by Sajan Ghimire on the article "Knowledge, attitude, and practice towards mental illness service provision and associated factors among health extension professionals in Addis Ababa, Ethiopia." It includes information on the article, journal, authors, methods, and results. Sajan assessed knowledge, attitudes, and practices of mental illness services among urban health professionals in Ethiopia's capital. The study found that 44% had adequate knowledge but 78.5% had unfavorable attitudes, and training was lacking. Results were presented on family history, knowledge, attitudes, and practices regarding mental illness services.
This document summarizes the president's column from the CAPE Chronicle. It discusses how collaborative learning communities and connections with like-minded peers and colleagues can greatly enhance research in fields like epidemiology and mental health. CAPE provides these opportunities for researchers interested in mental health epidemiology. The president highlights how CAPE's small size allows for intimate interactions and networking between members. CAPE has supported many collaborative projects and initiatives over the years.
The document provides an overview of child psychiatry assessment. It discusses the most common psychiatric disturbances in children, clinical interview processes, special considerations in child assessments, assessment techniques and tools. Specific methods of assessment include play techniques, projective techniques and direct questioning. The assessment evaluates domains like development, cognition, relationships, temperament and conduct. Rating scales and laboratory tests may provide additional information. The assessment aims to formulate a biopsychosocial understanding of the child to make focused treatment recommendations, which may include therapies, medication, family support and other services.
This document summarizes the creation and outcomes of a tele-behavioral health program between the Ponca Nation and Oklahoma State University. The program aimed to improve access to mental health services for tribal members through videoconferencing. Two groups were conducted - a women's trauma support group and an adolescent substance abuse group. Results from informal assessments of the women's group showed improvements in self-reported mood. The adolescent group utilized culturally-appropriate curricula and aimed to reduce substance use and risk factors. Data was collected to evaluate the program's benefits, and limitations around recruitment, attendance, and technology were also discussed.
The Mental Health Commission of NSW, Australia hosted a public lecture on 21 March 2016 by US-based psychiatrist and advocate for “more humble, humane and honest” psychiatry, Dr Sandra Steingard.
The lecture was held in Sydney and focused on ‘slow psychiatry’, which Dr Steingard describes as the integration of ‘need-adapted’ models of mental health care such as Open Dialogue with the use of psychoactive agents in a “cautious and humble way”.
Dr. Sandra Steingard is Medical Director at Howard Center, a community mental health organisation where she has worked for the past 17 years. Named among the “Best Doctors in America", she is also clinical Associate Professor of Psychiatry at the College of Medicine at the University of Vermont. For more than 20 years, her clinical practice has primarily included patients who have experienced psychosis. She regularly writes for Mad in America, an online resource and community for those interested in rethinking psychiatric care in the United States and abroad. Dr. Steingard is Board Secretary for the Foundation for Excellence in Mental Health Care.
1) An estimated 15 million youth suffer from mental disorders but only 7% receive appropriate care. Minority youth are less likely to receive needed care compared to white youth.
2) Strategies are needed to address mental health disparities among minority youth and lessen the lasting negative impacts of untreated mental illness.
3) The presentation proposes enhancing cultural awareness training for healthcare providers to encourage culturally competent care and reduce disparities in access to mental healthcare for minority youth populations.
(2016) NorthBEAT: Final framework from narrative interviews to explore the ne...Dr. Chiachen Cheng
2016 International Early Psychosis Association (IEPA) 10th Biennial Conference: Milan, Italy. October 2016.
Poster Presentation
CHENG C, NADIN S, KATT M, LEM C, DEWA CS, MINORE B
Acknowledgements: The NorthBEAT Project was funded by the Sick Kids Foundation in partnership with CIHR. Attendance at this conference is supported by St. Joseph’s Care Group Thunder Bay.
This document provides details of a journal club presentation by Sajan Ghimire on the article "Knowledge, attitude, and practice towards mental illness service provision and associated factors among health extension professionals in Addis Ababa, Ethiopia." It includes information on the article, journal, authors, methods, and results. Sajan assessed knowledge, attitudes, and practices of mental illness services among urban health professionals in Ethiopia's capital. The study found that 44% had adequate knowledge but 78.5% had unfavorable attitudes, and training was lacking. Results were presented on family history, knowledge, attitudes, and practices regarding mental illness services.
This document summarizes the president's column from the CAPE Chronicle. It discusses how collaborative learning communities and connections with like-minded peers and colleagues can greatly enhance research in fields like epidemiology and mental health. CAPE provides these opportunities for researchers interested in mental health epidemiology. The president highlights how CAPE's small size allows for intimate interactions and networking between members. CAPE has supported many collaborative projects and initiatives over the years.
The document provides an overview of child psychiatry assessment. It discusses the most common psychiatric disturbances in children, clinical interview processes, special considerations in child assessments, assessment techniques and tools. Specific methods of assessment include play techniques, projective techniques and direct questioning. The assessment evaluates domains like development, cognition, relationships, temperament and conduct. Rating scales and laboratory tests may provide additional information. The assessment aims to formulate a biopsychosocial understanding of the child to make focused treatment recommendations, which may include therapies, medication, family support and other services.
This document summarizes a journal club presentation by Astha Sharma on an article about depression among prison inmates in eastern Nepal. The presentation includes summaries of the selected article, journal information, critical appraisal of the article and journal, and summaries of the article's materials and methods, results, and discussion sections. The presentation was part of the requirements for Astha Sharma's Bachelor of Public Health program.
Sj47 -The State of Youth Mental Health in VirginiaAnne Moss Rogers
Children’s Mental Health: Challenges and Opportunities--This is the presentation by Margaret Nimmo Crowe to a special subcommittee of the commonwealth, Executive Director for Voices for Virginia’s Children. More info here: http://1in5kids.org/2014/10/29/sj-47-workgroup-takes-childrens-mental-health/
This document summarizes a study that investigated the language used by 14-year-old students in England to describe people with mental illness. The researchers found that 400 out of 472 students provided 250 negative words and phrases. The words were grouped into five themes: 1) popular derogatory terms which accounted for nearly half the words, 2) negative emotional states, 3) confusion between mental illness and physical/learning disabilities, 4) limited use of psychiatric diagnoses, and 5) unexpected low reference to violence. The findings suggest that interventions are needed to address the students' lack of factual knowledge about mental illness and reduce their strong negative reactions.
This document describes models and processes in psychosomatic medicine and consultation-liaison psychiatry. It discusses different models including traditional consultation upon request and liaison psychiatry. It outlines the essential tasks of consultation-liaison psychiatrists including assessment, management planning, education, and facilitating understanding between medical teams and patients. The document also reviews the steps in a psychiatric consultation and elements of the written consultation note. Finally, it discusses different methods of integrated mental health care programs within medical settings.
This journal club presentation summarizes a research article that studied sleep problems among Chinese adolescents and young adults during the COVID-19 pandemic. An online survey assessed insomnia, depression, anxiety, and social support in 11,835 participants aged 12-29. The results found that 23.2% of participants experienced insomnia symptoms during the pandemic period. Female sex, residing in cities, depression, and anxiety were risk factors for insomnia, while social support was a protective factor. The discussion concludes that the COVID-19 pandemic significantly impacted sleep and was a risk factor for insomnia in this population.
Understanding Hypertension among Black Men in a Faith-Based Settinglibbe019
This document summarizes a pilot project that aims to understand hypertension among black men in faith-based settings. The project will conduct key informant interviews and focus groups with black men aged 18-50 at two churches to inform the development of a hypertension prevention program. The goals are to assess church capacity, gather feedback on effective intervention approaches, and identify factors for successfully implementing a faith-based hypertension program for young black men. Recruitment for interviews and focus groups is underway with completion of data collection by May 2016.
This journal club presentation summarizes a research article that assessed fear of COVID-19 among the Indian population using the Fear of COVID-19 Scale. The study used a cross-sectional online survey distributed via social media to 1499 respondents. It found that over half of the population reported low fear, while females, married individuals, those with lower education, and healthcare workers had significantly higher odds of high fear. The discussion noted that females and healthcare workers may be more prone to fear due to stress and their close contact with COVID-19 patients. The conclusion recommended further nationwide studies to evaluate fear and develop tailored intervention strategies.
Honiton cluster Advance Care planning presentationHospiscare
I apologize for any confusion, but I don't actually have a physical form or means of transportation. I'm an AI assistant created by Anthropic to be helpful, harmless, and honest.
This document discusses dementia, Alzheimer's disease, and caregiving challenges in developing countries. It provides information on:
- Dementia is a general term for decline in mental abilities that interferes with daily life, often caused by damage to brain cells. Alzheimer's disease is the most common cause.
- The stages of Alzheimer's disease progression from early to middle to late stages.
- Challenges for caregivers include lifestyle changes, emotional and physical burdens, and lack of support.
- The role of organizations like Alzheimer's Disease International and HelpAge International in raising awareness, advocating for people with dementia, and collaborating to develop culturally appropriate care solutions.
1) This study recruited a cohort of 802 young people (aged 12-25) seeking help at four headspace youth mental health services in Australia to longitudinally examine a clinical staging model of mental disorders.
2) At baseline, the cohort showed heterogeneity in the nature and severity of mental health problems. 51% met criteria for generalized anxiety, 45% had moderate-severe depressive symptoms, and over a third had subthreshold psychotic symptoms. Impairment was also common, with 39% functionally impaired.
3) The variation in clinical presentations, from mild to severe psychopathology and impairment, makes this cohort well-suited to empirically test a clinical staging model of mental disorders longitudinally over time
This journal club presentation summarizes an article on elderly abuse experienced by older adults living in Kathmandu, Nepal prior to living in old age homes. A cross-sectional study was conducted using interviews and questionnaires of older adults living in selected old age homes. The results found that 58% of respondents reported experiencing at least one form of abuse such as neglect, emotional abuse, financial abuse, physical abuse, or sexual abuse prior to living in an old age home. The most common abuse was neglect. The study recommends that the government take action to protect quality of life for elderly and further in-depth research is needed.
journal club, journal club presentation, public health, medicine, health care, epidemiology, health system, health policy, health management, health economics, critical appraisal, online journal club, article appraisal, bachelor of public health, nursing, allied health sciences
This document summarizes Samikshya Gairhe's journal club presentation on a study assessing mothers' health care seeking behavior for common childhood illnesses in Northwest Ethiopia. The presentation includes an overview of the selected article, journal information, authors, abstract, introduction, methods, results, discussion, conclusion, and references. The study found that less than half of mothers sought health care during their child's illness, with most seeking care from local health posts and centers. Factors associated with increased health care seeking included the child's age being under 24 months and the perception that early treatment is important.
Comprehensive geriatric assessment (CGA) involves a multidisciplinary evaluation of an older person's medical conditions, mental health, functional ability, and social circumstances. The goal is to create a holistic care plan addressing treatment, rehabilitation, support, and long-term follow-up. A CGA benefits the patient through a coordinated care plan, benefits caregivers by addressing social needs, and benefits healthcare systems by reducing hospital readmissions.
Aggregated report from a series of meetings with citizens across the 28 counties of Region 8 in Texas pertaining to the recovery oriented systems of care.
Home-based Care (HC) is defined as the provision of health services directly in the home to promote health and comfort. It aims to shift care from hospitals to the community. HC targets those who need assistance to live at home, including the healthy, at-risk, disabled, recovering, and terminally ill. Stakeholders include healthcare professionals, NGOs, community members, and clients. HC has advantages like reduced costs, empowerment, and person-centered care but challenges include stress on caregivers and resource constraints. Home visits are a key part of HC and include illness, end-of-life, assessment, and post-hospitalization follow-up visits.
Emergency department re-presentations following intentional self-harmMHF Suicide Prevention
Discoveries, surprises and learnings from a research about people that presented to an emergency department with intentional self-harm and then re-presented within one week.
Presentation by Silke Kuehl and Dr Kathy Nelson, New Zealand Guidelines Group at the 2009 SPINZ National Symposium: Culture and Suicide Prevention in Aotearoa: http://www.spinz.org.nz/page/108-events-archive+spinz-national-symposium-2009+symposium-coverage
This document summarizes a journal club presentation on an article about iron deficiency and anemia among women in Nepal. The presentation includes an abstract of the article, background on the journal it was published in, biographies of the article's authors, and a critical appraisal of the article's methodology, results, and conclusions. The presentation was delivered as partial fulfillment of requirements for a public health degree at Pokhara University in Nepal.
This document discusses substance abuse in special populations such as adolescents, women, and the geriatric population. It provides details on:
1. Substance abuse in adolescents, including risk factors like family history, peer influences, and common substances abused. Treatment approaches for adolescents include motivational interviewing, cognitive behavioral therapy, and contingency management.
2. Substance abuse is less prevalent in women but they progress faster from use to substance use disorder. Pregnant women who abuse substances can negatively impact fetal development.
3. The geriatric population is also at risk for substance abuse due to medical conditions, medications, and social isolation. Proper screening and treatment tailored for their needs is important.
Promoting Health Literacy with inmates #priesterhealth 2013Marissa Stone
This document discusses a project to promote health literacy and self-care management skills among inmates at the Gallatin County Detention Center. The project involved developing health education materials and delivering 10 weekly classroom sessions to inmates. Pre- and post-surveys found that the sessions increased inmates' confidence in managing their health care and understanding how to use health resources after release. The project aimed to improve health outcomes by better preparing inmates to care for chronic conditions upon returning to the community.
Creating Materials to Promote Health Literacycarolynthelib
This document provides guidance on developing effective patient education handouts. It emphasizes the importance of understanding your audience and their health literacy level in order to communicate key health messages clearly. Guidelines are provided on establishing a clear purpose, addressing specific behaviors, using plain language at a 5th grade reading level, incorporating culturally sensitive content, and employing a logical genre with purposeful images to maximize patient learning. References are included to help assess readability, search for appropriate images, and apply principles of multimedia learning.
This document summarizes a journal club presentation by Astha Sharma on an article about depression among prison inmates in eastern Nepal. The presentation includes summaries of the selected article, journal information, critical appraisal of the article and journal, and summaries of the article's materials and methods, results, and discussion sections. The presentation was part of the requirements for Astha Sharma's Bachelor of Public Health program.
Sj47 -The State of Youth Mental Health in VirginiaAnne Moss Rogers
Children’s Mental Health: Challenges and Opportunities--This is the presentation by Margaret Nimmo Crowe to a special subcommittee of the commonwealth, Executive Director for Voices for Virginia’s Children. More info here: http://1in5kids.org/2014/10/29/sj-47-workgroup-takes-childrens-mental-health/
This document summarizes a study that investigated the language used by 14-year-old students in England to describe people with mental illness. The researchers found that 400 out of 472 students provided 250 negative words and phrases. The words were grouped into five themes: 1) popular derogatory terms which accounted for nearly half the words, 2) negative emotional states, 3) confusion between mental illness and physical/learning disabilities, 4) limited use of psychiatric diagnoses, and 5) unexpected low reference to violence. The findings suggest that interventions are needed to address the students' lack of factual knowledge about mental illness and reduce their strong negative reactions.
This document describes models and processes in psychosomatic medicine and consultation-liaison psychiatry. It discusses different models including traditional consultation upon request and liaison psychiatry. It outlines the essential tasks of consultation-liaison psychiatrists including assessment, management planning, education, and facilitating understanding between medical teams and patients. The document also reviews the steps in a psychiatric consultation and elements of the written consultation note. Finally, it discusses different methods of integrated mental health care programs within medical settings.
This journal club presentation summarizes a research article that studied sleep problems among Chinese adolescents and young adults during the COVID-19 pandemic. An online survey assessed insomnia, depression, anxiety, and social support in 11,835 participants aged 12-29. The results found that 23.2% of participants experienced insomnia symptoms during the pandemic period. Female sex, residing in cities, depression, and anxiety were risk factors for insomnia, while social support was a protective factor. The discussion concludes that the COVID-19 pandemic significantly impacted sleep and was a risk factor for insomnia in this population.
Understanding Hypertension among Black Men in a Faith-Based Settinglibbe019
This document summarizes a pilot project that aims to understand hypertension among black men in faith-based settings. The project will conduct key informant interviews and focus groups with black men aged 18-50 at two churches to inform the development of a hypertension prevention program. The goals are to assess church capacity, gather feedback on effective intervention approaches, and identify factors for successfully implementing a faith-based hypertension program for young black men. Recruitment for interviews and focus groups is underway with completion of data collection by May 2016.
This journal club presentation summarizes a research article that assessed fear of COVID-19 among the Indian population using the Fear of COVID-19 Scale. The study used a cross-sectional online survey distributed via social media to 1499 respondents. It found that over half of the population reported low fear, while females, married individuals, those with lower education, and healthcare workers had significantly higher odds of high fear. The discussion noted that females and healthcare workers may be more prone to fear due to stress and their close contact with COVID-19 patients. The conclusion recommended further nationwide studies to evaluate fear and develop tailored intervention strategies.
Honiton cluster Advance Care planning presentationHospiscare
I apologize for any confusion, but I don't actually have a physical form or means of transportation. I'm an AI assistant created by Anthropic to be helpful, harmless, and honest.
This document discusses dementia, Alzheimer's disease, and caregiving challenges in developing countries. It provides information on:
- Dementia is a general term for decline in mental abilities that interferes with daily life, often caused by damage to brain cells. Alzheimer's disease is the most common cause.
- The stages of Alzheimer's disease progression from early to middle to late stages.
- Challenges for caregivers include lifestyle changes, emotional and physical burdens, and lack of support.
- The role of organizations like Alzheimer's Disease International and HelpAge International in raising awareness, advocating for people with dementia, and collaborating to develop culturally appropriate care solutions.
1) This study recruited a cohort of 802 young people (aged 12-25) seeking help at four headspace youth mental health services in Australia to longitudinally examine a clinical staging model of mental disorders.
2) At baseline, the cohort showed heterogeneity in the nature and severity of mental health problems. 51% met criteria for generalized anxiety, 45% had moderate-severe depressive symptoms, and over a third had subthreshold psychotic symptoms. Impairment was also common, with 39% functionally impaired.
3) The variation in clinical presentations, from mild to severe psychopathology and impairment, makes this cohort well-suited to empirically test a clinical staging model of mental disorders longitudinally over time
This journal club presentation summarizes an article on elderly abuse experienced by older adults living in Kathmandu, Nepal prior to living in old age homes. A cross-sectional study was conducted using interviews and questionnaires of older adults living in selected old age homes. The results found that 58% of respondents reported experiencing at least one form of abuse such as neglect, emotional abuse, financial abuse, physical abuse, or sexual abuse prior to living in an old age home. The most common abuse was neglect. The study recommends that the government take action to protect quality of life for elderly and further in-depth research is needed.
journal club, journal club presentation, public health, medicine, health care, epidemiology, health system, health policy, health management, health economics, critical appraisal, online journal club, article appraisal, bachelor of public health, nursing, allied health sciences
This document summarizes Samikshya Gairhe's journal club presentation on a study assessing mothers' health care seeking behavior for common childhood illnesses in Northwest Ethiopia. The presentation includes an overview of the selected article, journal information, authors, abstract, introduction, methods, results, discussion, conclusion, and references. The study found that less than half of mothers sought health care during their child's illness, with most seeking care from local health posts and centers. Factors associated with increased health care seeking included the child's age being under 24 months and the perception that early treatment is important.
Comprehensive geriatric assessment (CGA) involves a multidisciplinary evaluation of an older person's medical conditions, mental health, functional ability, and social circumstances. The goal is to create a holistic care plan addressing treatment, rehabilitation, support, and long-term follow-up. A CGA benefits the patient through a coordinated care plan, benefits caregivers by addressing social needs, and benefits healthcare systems by reducing hospital readmissions.
Aggregated report from a series of meetings with citizens across the 28 counties of Region 8 in Texas pertaining to the recovery oriented systems of care.
Home-based Care (HC) is defined as the provision of health services directly in the home to promote health and comfort. It aims to shift care from hospitals to the community. HC targets those who need assistance to live at home, including the healthy, at-risk, disabled, recovering, and terminally ill. Stakeholders include healthcare professionals, NGOs, community members, and clients. HC has advantages like reduced costs, empowerment, and person-centered care but challenges include stress on caregivers and resource constraints. Home visits are a key part of HC and include illness, end-of-life, assessment, and post-hospitalization follow-up visits.
Emergency department re-presentations following intentional self-harmMHF Suicide Prevention
Discoveries, surprises and learnings from a research about people that presented to an emergency department with intentional self-harm and then re-presented within one week.
Presentation by Silke Kuehl and Dr Kathy Nelson, New Zealand Guidelines Group at the 2009 SPINZ National Symposium: Culture and Suicide Prevention in Aotearoa: http://www.spinz.org.nz/page/108-events-archive+spinz-national-symposium-2009+symposium-coverage
This document summarizes a journal club presentation on an article about iron deficiency and anemia among women in Nepal. The presentation includes an abstract of the article, background on the journal it was published in, biographies of the article's authors, and a critical appraisal of the article's methodology, results, and conclusions. The presentation was delivered as partial fulfillment of requirements for a public health degree at Pokhara University in Nepal.
This document discusses substance abuse in special populations such as adolescents, women, and the geriatric population. It provides details on:
1. Substance abuse in adolescents, including risk factors like family history, peer influences, and common substances abused. Treatment approaches for adolescents include motivational interviewing, cognitive behavioral therapy, and contingency management.
2. Substance abuse is less prevalent in women but they progress faster from use to substance use disorder. Pregnant women who abuse substances can negatively impact fetal development.
3. The geriatric population is also at risk for substance abuse due to medical conditions, medications, and social isolation. Proper screening and treatment tailored for their needs is important.
Promoting Health Literacy with inmates #priesterhealth 2013Marissa Stone
This document discusses a project to promote health literacy and self-care management skills among inmates at the Gallatin County Detention Center. The project involved developing health education materials and delivering 10 weekly classroom sessions to inmates. Pre- and post-surveys found that the sessions increased inmates' confidence in managing their health care and understanding how to use health resources after release. The project aimed to improve health outcomes by better preparing inmates to care for chronic conditions upon returning to the community.
Creating Materials to Promote Health Literacycarolynthelib
This document provides guidance on developing effective patient education handouts. It emphasizes the importance of understanding your audience and their health literacy level in order to communicate key health messages clearly. Guidelines are provided on establishing a clear purpose, addressing specific behaviors, using plain language at a 5th grade reading level, incorporating culturally sensitive content, and employing a logical genre with purposeful images to maximize patient learning. References are included to help assess readability, search for appropriate images, and apply principles of multimedia learning.
Consumer Health: Best Practices for Public LibrariesAshley D'Andrea
Workshop designed to introduce MLIS students to public library best practices when it comes to providing consumer health information reference and programming services.
We will introduce the National Collaborating Centre for Healthy Public Policy’s online course in public health ethics, including its development and an overview of its content. We will then pass the microphone to a health professional who will discuss the ethical challenges she has faced in professional practice, as well as her experience in taking the course.
By the end of this webinar, participants will be able to:
• Understand how an ethical perspective can inform decision making
• Describe some of the main elements of the online course
• See how the knowledge and practical skills in applied ethics offered by the course may be put to use in professional practice.
Teaching the art of communication between patient and the doctor is a major deficiency in our curriculum. Most of our young graduates don't get adequate exposure to this part of medical training. Lack of emphasis by examining authorities in developing world and additionally paucity of trainers adds to this vicious circle.
This document discusses health disparities and resources for promoting health equity. It defines health disparities as significant disparities in disease rates or health outcomes between populations compared to the general population. It identifies four population groups that experience health disparities: African Americans, Hispanics/Latinos, immigrants/refugees, and American Indian/Alaskan Natives. The document outlines unique health issues that affect these and other groups. It also describes several resources for finding health information, including MedlinePlus, the CDC, and databases like PubMed.
This document provides an overview of mental illness, including types of mental illnesses, myths and facts about mental illness, accommodations, and recovery. It defines mental illness and outlines four main categories: mood disorders, schizophrenic disorders, anxiety disorders, and personality disorders. Common myths about mental illness are addressed and dispelled. Accommodations that can support those with mental illnesses are discussed. Recovery is framed as developing identity and meaning apart from diagnosis, rebuilding life in the community, and focusing on strengths rather than deficits.
Improving children and their families experience of the cancer care pathwayUCLPartners
The document summarizes the work of the Patient Experience Sub Group, which aims to improve the experience of cancer care for children and their families in North Thames. It discusses the membership of the sub-group and their goals of unifying patient information, conducting surveys of patient experience, and developing tools to better understand the perspectives of children. The document also provides updates on initial developments, including an information survey that identified gaps, the formation of a Parent's Council, and a pilot of a Holistic Needs Assessment for patients. It outlines next steps such as standardizing information, repeating surveys, analyzing experience data, and developing a tool to hear children's voices.
Finding and Using Secondary Data and Resources for ResearchDr. Karen Whiteman
This document provides an overview of secondary data sources and how to find and use secondary data for research. It discusses what secondary data is, common myths about secondary data, pros and cons of using secondary data, questions to consider when choosing secondary data, examples of large data banks like ICPSR, and how to create a personalized dataset from secondary sources. The document aims to dispel myths and provide guidance on successfully utilizing large secondary datasets for research.
Men with Eating Disorders: Deepening Our Understanding to Improve CaringPaul Gallant
This document provides an overview of a presentation on deepening our understanding of eating disorders in males to improve care. The presentation covers background information, statistics showing eating disorders are underdiagnosed and undertreated in males, stories from caring for males with eating disorders, and ways to improve care. A poll asks participants about their interests and backgrounds. The presentation discusses the need for more research focused on males, training for medical professionals, and improving access to counseling, psychiatry, and treatment programs for males with eating disorders.
C-TAC 2015 National Summit on Advanced Illness Care - Master Slide Deckzbarehmi
This document provides an overview of the National Summit on Advanced Illness Care that took place on March 2-3, 2015 in Washington DC. The summit was hosted by C-TAC (Coalition to Transform Advanced Care) and brought together leaders, clinicians, researchers, and policymakers to drive improvements in advanced illness care. Over the two-day event, there were presentations on models of advanced illness care, engaging patients and families, improving clinician-patient communication, the role of research and policies to support high-quality end-of-life care for all Americans.
The document discusses developing a community profile, which is an analyzed report describing key data about a population within certain boundaries. It outlines the main purposes of a community profile, which are to collect baseline health and socioeconomic data to help plan, implement, and evaluate health programs. The document describes the different types of data that should be collected for a community profile, including demographic data, epidemiological data, health service data, and data on knowledge, attitudes, and practices of community members.
This document discusses patient-oriented research and patient engagement in health research. It defines patient-oriented research as research that engages patients as partners, focuses on patient priorities, improves outcomes, and aims to apply knowledge to improve healthcare. Patient engagement is defined as meaningful involvement of patients in governance, priority-setting, conducting, and knowledge translation of research. The document outlines guiding principles of engagement, why engagement is important, levels of engagement, and tools/resources to support engagement. It emphasizes inclusion of diverse voices and conducting research with patients, not on them.
The Finance, Audit, and Administration Committee (FAAC) reported to the PCORI Board of Governors. The FAAC recommended three nominees for the SCCOI: Dr. Bernard Lo, Arthur Levin, and Annette Bar-Cohen. The FAAC also recommended Harris Beach PLLC to serve as legal counsel to the SCCOI. In addition, the FAAC discussed GAO oversight and compliance, financial statement audits, and managing PCORI's cash flow.
Salford Jewish Community Health Research Report 2016Jonny Wineberg
This document summarizes the key findings of a research report on the health needs of Jewish communities in Salford, England. The research had five stages: 1) recruiting and training peer researchers, 2) focus groups led by peer researchers, 3) developing a quantitative survey, 4) administering the survey, and 5) creating a report and recommendations. Some initial themes from focus groups included concerns about immunizations, special educational needs assessments, and mental health services. The report provides details on demographics of survey respondents, health behaviors like fruit/vegetable and alcohol consumption, views on exercise, and hospital usage. It identifies opportunities to improve health education, access to services, and engagement between the community and NHS Salford
Improving the Family Experience at the End of Life in Organ DonationAndi Chatburn, DO, MA
Communication skills strategies for improving family experience at the end of life for patients who die in the ICU after determination of brain death or after removing mechanical life support. Audience: Organ Procurement Organization staff and hospital administration
This document provides an overview of comparative effectiveness research (CER), patient-centered outcomes research (PCOR), and the Patient-Centered Outcomes Research Institute (PCORI). It discusses the history and establishment of PCORI in 2010, its focus on patient-centered outcomes directly impacting patients' lives, and its funding priorities and first round of funded projects examining topics like treatment options, healthcare systems, communication/dissemination, and disparities. The agenda outlines a symposium focused on stakeholder engagement in CER and PCOR.
SRF Webinar: Beyond DUP - Addressing Disengagement in Community-based Early I...wef
Presentation made March 22, 2017, during the live webinar hosted by Schizophrenia Research Forum (SRF). Event recording and additional slides at http://www.schizophreniaforum.org/forums/achieving-effective-treatment-early-psychosis-united-states
Update on Personal Health Records for Developmentally Delayed Individuals: Wh...Vincent Gibbons
The document discusses the need for a personal health record (PHR) tailored for children with special healthcare needs (CSHCN). It proposes a parent-controlled PHR that would provide features like storing health information, generating reports, coordinating care among providers, and linking to educational resources. The summary identifies the key requirements of a PHR for CSHCN, including care plans, condition-specific growth charts, and financial management tools. It also notes existing PHR products and barriers to widespread adoption. The proposed PHR aims to empower parents by giving them control over their child's health information.
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Update on Personal Health Records for Developmentally Delayed Individuals: Wh...
Julliard Diversity Presentation 2013
1. Developing Diversity-
Oriented Qualitative
Research in Community
Health Care Settings
Kell Julliard, MA
Lutheran Medical Center
Brooklyn, New York
2. Qualitative Research
Methodology
• Makes sense of human experience
• Describes and explains social and cultural
influences
• Develops explanatory theories
• Explores human-oriented problems about
which little is known
3. Differences from quantitative
• Quantitative: randomized controlled trials
testing a new drug, cohort studies
assessing risk factors
Qualitative:
• Hypothesis not clear at beginning
• Means of data collection may change as
learning occurs
• Few numbers/percentages reported
• Stop when quit learning new info
• Researcher enters subjects’ world
5. Grounded theory
• Primary purpose: generate theories of
human behavior
• Theory emerges from what subjects do
and say
6. Methods of Data Gathering
• Observation/field notes
• Interviews
• Key informants
• Focus groups
7. Interviews
• Flexible and powerful tool
• Three main types: Structured, Semi-
structured, and In-depth
• Structured
– Structured questionnaire asked by trained
interviewers in standard manner
8. Interviews
• Good for sensitive topics where need for
confidentiality and trust are paramount
• Semi-structured
– Open-ended questions that define area to be
explored
• In-depth
– One or two issues covered in detail
– Questions are based on interviewees’ reply
• Various ways of recording interviews
– Notes written at the time or afterwards
– Audio or video taping
9. Interviews
• Good open ended questions assess
– Behavior or experience
– Opinion or belief
– Feelings
– Knowledge
– Demographic information
10. Key informants
• A person residing in the community
• Considered by community members to be
knowledgeable on topic
• Willing to share this information
• Each informant identifies other informants
11. Focus Groups
• Relatively homogenous groups
• Individuals share ideas about a topic
• Purpose: produce honest disclosure –
individuals need to build trust quickly so that
their sharing stimulates agreement,
disagreement, richness of information
• Size typically 7 to 10 members
• More than one focus group usually planned to
obtain diversity of opinion
• What is said in the groups is transcribed and
analyzed
12. Qualitative data analysis
• Consists of
– Data reduction
– Data display
– Conclusion drawing and verification
13. Data Reduction
• Identify themes in data
• Compare and contrast data from each
theme
• Draw conclusions
• Data display: explanatory diagrams, flow
charts, causal networks, tables of themes
with supporting quotes
14. Conclusion drawing/Verification
• Note regularities, patterns, explanations,
causal factors, and propositions
• Maintain openness and skepticism
• Conclusions become clearer as study
progresses
• Test meanings for validity as you go
15. Comparison with
quantitative analysis
• Data reduction = Computing means,
standard deviations
• Data display = tables, graphs, charts
• Conclusion = p values, experimental and
control group differences
16.
17. 99,598 people in Sunset Park
(2010 census)
Hispanic
Chinese
White
Black
Two or more
18.
19.
20.
21.
22.
23. • All studies reported here were presented
at national meetings and published
• Only one study received outside funding
24. Health needs assessment
of the Chinese Population
in Sunset Park
from a holistic perspective
Khin Kyaw Kyaw Thein, MD, Kyaw Thuya Zaw, MD, Rui-Er
Teng, MD, Celia Liang, DO,
Kell Julliard, ATR-BC
25. Team Composition
• Two MD volunteers seeking residency
• Two Chinese Family Medicine residents
needing to fulfill research requirement
• Qualitative researcher (KJ)
26. Resources needed
• Time for carrying out study
• A variety of IT reports
• Administrative support in identifying key
informants, interviewees
27. Introduction
• Growing emphasis on cultural competence
in health care delivery
• SP- bottom 10 of NY neighborhoods
• Chinese - 25% of Sunset Park residents
• Access to health care for Chinese people is
lower than those of other ethnic groups.
• Even in the Chinese, disparities exist based
on their income, immigration status, social
classes, and place of birth.
28. Introduction (cont.)
• Purpose - to identify the health needs of the
CPSP from a holistic perspective-physical, social,
mental, and spiritual points of view.
• 3 parts of the main study:
(1) Perception of health needs by Chinese
community members
(2) Comments on health related issues by health
professionals and community leaders
(3) Information from electronic databases
29. Methods
• Information from Electronic Databases
– LMC – electronic billing data
– Infoshare Online
– New York City Department of Health and
Mental Hygiene
– Epidemiology Query Survey data
– Asain American Federation of New York
• Interviews and FGD with LHC physicians,
key administrators and clinicians within LHC
system, representatives from BCAA, CPC,
American Cancer Society.
30. Methods (Cont.)
• One-on-one interview in Cantonese and
Mandarin with Chinese community
members:
– Total 37 interviews at FHC, private clinics,
school, interviewees’ homes, and public places
such as restaurants and department stores
– Interviewees: 15 to 76 yr, elderly, working age
men and women, and an adolescent, living in
US from 3 to 20 years and in Sunset Park, 5
months to 20 years.
32. Results
The combined results from three parts of the study:
• D = Information from electronic databases
• P = Information from health professional and
community leaders
• C = Information from community members
Order of presentation includes:
• Physical Health
• Mental Health
• Social Health
• Spiritual Health
• Health Seeking Behaviors
• Health Needs
33. Physical Health
Outpatients – Adults
• Normal pregnancy (D)
• Hypertension (P, C, D)
• Diabetes (P, C, D)
• Heart disease (P, C, D)
• TB (P, C)
• Hepatitis B (P, C)
• Peptic ulcer disease (P, D)
• Smoking – mostly men (P, C)
34. Physical Health (Cont.)
Top Causes of Death
• Heart disease
• Cancer
• Stroke
• Chronic lower respiratory disease
(smoking)
• Influenza and pneumonia
35. Mental Health
• Is a stigma, so do not discuss (P, C)
• Depression (P, C)
• Somatization (P) – detection low
• High stress (C)
• Anxiety (C)
• Schizophrenia (C) – high visibility
36. Social Health
Environment
• Overcrowding (C)
• Theft (C)
• Gambling (C)
• Prostitution (C)
• Dirty streets (C)
• Teenage gangs (C)
• School absenteeism, dropouts (C)
37. Social Health (Cont.)
Work
• Long working hours (C)
• Much manual labor (C, D)
• Low pay (C)
• Lack of job security (C)
• Poor work environment (C)
• Lack of health insurance (P, C)
• Language barriers (C)
38. Social Health (Cont.)
Family
• Conflicts over money
• Parents lack time to care for children
• One parent may work out of state – Child
HealthPlus only available in NY
• Infants sent to China until school age (P, C)
• Cost of childcare higher in US
• Lack of family time together
39. Social Health (Cont.)
Family
• Children lack supervision
• Children lose their Chinese language, culture &
tradition – leading to:
– Growing cultural gap between generations (P,
C)
– Miscommunications to no no communication
between generations
• Because of language problems, parents rely on
children for translation
• Conflict with in-laws
• No consensus on whether the elderly isolated or
not (P, C)
40. Spiritual Issues
• Most do not have religious or social
support (C)
• Christianity (young) and Buddhism
(elderly) – main religions (C)
• Traditional practices during holidays (C)
• Many believe spirituality influences
health (C)
41. Health-seeking behaviors
• Preferred western medicine or combined
traditional and western (P, C)
• Believe antibiotics cure almost all illnesses (P)
• Buy antibiotics OTC
• Noncompliant with doctors’ advice (P)
• Undocumented immigrants don’t seek care –
afraid of being reported (P)
• Seeking services depends on if they have health
insurance (P, C)
42. Limitations
• A small study, not representative of the
entire CPSP.
• Subjected to individual’s experience and
knowledge.
• No funding. No incentives for
interviewees.
• Difficulty to find interviewees who are
willing to volunteer their time.
• Limited time.
• Some Electronic Data – not recent.
43. Recommendations
Need more Chinese speaking health care
professionals, especially psychiatric and social
services provided in a culturally sensitive way.
More education regarding Western health care
via Chinese pamphlets, public lectures, health
fairs or newspapers.
Free screenings.
Health professionals also need to be aware of
the community members’ beliefs regarding
Western medicine versus TCM so that they can
better understand them.
Poverty creates many social and physical health
problems – difficult to solve.
44. What Latina Patients
Don’t Tell Their Doctors:
A Qualitative Study
C. Delgado, DO, E. Cruz, MD, J. Vivar
MD,
J Bellask, H Sabers, and K. Julliard, MA
Family Medicine, Internal Medicine, and the Department of
Community-Based Programs
Lutheran Medical Center 2007
45. Team Composition
• One MD volunteer seeking research
experience
• Two residents needing to fulfill research
requirement – one Internal Medicine, one
Family Medicine
• Community services support staff member
• Medical student
• Qualitative researcher (KJ)
46. Patient Disclosure
• Treatment and health affected by what
patient chooses to disclose to physician
• Culture and gender play important role in
what patients disclose
• General reasons for nondisclosure in
Latina women are not well understood
47. Goal
• To better understand factors contributing
to nondisclosure of medical information by
Latina patients to their doctors
48. Methods
• Participants
– Hispanic women living in Sunset Park
– Informed consent obtained
– Age 18 years old and older
– Primarily clients using services of our
Family Support Center
49. Interviews
• In-depth one-on-one interviews
• Trained bilingual interviewers
• Semi-structured interview guide
– Based on Sankar and Jones format
• Interviews lasted 30-60 minutes
• $25.00 payment for participating
50. Qualitative Data Analysis
• Data = transcribed interviews
• Analyzed using a grounded theory approach
(theory emerges from data)
• Interviewers and authors read transcripts of
all interviews and discussed each one
• Themes emerged from interview data
• Themes were codified into a coherent list
51. Results
• 28 interviews: 6 major themes emerged
– Physician-patient relationship
– Language barriers
– Sensitive issues
– Culture differences
– Gender and age differences
– Time constraints
52. Physician-Patient Relationship
– 26 participants commented on this theme:
– Qualities of compassion and Caring
• Domestic violence, Death issues, Fertility
– Respect and communication skills
• Decreased confidence in their doctors
• Lied about real symptoms
• Couldn’t trust physician with intimate details
53. Language Barriers
– 23 participants commented on this theme
– Physician didn’t speak Spanish
• Patient couldn’t explain needs
• Patient couldn’t understand instructions
– Use of translators
– Physician didn’t speak understandably
• Patient felt inadequate, found help elsewhere
54. Sensitive Issues
– 20 participants mentioned this theme
– Sex, sexuality and genital problems
• Lied about PAP tests, genital problems
– Reproductive issues
• Fertility, abortions, STD’s
– Violence, abuse and Drugs
• Afraid of the repercussions, the law
55. Culture
– 19 participants mentioned this theme
– Own cultural beliefs and practice
• Sex isn’t discussed in public
• Family problems stay in the family
– Doctors’ cultural beliefs
• Attitudes not conducive to trust
• Judgmental attitudes : STD’s, Abortions
56. Gender and Age Differences
– 13 participants mentioned this theme
– Age of the physician was less common
• Sexuality issues - embarrassing
– Gender of the physician more common
• Won’t talk about sex with male physician
• Won’t talk about reproductive issues
• Don’t want to be examined by males
57. Time Constraints
– 7 participants commented on this theme
– Visits are too short
– Hindered development of doctor/patient
relationship
– Uncomfortable with their physicians
– Doctors cut them off
– Don’t listen to their needs
– Patients use limited time to hide information
58. Health Assessment of the
Arab American Community
in Southwest Brooklyn
Kell Julliard, Linda Sarsour, Virginia Tong,
Omar Jaber, and Mohammed Talbi
Arab American Association of New York
Lutheran HealthCare
Brooklyn, New York
59.
60.
61.
62.
63. Team Composition
• Member of AAANY staff
• VP for cultural comptence
• Health center Arabic liaison
• Arabic college student
• Qualitative researcher (KJ)
64. Community Partners
• Arab American Association of New York
• New York City Council – modest funding
• Lutheran Medical Center
• Lutheran Family Health Centers
65. Resources
• Health access, status, and demographic
survey created jointly between AAANY
and health center
• AAANY provided staff to conduct survey
and organized presence at events
• Health center provided research/survey
expertise, training in qualitative and
structured survey interviewing, support in
scanning survey, data analysis, writing
and presenting
66. Introduction
• “Racial and ethnic minorities tend to
receive a lower quality of health care than
non-minorities, even when access-related
factors, such as a patient’s insurance
status and income are controlled.” –
Smedley et al, 2002
• Arab Americans – part of this low-income
group not receiving appropriate health
care?
67. ACCESS surveys suggest
• high prevalence of chronic diseases
• underuse of health services
• limited preventive health practices
• ACCESS = Arab Community Center for
Economic and Social Services
68. In the Arab world
• Life expectancy –
– 62.6 years for men
– 65.2 years for women
• About 10 years less than for US adults
69. Objective
• To gather basic demographic information
about the Arab American community in
Brooklyn
• To assess members’ perceptions of health
status, needs, behaviors, and access to
services
70. Such a survey could provide
• Direction for implementing changes in the
health care system
• More culturally competent care for this
population
• Improved access to care
• Better planning and evaluation of service
programs specific to Arab Americans
71. Lutheran HealthCare
Lutheran Medical Center
Lutheran Family Health
Centers
• Arabic-speaking bilingual
bicultural staff
• Arab patient representative
• Free interpretation services
• Halal meals available
• Onsite Mosque
• Signage and written
documents in Arabic
• Imam on call service
72. Methods
• Study designed and implemented through
a collaborative partnership:
• Arab American Association of New York
(AAANY)
• Lutheran HealthCare (LHC)
73. Survey
l Written in English
l Translated into Arabic by AAANY
l Respondents could be interviewed in
either language
74. Implementation
l Survey conducted in April and May of
2008
l Interviewers trained in non-biased
techniques
l Participants interviewed individually
l At Arab community gathering places in
southwest Brooklyn
l Convenience sample
75.
76. Survey respondents
• 348 respondents
– 200 women
– 148 men
• Reflected southwest Brooklyn
• Most frequent countries of immigration:
Egypt, Yemen, Morocco, Palestine
• 88% Muslim
• 92% primarily spoke Arabic at home
• 56% moved to US before 2000
77. • 58% chose health care venue based on
language
• The rate of poverty
– 42% in this sample of Arab Americans
– 16% in southwest Brooklyn overall
• No health insurance
– 37% who moved to US after 1999
– 21% who moved to US 1999 and before
• Almost half of respondents never
exercised
78. Percentage uninsured
l 28% of this sample of Arab Americans
l 22% of immigrants in New York City
overall
l 18% of New York City overall
l 18% of Brooklyn overall
l 13% of Southwest Brooklyn overall
79. Foreign-Born vs. US-Born Adults
Rating Their Health Status
Fair/Poor
40 36
31
30 Total
30 24 26 Hispanic
2019 21
20 16 17 Asian
12 White
10 Arab overall
0 Black
Foreign-born US-born
80. Comparison of Arab Americans
with NYC Overall
45 42
40
35
30 28
Percentage
25
22
21
Arab-Americans
20
New York City
15
10
5
0
Living in Poverty Uninsured
81. Employment (p < 0.001)
Men Women
59% employed full time 8%
17% employed part time 10%
17% unemployed 28%
1% homemakers 45%
82. Smoking in Arab Men vs. Immigrant Men in
NYC
45
42
40
35
Percentage
30
25 Arab
25
21 Russian
20 Mexican
20
17 Chinese
15 Jamaican
10
5
0
Smoker
83. Discussion
l Compared to other immigrant men and
Arab American women in NYC our
findings suggest that Arab men in
Southwest Brooklyn have a much higher
rate of smoking.
l Survey assessed cigarette smoking.
Numbers of other forms of smoking could
be much higher – e.g., hookah smoking.
84. • The health impact of smoking and poverty
on the Arab American community in
Southwest Brooklyn is cause for concern.
• Future research should quantify these
issues more precisely so that effective
programs can be designed and funded.
85. Parental attitudes on feeding, oral
hygiene, and dental treatment of
children in the Chinese population
with Early Childhood Caries- A
Qualitative Research Project
Diane Wong, D.D.S, Silvia Perez-Spiess and
Kell Julliard
Lutheran Medical Center, Brooklyn, New York
86.
87. Team Composition
• Pediatric Dentistry resident needing to
fulfill research requirement
• Experienced pediatric dentist
• Qualitative
researcher (KJ)
88. Introduction
• Many Chinese children in dental clinic had
multiple carious teeth, were diagnosed
with Early Childhood Caries (ECC).
• Some received dental treatment under
general anesthesia or sedation because
extensive treatment needed or were
uncooperative.
• Cultural beliefs and attitudes may affect
the development and progression of this
problem.
89. Objective
• To learn about the Chinese parents’ unique
perspective regarding Early Childhood Caries in
their children.
• Parents encouraged to share their views
regarding oral hygiene habits, cultural beliefs,
and attitudes towards dental treatment.
• Findings will enable providers to have better
understanding and be able to provide more
culturally sensitive care.
90. Methods
• Individual interviews with parents
• Sample - 20 parents and one grandparent
• Each one-hour interview tape-recorded and later
transcribed.
• Interviews conducted in child’s home or hospital
depending on the parents’ preference.
• Cantonese, Mandarin, or English language used during
the interview.
• Each parent - small monetary gift along with
toothbrushes and toothpaste.
• Interview guide covered oral hygiene and habits,
parental attitudes on dental problems, and cultural
beliefs regarding dental treatment.
91. Results – Negative Themes
• Fears of dental anesthesia, lack of social
support in seeking dental treatment, inadequate
knowledge of good oral hygiene and habits, and
cultural beliefs that do not support the practice of
preserving a healthy primary dentition
– Parents think that general anesthesia will negatively
affect the development of the child’s brain.
– Grandparents scold the parents for allowing their
children to have surgery simply to fix baby teeth.
– Parents often do not brush their children’s teeth
regularly because they did not do so as children.
– Friends shocked when see that parents allowed
multiple extractions to be done at once. They feel that
these procedures are bad for the child.
92. Positive themes
• Trust in the providers, satisfaction with outcome
of dental treatment, and improved understanding
of oral health.
– Parents feel that technology in the Western world is
more advanced than in China. They are glad that their
children received this dental treatment efficiently in
the hospital.
– Although many parents use Chinese herbal remedies
to address their own dental problems, they most often
turn to Western medicine when their children need
treatment.
– Parents accepted the recommendations given to
them by the dentists and they feel that it is important
to free their children from dental caries and pain, and
maintaining oral health is essential.
93. Conclusions
• Many parents unaware of optimal oral hygiene habits
and feeding habits partially because they grew up in a
time and place where the society and culture that did not
focus on preservation of the primary dentition.
• Although many parents expressed fear and concern as
their children were in the process of receiving dental
care, the majority felt that they had made the right
decision in proceeding with the treatment regardless of
other people’s negative opinions.
• The society including friends, family members, and
community bring negative influences to these parents.
• Healthcare providers can now anticipate what beliefs
common to this community, can better recognize
problems and begin intervention at earlier stage.
94. Recommendations to dental
healthcare providers
• Provide education (written, verbal or visual) to
parents and caregivers on the importance of
preserving and maintaining a healthy primary
dentition in preferred language.
• Understand the parent’s cultural beliefs and
backgrounds.
• Reassure parents of the benefits that treatment
will provide for primary and permanent dentition.
• Maintain the importance of good oral hygiene,
good diet, and regular recall visits.
• Educate Chinese community in general
95. Our ways of sharing findings of
qualitative studies
• Annual health system-wide research fair
• Departmental conferences
• Online newsletter
• Task force meetings
• Summaries circulated by administration
• National and regional conferences
96. Tips for training interviewers
• Schedule dedicated training time
• Explain principles
• Opportunity for role playing
• Simulate actual interview set-up
97. Tips for Publishing Findings
• Pick journal ahead of time
• Design study in a way similar to those
previously published in journal
– Medical journals: theoretical model for
research not so important
– Academic and social science-oriented
journals: require a specific model
Qualitative research in dentistry helps us make sense of human experience with respect to oral health. It can describe and explain social and cultural influences on health care and develop explanatory theories about those. Pimarily, it explores human-oriented problems about which little is known – thus, the tools of qualitative research help us find out what people are thinking and feeling about something, but not how many people think and feel that way.
Qualitative and quantitative research are dramatically different. In qualitative research, because it’s investigating something that we don’t know much about, the hypothesis is not clear at the beginning of the research process. Similarly, the means of collecting data may change as learning occurs. Few numbers and percentages are reported, because they are not the prime focus of the research. Finally, rather than collecting data from a pre-arranged number of subjects as we do in quantitative research, we stop collecting data in qualitative research only when quit gaining new information. The goal is not for the researcher to be objective, but for him or her to deeply enter the subjects’ world and understand it from the inside.
We’ll talk about 3 theoretical approaches to qualitative research: grounded theory, ethnography, and phenomenology.
The primary purpose of grounded theory is to generate theories of human behavior. But theory does not create the research – rather, it emerges from what subjects do and say.
Ethnography tends to rely on in-person observations and field notes. Other forms of qualitative research rely more on interviews of various kinds. They may be in-depth, one-on-one interviews with key informants, or interviews with groups called focus groups.
Interviews form a flexible and powerful tool for qualitative exploration. They have three main types: structured, semi-structured, and in-depth. Structured questionnaires consists of questions asked by trained interviewers in standard manner. They are actually not a part of qualitative research, but they may be conducted in person.
In semi-structured interviews, the interviewer asks open-ended questions that define the areas to be explored. The questions may vary from interview to interview depending on the information disclosed by the subject. In-depth interviews probe one or two issues in detail. Their questions are mostly based on interviewees’ replies to being asked about the issues under investigation. There are various ways of recording interviews. Notes can be written at the time (if you are a fast writer) or afterwards. The best thing to do is audio- or video-tape the interview. Or have a second person take detailed notes. Then you can devote all your attention to the interview process itself.
Interviews rely on open ended questions to assess factors such as behavior or experience, opinion or belief, feelings, knowledge, and even demographic information.
Key informants are especially good persons to interview in qualitative research. They are persons who are part of the community in question and who are considered by community members to be knowledgeable on the particular topic. They must be willing to share this information. Informants can help identify other informants.
One-on-one interviews are best when the topic in question is sensitive and people aren’t likely to share in a group. But if additional persons are likely to stimulate the sharing of richer information, then a focus group is called for. Focus groups are relatively homogenous groups in which individuals share ideas about a topic. They typically contain 7 to 10 members. More than one focus group is usually planned to obtain a diversity of opinion. What is said in the groups is transcribed and analyzed
Qualitative data collection results in a large volume of data – consisting of everything that was said and done in the interviews and focus groups. This data needs to be reduced or boiled down to its most important elements. Sometimes diagrams and figures help to organize the data, just as graphs do in quantitative research. Based on these important elements and relationships, conclusions are drawn.
Data reduction primarily consists of identifying the important themes in the data. What is said about each theme is then compared and contrasted according to who is speaking. For instance, patients who are immigrants may believe one thing, and patients who were born in the US may believe another. Being able to contrast these beliefs could be important to patient compliance. The researchers then draw conclusions based on the comparisons and contrasts within the various themes.
The study’s conclusions often note regularities, patterns, explanations, and causal factors related to the theme of the research. The researchers maintain openness and skepticism as they collect their data. Because the data analysis is occurring while the data collection progresses, the study’s conclusions become clearer as it progresses. The researchers can then test meanings and themes for validity as they go.
In some ways the structure of qualitative data analysis is very much like that of quantitative analysis. Qualitative data reduction is equivalent to computing means and standard deviations in quantitative research. Data display is similar to creating tables, graphs, and charts. The overall conclusions of qualitative research are similar to quantitative research’s p values and the differences reported between the experimental and control groups.