An overview of how research questions are generated, how research is conducted, and disseminated to benefit the creation of interventions to reduce colorectal cancer among African American women.
A randomized controlled trial of the bruthas programCAPSUCSF
This study is a randomized controlled trial that will compare an enhanced HIV counseling intervention called the Bruthas Program to a standard HIV counseling and testing program. The trial aims to recruit 400 African American men who have sex with men but do not identify as gay from the San Francisco Bay Area. Participants will be randomly assigned to receive either the enhanced counseling intervention focusing on identity, safer sex skills, and regular HIV testing or the standard program. The effectiveness of the enhanced intervention will be evaluated based on whether it reduces sexual risk behavior more than the standard program based on behavioral assessments at 6 and 9 month follow ups.
FactSheet-GMaPContact Revised 9-23-2016GMaP Region 2
The Geographic Management of Cancer Health Disparities Program (GMaP) employs a systematic strategy to build regional "hubs" or networks across the United States to support and manage cancer and health disparities research, training, and infrastructure. GMaP involves over 1,200 researchers, trainees, and educators across its 7 regions. It aims to foster collaboration among these groups and contribute to the science around cancer and health disparities, promote training of underrepresented investigators, and enhance access to cancer information and research for underserved communities. GMaP provides resources such as informational webinars, mentoring connections, funding opportunities, and grant writing workshops to help achieve these goals.
This document summarizes a study on gynecologic cancers in rural areas of Kenya. The study aimed to understand the knowledge, myths, and screening practices around cervical, breast, and prostate cancers. It found that many rural Kenyans are unaware of routine cancer screening and do not utilize screening services due to stigma and cost concerns. Major barriers to screening included ignorance, myths, illiteracy, lack of perceived risk, and financial constraints. The study recommends increased public education on cancer prevention, screening, nutrition, and signs; and making affordable screening services more available locally.
Gay Poz Sex: A Community Based Counselling Intervention for HIV positive gay/...CBRC
GPS is a community-based counselling program for HIV-positive gay and bisexual men that aims to decrease sexual health risks and improve sex and well-being through a peer-led, theoretically grounded intervention. The program is based on models of information, motivation, and behavioral skills, and uses motivational interviewing techniques over multiple sessions to help participants set and achieve risk reduction goals in a supportive environment. Preliminary research found the program increased participants' sense of agency regarding their sexual health, social support systems, and confidence making healthier choices.
Ruth Buzi of the Baylor College of Medicine Teen Health Clinic higlights an array of social media strategies used to enhance health promotion among youth and young adults. Presented at YTH Live 2014 session "The Strength of Social Media."
Friends, Follows and Retweets: The Impact of Social Media on Patients and Pro...Michelle Catalano
This document discusses the importance and popularity of social media in healthcare. It describes how patients and providers are increasingly using social media tools like Facebook, Twitter, YouTube and text messaging to communicate about health issues. For patients, social media allows them to obtain health information and find support from others dealing with similar conditions. The document advises healthcare organizations to develop social media policies that address goals, audiences, responsibilities and appropriate content when using these tools.
A randomized controlled trial of the bruthas programCAPSUCSF
This study is a randomized controlled trial that will compare an enhanced HIV counseling intervention called the Bruthas Program to a standard HIV counseling and testing program. The trial aims to recruit 400 African American men who have sex with men but do not identify as gay from the San Francisco Bay Area. Participants will be randomly assigned to receive either the enhanced counseling intervention focusing on identity, safer sex skills, and regular HIV testing or the standard program. The effectiveness of the enhanced intervention will be evaluated based on whether it reduces sexual risk behavior more than the standard program based on behavioral assessments at 6 and 9 month follow ups.
FactSheet-GMaPContact Revised 9-23-2016GMaP Region 2
The Geographic Management of Cancer Health Disparities Program (GMaP) employs a systematic strategy to build regional "hubs" or networks across the United States to support and manage cancer and health disparities research, training, and infrastructure. GMaP involves over 1,200 researchers, trainees, and educators across its 7 regions. It aims to foster collaboration among these groups and contribute to the science around cancer and health disparities, promote training of underrepresented investigators, and enhance access to cancer information and research for underserved communities. GMaP provides resources such as informational webinars, mentoring connections, funding opportunities, and grant writing workshops to help achieve these goals.
This document summarizes a study on gynecologic cancers in rural areas of Kenya. The study aimed to understand the knowledge, myths, and screening practices around cervical, breast, and prostate cancers. It found that many rural Kenyans are unaware of routine cancer screening and do not utilize screening services due to stigma and cost concerns. Major barriers to screening included ignorance, myths, illiteracy, lack of perceived risk, and financial constraints. The study recommends increased public education on cancer prevention, screening, nutrition, and signs; and making affordable screening services more available locally.
Gay Poz Sex: A Community Based Counselling Intervention for HIV positive gay/...CBRC
GPS is a community-based counselling program for HIV-positive gay and bisexual men that aims to decrease sexual health risks and improve sex and well-being through a peer-led, theoretically grounded intervention. The program is based on models of information, motivation, and behavioral skills, and uses motivational interviewing techniques over multiple sessions to help participants set and achieve risk reduction goals in a supportive environment. Preliminary research found the program increased participants' sense of agency regarding their sexual health, social support systems, and confidence making healthier choices.
Ruth Buzi of the Baylor College of Medicine Teen Health Clinic higlights an array of social media strategies used to enhance health promotion among youth and young adults. Presented at YTH Live 2014 session "The Strength of Social Media."
Friends, Follows and Retweets: The Impact of Social Media on Patients and Pro...Michelle Catalano
This document discusses the importance and popularity of social media in healthcare. It describes how patients and providers are increasingly using social media tools like Facebook, Twitter, YouTube and text messaging to communicate about health issues. For patients, social media allows them to obtain health information and find support from others dealing with similar conditions. The document advises healthcare organizations to develop social media policies that address goals, audiences, responsibilities and appropriate content when using these tools.
1) The document describes a multi-disciplinary service learning program called ¡Una Vida Sana! (UVS) that provides health screenings to Richmond, Virginia's Hispanic community.
2) UVS is a collaboration between VCU's schools of medicine, nursing, and pharmacy that aims to assess the health status and improve access to care for Hispanics in Richmond.
3) Preliminary results from UVS screenings suggest that while patients do not yet have high rates of disease, they are at risk for developing cardiovascular and metabolic conditions in the future. The program aims to strengthen its service learning model and increase its capacity to serve more students and community members.
Central PA 2014 Healthcare Odyssey PanelistsBenjamin Pease
The document outlines the agenda for the 2014 Healthcare Odyssey conference, including panels on CEO issues, para medicine, social media, and long term care. It also discusses a keynote presentation on the Choosing Wisely initiative, which challenges medical specialties to identify unnecessary treatments and tests. The initiative aims to empower patients and encourage evidence-based medicine, though questions remain around its realistic impact. The agenda then lists moderator and panelist names and titles for each session.
This document discusses the Collaboration for Outcomes Using Social Media in Oncology (COSMO), a group of oncologists and hematologists who are exploring the use of social media in cancer care. COSMO aims to define best practices for social media use, conduct research on its benefits and limitations, and enhance communication within the oncology community and between doctors and patients. Some of COSMO's accomplishments include promoting hashtags for online discussions, publishing reviews on social media risks/benefits, and conducting qualitative Twitter chat research to understand patient needs. The collaboration is important because patients often look to doctors for cancer information online.
The document discusses engaging with patients and the public through social media. It notes that the most trusted forms of advertising now come through personal recommendations, online consumer opinions, and branded websites, all promoted through social media. It provides statistics showing that most people in the UK have social media accounts and prefer engaging with organizations through social media over visiting physical locations. The Mayo Clinic is highlighted as a leader in using social media to improve health globally and spur deeper engagement through social media. The document advocates connecting with the 3% of people in an organization or system that influence 85% of others through social media.
Rates of breast cancer are increasing in rural China, projected to reach 100 cases per 100,000 women aged 55-69 by 2021. This is attributed to poor diet, pollution exposure, and tobacco/alcohol use. The document proposes several initiatives to address this through education on prevention, screening and early detection, and patient support. It discusses developing low-cost screening options and an outreach campaign to disperse information in rural areas, noting challenges around health messaging and developing affordable solutions within financial constraints. Key research areas are a lack of healthcare information in rural communities and links between lifestyle, genetics, and breast cancer risk.
What do patients' need, right now, at this very given moment? It's an excellent question, which--if we mean to actually achieve--we should narrow down to a few concise and relevant points.
Paramount to the deconstruction of patient needs is understanding what the goal for patients is. This goal isn't just to live. It's to live well. It's to contribute to and enjoy the world -- to have hike the mountains, enjoy the breeze of the oceans, bask in the heat, laugh with friends, love our partners, and grow as a person.
Now, moving slowly from the goal to the respective problems. We have patients who are ill once or twice and are then relatively healthy, healthy patients who see their doctor once a year for a checkup, chronically ill people who live for the rest of their life with chronic conditions like Crohn's or Hyperthyroidism, and there are terminal patients dealing with life threatening illnesses. Certainly, there are many many more subsections of patients.
The needs for each of these segments are varient - varying along a spectrum with healthy patients needing less than the chronic and the chronic needing less than the terminal. Some people happen to be further along this spectrum than others. At the end of this presentation, we announced a survey to enumerate and articulate these needs across these various spectrums. It is our hope that this survey helps illustrate these pieces along the timeline, allowing us to focus on perfecting each piece.
Summer 2017 I served as the Development Intern for Gateway to Hope, a non-profit serving breast cancer patients. I was given the opportunity to present on the internship at the Missouri Public Health Association Conference in September 2017, and at the Missouri Association for Health, Physical Education, Recreation and Dance Conference in November 2017.
This document proposes solutions to address the growing rates of breast cancer in rural China. It aims to provide education on breast cancer causes and prevention, offer screening resources, and support patient communities. Key challenges include effective information dispersal in rural areas and developing affordable screening. Research found lack of healthcare information and links between lifestyle, diet, and cancer. The proposal is a mobile clinic with examination rooms, medical equipment, and telemedicine for education, primary care, screening, and treating simple diseases. Shipping containers are suggested for their sustainability, low-cost, and adaptability.
The document summarizes the journey of a public health cohort from the Bay Mills Indian Community who participated in an education and training program at the University of Nevada Las Vegas. The cohort learned about public health concepts and tools, conducted a community health survey of tribal youth, and developed two action plans to promote the Boys and Girls Club and higher education in the community. They implemented their plans at local health fairs and schools.
This document describes a study that aims to understand factors contributing to healthcare utilization disparities in African American males with Hepatitis C virus (HCV) through qualitative interviews. The study will collect feedback from African American males with HCV to explore individual, social, and health system barriers to HCV care and treatment. The researchers will then develop and pilot test culturally tailored intervention messages to improve linkage to and retention in HCV care. The goal is to understand determinants of HCV healthcare utilization in order to generate effective health promotion strategies for this at-risk population.
This document describes a study to improve diabetes medication management for African American men through pharmacist-facilitated face-to-face and online support groups. The study involves two locations with 5 cohorts of 10 participants each, for a total of 100 participants. The support groups will have an initial and final face-to-face session with 10 weeks of online discussions in between. The study aims to assess the impact on participants and determine the feasibility and acceptability of the intervention through surveys and interviews. Enrollment is ongoing and initial support groups have started with data analysis planned for summer 2016.
This document summarizes efforts to conduct large-scale clinical genomics studies by directly partnering with and engaging cancer patients. It describes three projects - the Metastatic Breast Cancer Project, Angiosarcoma Cancer Project, and Metastatic Prostate Cancer Project - that have directly enrolled thousands of cancer patients to provide clinical, genomic, and patient-reported data through social media and at-home sample collection kits. Key lessons highlighted include engaging patients throughout the research process, making the studies inclusive and accessible to patients, and maintaining authentic interactions with patients online and in-person to build trust and partnerships.
Mobile clinic breast_cancer_research_proposal_klee4vp
This document summarizes a design project for a mobile breast cancer clinic for rural areas of China. The key points are:
- Rates of breast cancer are increasing in China due to changes in diet, pollution exposure, tobacco and alcohol use.
- The goals of the project are to raise awareness, provide prevention and early diagnosis resources, and support for patients.
- Research found a lack of healthcare information in rural areas and that lifestyle and diet are closely linked to breast cancer. The proposal is for a mobile, self-sustaining clinic that can accommodate screening and tele-consultation services.
Presentation given my 2 bright medical students; S.
WANJARA, M.MURGOR in Kenya about the awareness of cervical cancer in Kenya. Data powered by http://diy.msurvey.co.ke
Psychosocial And Behavioral Factors Related To The Post Partum97umbcpsych308
This study examined psychosocial and behavioral factors related to whether infants born to cocaine-using women were placed in custody after birth or remained with their mothers. The researchers hypothesized that women who lost custody would report higher psychological distress, more violent partner relationships, poorer coping skills, less social support, and more childhood trauma. They also hypothesized that greater prenatal cocaine use and more psychological distress would increase the likelihood of child placement. The study found that women who lost custody had fewer prenatal care visits, heavier cocaine use, and more psychological distress than women who retained custody.
Bay Area Physicians Rate Communication with UCSF Department of RadiologyLaurel Skurko
The UCSF Department of Radiology conducted a survey of 5,100 local referring physicians to understand their communication patterns and preferences. The survey found that 56% would like regular communications about department news and services, with 40% preferring email. While social media use was currently low, Facebook, LinkedIn and Twitter were the most commonly used platforms. Over 70% of respondents were satisfied with UCSF imaging services, and the top topics of interest were ultrasound, abdominal imaging, and neuroimaging. Feedback will help the department better focus communications and promote their services.
Administration Of The Hpv Vaccine In Womens Health ClinicsJolene Bethune
The document discusses educating mothers and adolescent clients about HPV and promoting HPV vaccination in women's health clinics. HPV is very common among adolescents and can cause genital warts and cervical cancer. The HPV vaccine effectively protects against the types that cause most warts and cancer. The document recommends educating clients about HPV and susceptibility during adolescence, and vaccinating girls ages 11-26 to prevent infection.
Gender in Climate Change Agriculture and Food SecurityIFPRI-PIM
This poster was presented by Sophia Huyer (CCAFS / CIAT) for the pre-Annual Scientific Conference meeting organized for the CGIAR research program gender research coordinators on 4 December.
The annual scientific conference of the CGIAR collaborative platform for gender research took place on 5-6 December 2017 in Amsterdam, the Netherlands, where the Platform is hosted (by KIT Royal Tropical Institute).
Read more: http://gender.cgiar.org/gender_events/annual-scientific-conference-capacity-development-workshop-cgiar-collaborative-platform-gender-research/
Role of Social Media in Oral and Maxillofacial SurgerySapna Vadera
The document discusses the role of social media in oral and maxillofacial surgery. It begins by introducing social media and its impact on how doctors and patients interact. It then provides statistics on social media usage among the general public and medical professionals. The main roles and uses of social media for patients and surgeons are described, such as patients using it to research procedures and surgeons using it for continuing education and professional networking. Potential drawbacks like misinformation and privacy issues are covered. Guidelines for surgeons' appropriate social media use are presented. The conclusion emphasizes that social media is becoming more important for engaging with patients, education, and the future of the field.
This program developed and delivered a computer literacy curriculum for promotores/community health workers along the Arizona-Mexico border to help address breast cancer knowledge gaps. A total of 17 promotores participated in the program, which included an initial assessment of their computer skills and informational needs. Based on the results, a 6-session curriculum was created covering basic computer skills, finding reliable health information online, website evaluation, and using resources to create educational materials for their communities. Post-training evaluations found that the promotores improved their computer skills and felt better prepared to address breast cancer in their work. Future iterations of the program will deliver more content online and utilize social media.
The meeting discussed increasing rates of early-age onset colorectal cancer (EAO CRC) and summarized efforts to address this trend. Major topics included identifying priority risk factors for EAO CRC like diet, antibiotics and obesity during childhood for further study. Participants agreed to explore relationships between these factors and the microbiome, and develop prospective cohort studies to examine incidence and adenoma outcomes. Next steps involve continued collaboration to seek funding and publish findings to inform further research.
- Melva Covington of Sanofi discusses strategies for increasing diversity in clinical trials to better represent populations impacted by medical conditions. Currently, racial and ethnic minorities are underrepresented in trials compared to disease prevalence.
- Covington emphasizes the importance of early and sustained engagement with advocacy groups and communities to build trust and partnerships for recruitment and retention. She also stresses using diverse recruitment strategies and culturally competent materials.
- Efforts are underway across the industry and with groups like the FDA to improve representation and data collection in trials through initiatives like standardizing methods and increasing proportional representation. However, more work remains to modernize clinical trials and ensure underserved populations are meaningfully included.
1) The document describes a multi-disciplinary service learning program called ¡Una Vida Sana! (UVS) that provides health screenings to Richmond, Virginia's Hispanic community.
2) UVS is a collaboration between VCU's schools of medicine, nursing, and pharmacy that aims to assess the health status and improve access to care for Hispanics in Richmond.
3) Preliminary results from UVS screenings suggest that while patients do not yet have high rates of disease, they are at risk for developing cardiovascular and metabolic conditions in the future. The program aims to strengthen its service learning model and increase its capacity to serve more students and community members.
Central PA 2014 Healthcare Odyssey PanelistsBenjamin Pease
The document outlines the agenda for the 2014 Healthcare Odyssey conference, including panels on CEO issues, para medicine, social media, and long term care. It also discusses a keynote presentation on the Choosing Wisely initiative, which challenges medical specialties to identify unnecessary treatments and tests. The initiative aims to empower patients and encourage evidence-based medicine, though questions remain around its realistic impact. The agenda then lists moderator and panelist names and titles for each session.
This document discusses the Collaboration for Outcomes Using Social Media in Oncology (COSMO), a group of oncologists and hematologists who are exploring the use of social media in cancer care. COSMO aims to define best practices for social media use, conduct research on its benefits and limitations, and enhance communication within the oncology community and between doctors and patients. Some of COSMO's accomplishments include promoting hashtags for online discussions, publishing reviews on social media risks/benefits, and conducting qualitative Twitter chat research to understand patient needs. The collaboration is important because patients often look to doctors for cancer information online.
The document discusses engaging with patients and the public through social media. It notes that the most trusted forms of advertising now come through personal recommendations, online consumer opinions, and branded websites, all promoted through social media. It provides statistics showing that most people in the UK have social media accounts and prefer engaging with organizations through social media over visiting physical locations. The Mayo Clinic is highlighted as a leader in using social media to improve health globally and spur deeper engagement through social media. The document advocates connecting with the 3% of people in an organization or system that influence 85% of others through social media.
Rates of breast cancer are increasing in rural China, projected to reach 100 cases per 100,000 women aged 55-69 by 2021. This is attributed to poor diet, pollution exposure, and tobacco/alcohol use. The document proposes several initiatives to address this through education on prevention, screening and early detection, and patient support. It discusses developing low-cost screening options and an outreach campaign to disperse information in rural areas, noting challenges around health messaging and developing affordable solutions within financial constraints. Key research areas are a lack of healthcare information in rural communities and links between lifestyle, genetics, and breast cancer risk.
What do patients' need, right now, at this very given moment? It's an excellent question, which--if we mean to actually achieve--we should narrow down to a few concise and relevant points.
Paramount to the deconstruction of patient needs is understanding what the goal for patients is. This goal isn't just to live. It's to live well. It's to contribute to and enjoy the world -- to have hike the mountains, enjoy the breeze of the oceans, bask in the heat, laugh with friends, love our partners, and grow as a person.
Now, moving slowly from the goal to the respective problems. We have patients who are ill once or twice and are then relatively healthy, healthy patients who see their doctor once a year for a checkup, chronically ill people who live for the rest of their life with chronic conditions like Crohn's or Hyperthyroidism, and there are terminal patients dealing with life threatening illnesses. Certainly, there are many many more subsections of patients.
The needs for each of these segments are varient - varying along a spectrum with healthy patients needing less than the chronic and the chronic needing less than the terminal. Some people happen to be further along this spectrum than others. At the end of this presentation, we announced a survey to enumerate and articulate these needs across these various spectrums. It is our hope that this survey helps illustrate these pieces along the timeline, allowing us to focus on perfecting each piece.
Summer 2017 I served as the Development Intern for Gateway to Hope, a non-profit serving breast cancer patients. I was given the opportunity to present on the internship at the Missouri Public Health Association Conference in September 2017, and at the Missouri Association for Health, Physical Education, Recreation and Dance Conference in November 2017.
This document proposes solutions to address the growing rates of breast cancer in rural China. It aims to provide education on breast cancer causes and prevention, offer screening resources, and support patient communities. Key challenges include effective information dispersal in rural areas and developing affordable screening. Research found lack of healthcare information and links between lifestyle, diet, and cancer. The proposal is a mobile clinic with examination rooms, medical equipment, and telemedicine for education, primary care, screening, and treating simple diseases. Shipping containers are suggested for their sustainability, low-cost, and adaptability.
The document summarizes the journey of a public health cohort from the Bay Mills Indian Community who participated in an education and training program at the University of Nevada Las Vegas. The cohort learned about public health concepts and tools, conducted a community health survey of tribal youth, and developed two action plans to promote the Boys and Girls Club and higher education in the community. They implemented their plans at local health fairs and schools.
This document describes a study that aims to understand factors contributing to healthcare utilization disparities in African American males with Hepatitis C virus (HCV) through qualitative interviews. The study will collect feedback from African American males with HCV to explore individual, social, and health system barriers to HCV care and treatment. The researchers will then develop and pilot test culturally tailored intervention messages to improve linkage to and retention in HCV care. The goal is to understand determinants of HCV healthcare utilization in order to generate effective health promotion strategies for this at-risk population.
This document describes a study to improve diabetes medication management for African American men through pharmacist-facilitated face-to-face and online support groups. The study involves two locations with 5 cohorts of 10 participants each, for a total of 100 participants. The support groups will have an initial and final face-to-face session with 10 weeks of online discussions in between. The study aims to assess the impact on participants and determine the feasibility and acceptability of the intervention through surveys and interviews. Enrollment is ongoing and initial support groups have started with data analysis planned for summer 2016.
This document summarizes efforts to conduct large-scale clinical genomics studies by directly partnering with and engaging cancer patients. It describes three projects - the Metastatic Breast Cancer Project, Angiosarcoma Cancer Project, and Metastatic Prostate Cancer Project - that have directly enrolled thousands of cancer patients to provide clinical, genomic, and patient-reported data through social media and at-home sample collection kits. Key lessons highlighted include engaging patients throughout the research process, making the studies inclusive and accessible to patients, and maintaining authentic interactions with patients online and in-person to build trust and partnerships.
Mobile clinic breast_cancer_research_proposal_klee4vp
This document summarizes a design project for a mobile breast cancer clinic for rural areas of China. The key points are:
- Rates of breast cancer are increasing in China due to changes in diet, pollution exposure, tobacco and alcohol use.
- The goals of the project are to raise awareness, provide prevention and early diagnosis resources, and support for patients.
- Research found a lack of healthcare information in rural areas and that lifestyle and diet are closely linked to breast cancer. The proposal is for a mobile, self-sustaining clinic that can accommodate screening and tele-consultation services.
Presentation given my 2 bright medical students; S.
WANJARA, M.MURGOR in Kenya about the awareness of cervical cancer in Kenya. Data powered by http://diy.msurvey.co.ke
Psychosocial And Behavioral Factors Related To The Post Partum97umbcpsych308
This study examined psychosocial and behavioral factors related to whether infants born to cocaine-using women were placed in custody after birth or remained with their mothers. The researchers hypothesized that women who lost custody would report higher psychological distress, more violent partner relationships, poorer coping skills, less social support, and more childhood trauma. They also hypothesized that greater prenatal cocaine use and more psychological distress would increase the likelihood of child placement. The study found that women who lost custody had fewer prenatal care visits, heavier cocaine use, and more psychological distress than women who retained custody.
Bay Area Physicians Rate Communication with UCSF Department of RadiologyLaurel Skurko
The UCSF Department of Radiology conducted a survey of 5,100 local referring physicians to understand their communication patterns and preferences. The survey found that 56% would like regular communications about department news and services, with 40% preferring email. While social media use was currently low, Facebook, LinkedIn and Twitter were the most commonly used platforms. Over 70% of respondents were satisfied with UCSF imaging services, and the top topics of interest were ultrasound, abdominal imaging, and neuroimaging. Feedback will help the department better focus communications and promote their services.
Administration Of The Hpv Vaccine In Womens Health ClinicsJolene Bethune
The document discusses educating mothers and adolescent clients about HPV and promoting HPV vaccination in women's health clinics. HPV is very common among adolescents and can cause genital warts and cervical cancer. The HPV vaccine effectively protects against the types that cause most warts and cancer. The document recommends educating clients about HPV and susceptibility during adolescence, and vaccinating girls ages 11-26 to prevent infection.
Gender in Climate Change Agriculture and Food SecurityIFPRI-PIM
This poster was presented by Sophia Huyer (CCAFS / CIAT) for the pre-Annual Scientific Conference meeting organized for the CGIAR research program gender research coordinators on 4 December.
The annual scientific conference of the CGIAR collaborative platform for gender research took place on 5-6 December 2017 in Amsterdam, the Netherlands, where the Platform is hosted (by KIT Royal Tropical Institute).
Read more: http://gender.cgiar.org/gender_events/annual-scientific-conference-capacity-development-workshop-cgiar-collaborative-platform-gender-research/
Role of Social Media in Oral and Maxillofacial SurgerySapna Vadera
The document discusses the role of social media in oral and maxillofacial surgery. It begins by introducing social media and its impact on how doctors and patients interact. It then provides statistics on social media usage among the general public and medical professionals. The main roles and uses of social media for patients and surgeons are described, such as patients using it to research procedures and surgeons using it for continuing education and professional networking. Potential drawbacks like misinformation and privacy issues are covered. Guidelines for surgeons' appropriate social media use are presented. The conclusion emphasizes that social media is becoming more important for engaging with patients, education, and the future of the field.
This program developed and delivered a computer literacy curriculum for promotores/community health workers along the Arizona-Mexico border to help address breast cancer knowledge gaps. A total of 17 promotores participated in the program, which included an initial assessment of their computer skills and informational needs. Based on the results, a 6-session curriculum was created covering basic computer skills, finding reliable health information online, website evaluation, and using resources to create educational materials for their communities. Post-training evaluations found that the promotores improved their computer skills and felt better prepared to address breast cancer in their work. Future iterations of the program will deliver more content online and utilize social media.
The meeting discussed increasing rates of early-age onset colorectal cancer (EAO CRC) and summarized efforts to address this trend. Major topics included identifying priority risk factors for EAO CRC like diet, antibiotics and obesity during childhood for further study. Participants agreed to explore relationships between these factors and the microbiome, and develop prospective cohort studies to examine incidence and adenoma outcomes. Next steps involve continued collaboration to seek funding and publish findings to inform further research.
- Melva Covington of Sanofi discusses strategies for increasing diversity in clinical trials to better represent populations impacted by medical conditions. Currently, racial and ethnic minorities are underrepresented in trials compared to disease prevalence.
- Covington emphasizes the importance of early and sustained engagement with advocacy groups and communities to build trust and partnerships for recruitment and retention. She also stresses using diverse recruitment strategies and culturally competent materials.
- Efforts are underway across the industry and with groups like the FDA to improve representation and data collection in trials through initiatives like standardizing methods and increasing proportional representation. However, more work remains to modernize clinical trials and ensure underserved populations are meaningfully included.
To demonstrate Participatory Action Research (PAR) used to explore, collect and analyse data to understand children’s information experience including their
perception of cancer and information culture; information needs, information seeking behaviour, barriers and enablers.
The document describes a study that evaluated the effectiveness of a community-based intervention called "Friend to Friend" in encouraging Latin American women to undergo breast cancer screening. The intervention involved educational house parties for 17 Latin American women. Surveys before and after found that attitudes towards mammography improved, and 16 of 17 participants received a mammogram at the 6-month follow up. The study suggests the program successfully targeted individual, community, and environmental factors to promote breast cancer prevention through education and social support networks within the Latin American community.
The document summarizes a qualitative study that explored the lived experiences of 15 breast cancer survivors from diagnosis through treatment and beyond. Three major themes emerged from interviews: 1) coping with the stressful diagnosis and treatment process and adjustments required, with some developing journaling techniques; 2) family support being key to providing strength through treatment; 3) feeling abandoned after treatment ended and uncertainty around what survivorship means. The study provided insight into the experiences of women diagnosed with breast cancer who have completed treatment.
Sociocultural and Health Correlates Related to Colorectal Cancer Screening Ad...Kelly Brittain
This study examined factors that influence colorectal cancer (CRC) screening adherence among urban African Americans. The researchers analyzed data from 129 African American participants to identify correlations between CRC screening and cultural identity, social support, CRC beliefs, informed decision making, and health factors. Key findings included: 1) religiosity and having a primary care provider predicted colonoscopy adherence; 2) collectivism, present-time orientation, and informed decision predicted fecal occult blood testing. The results suggest nurses should consider patients' social support, CRC beliefs, and health concerns when discussing CRC screening.
Participation of the population in decisions about their health and in the pr...Pydesalud
Póster presentado por Lilisbeth Perestelo en el congreso Summer Institute for Informed Patient Choice (SIIPC14) celebrado del 25 al 27 de junio de 2014 en Dartmouth, Hanover (EEUU). Web: http://siipc.org
Contacto: lperperr@gobiernodecanarias.org
This document presents a final report on a multi-pronged public health intervention to raise HIV/AIDS awareness and encourage testing in Florida on World AIDS Day 2014. Three approaches were evaluated: 1) An art installation and candlelight vigil honoring those with HIV/AIDS. 2) A health fair with HIV/STD testing at a university in an African American neighborhood with high HIV rates. 3) A panel discussion and testing at a predominantly African American church in the same neighborhood. The goal was to increase awareness and testing among at-risk groups like African Americans in Florida, who have disproportionately high HIV rates. Evaluation methods included event attendance, media coverage, testing rates, and interviews. The results showed the events raised awareness and some
Digital communications bring opportunity and risk to the therapeutic relationship. Doctors and other health professionals can learn to collaborate in person and online to protect informed decision making. Modified slightly from a talk August 8 2019 at Brigham & Women's Hospital/Dana-Farber Cancer Institute.
This document describes the development of partnerships and recruitment efforts for a prostate cancer education intervention program for African American men and women. A community-academic-clinical team was formed to guide the project. Focus groups were conducted with 81 African American men and women to understand current knowledge and attitudes about prostate cancer screening and research participation. Based on focus group findings, a four-week education program was developed and implemented for 56 of the original focus group participants. The goal was to assess changes in knowledge and attitudes about prostate cancer and research after the education program. Lessons learned from the recruitment strategies could help promote cancer research participation among minority communities.
This study evaluated the acceptability of an oral rinse screening test for head and neck cancer among 150 low-income Black Americans. Participants found the rinse to be highly acceptable and easy to use. They agreed they would repeat the test if prescribed by a doctor and engage in preventative behaviors if results indicated cancer risk. Those employed slightly disliked the taste but were more motivated to follow-up on results. The rinse shows promise as an accessible screening method that could promote early cancer detection in high-risk groups.
Running Head Colorectal Cancer Prevention Program-Evaluation Des.docxaryan532920
The document describes a proposed tobacco health education program that aims to educate the public about the dangers of tobacco use. The 15-day program targets youth and middle-aged individuals, who have high rates of tobacco use. It will use various promotional strategies, including social media, printed brochures, and billboards, to educate at least 3,000 people. The program is based on the 4Ps of social marketing: substituting tobacco with tea (product), increasing tobacco prices by $2 (price), closing designated smoking areas (place), and banning tobacco advertisements (promotion). The goal is to discourage tobacco use and reduce related health issues like cancer. Stakeholders will manage program evaluation to determine if objectives are achieved.
1) The document outlines a prostate cancer screening program called Pro-Screen for African American men over age 40 living in East Tampa, Florida.
2) The primary objective is to increase prostate cancer screening behaviors by 33% by the end of 2012 through education, reducing barriers, and increasing awareness of screening facilities.
3) Key elements of Pro-Screen include increasing knowledge of prostate cancer risks and screening, enhancing self-efficacy to get screened, developing social support networks, and reducing cost and access barriers through a screening fund.
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This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
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This lays foundation of scoping research project what are the
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Scope Definition: Clearly outline the boundaries of the research in terms of geographical focus, target demographics (e.g., age, socio-economic status), and industry sectors (e.g., healthcare IT).
3. Review Existing Literature and Resources
Literature Review: Conduct a thorough review of existing research, market reports, and relevant literature to build foundational knowledge.
Gap Analysis: Identify gaps in existing knowledge or areas where further exploration is needed.
4. Select Research Methodology and Tools
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5. Ethical Considerations and Compliance
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Data Privacy: Implement measures to protect participant confidentiality and adhere to data protection regulations (e.g., GDPR, HIPAA).
6. Budget and Resource Allocation
Resource Planning: Allocate resources including time, budget, and personnel required for each phase of the research.
Contingency Planning: Anticipate and plan for unforeseen challenges or adjustments to the research plan.
7. Develop Research Instruments
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Participant Recruitment: Plan recruitment strategies to reach and engage the intended participant groups effectively.
9. Data Collection and Analysis Plan
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African american women and colorectal cancer research: Why Your Participation Matters
1. African American Women and Colorectal
Cancer Research: Why Your Participation
Matters
KELLY BRITTAIN, PHD, RN
MICHIGAN STATE UNIVERSITY
COLLEGE OF NURSING
2. I will explain:
How a research topic/question is developed
How this works in a research study
How research participants are recruited
What we do with the results
What is done after the study is over
5. Reducing Colorectal Cancer Risks
Colorectal Cancer Screening
Annual:
Fecal Occult Blood Test (gFOBT)
Fecal Immunochemical Test (FIT)
Every 3 years:
FIT-DNA (Colorguard®)
Every 10 years:
Colonoscopy
Colorectal Cancer Risk Factors
6. My Goal
• To make sure that our voice and perspectives are represented in research.
• Develop solutions (interventions) will work for us.
7. My Studies
The Influence of Family and Cultural Identity on Informed Decision- Making
o Developing and Testing a Mobile App to Increase Informed Decisions about
Colorectal Cancer Screening
Colorectal Cancer Awareness for Women via Facebook
African American patients’ intent to screen for colorectal cancer: Do cultural
factors, health literacy, knowledge, age and gender matter?
Sociocultural and Health Correlates Related to Colorectal Cancer Screening
Adherence Among Urban African Americans
Barriers and Facilitators for Adoption of the Mediterranean Diet to Reduce
Colorectal Cancer Risk in African Americans
8. How Research Participants Are Recruited
African American men and women
Age 50 and older
Able to read and write in English
No personal history of colorectal cancer
Have insurance coverage for CRC screening
Recruited from Detroit businesses and peer-to-peer (social network)
Newer methods: ResearchMatch.org (You should sign up!)
9. Results
Dependent on the number of people that participate
Findings:
Difference between African American Men and Women related to cultural
identity
Family matters most
African Americans with Diabetes at most risk for not being screened
Health literacy is important to colorectal cancer screening intention
Women thought the mobile app would be good to facilitate talking to
their provider about colorectal cancer screening
Facebook can be used to keep women engage about colorectal cancer risk
reduction and screening
10. What We Do With the Results
Conferences (Posters & Podiums)
Publications
Community presentations
More research
11. What is done after the study is over
Come up with another question that needs to be answered until Colorectal
Cancer disparities on longer exist
12. Summary
How a research topic/question is developed: Impact on an important health issue &
personal connection/experience
How this works in a research study: My research
How research participants are recruited: Depends on the target population and the
question(s) to be answered. More emphasis on healthy populations or those with chronic
diseases. Join ResearchMatch
What we do with the results: Share (conferences, publications, community, students)
What is done after the study is over: Start over
As a preface to my research, I’m going to tell you a bit about myself. I am a native Detroiter and have had a passion for the community for as long as I can remember. I’ve been a nurse for 17 years, but much of my career, a little over 14 years has been spent in the community with children, adults, families, the insured and uninsured. It was the plight of hospitalized asthmatic children that led me to the community and in a since I’ve never looked back. I’ve been a school nurse, program director working with a community and its leaders to reduce teenage pregnancy and infant mortality through the use of lay workers, developed hospital outreach and education programs on the east side of Detroit using parish nurses, school based clinics, senior programs, community health workers and community based agencies. I’ve worked as a care management coordinator for a program that served Detroit’s un and under insured and I’ve directed education, outreach and support programs for the community and cancer patients at Karmanos Cancer Institute. It is my passion for families, the community and the cancer journey, that inspires my research
The issue at hand is the colorectal cancer disparity among African Americans.
According to the American Cancer Society, incidence rates of colorectal cancer among African Americans are 20% higher than in whites (American Cancer Society, 2008).
Mortality rates of colorectal cancer among African Americans are 45% higher than in whites (American Cancer Society, 2008).
In order to participate in the study, potential participants had to be
An African American man or woman
Age 50 and older
Able to read and write in English
No personal history of colorectal cancer
Have insurance coverage for colorectal cancer screening
Most of the sample was recruited from Detroit businesses and peer-to-peer referrals