Topic
- addiction
- adrenal cancer
- alcohol
- Alzheimer's
- asthma
- biobank
- breast cancer
- cancer
- cessation
- chemotherapy
- colorectal cancer
- diabetes
- disease management
- gastrointestinal illness
- genetics
- health insurance
- hearing loss
- hearing protection
- heart disease
- HIV / AIDS
- HPV
- injury
- liver
- lung cancer
- medical history
- medication adherence
- mental health
- nutrition
- obesity
- oral health
- organ donation
- organ quality
- organ transplant
- other
- ovarian cancer
- physical activity
- post-treatment
- prevention
- prostate cancer
- quality of life
- recurrence
- screening
- skin cancer
- sleep safety
- smoking
- STD
- stroke
- survivorship
- symptoms
- treatment
- vaccination
- weight loss
Audience
- adolescents
- adults
- African Americans
- alumni
- caregivers
- children
- college students
- farmers
- fraternities and sororities
- girls
- health care providers
- high risk
- HMO members
- Latinos
- LGBT
- Medicare enrollees
- men
- mothers
- non-smokers
- older adults
- parents
- patients
- people living with HIV/AIDS
- research volunteers
- school age children
- smokers
- survivors
- transplant recipients
- transplant waiting list
- underserved
- veterans
- women
- young adults
Setting
Technology
Project Overview +
Deliberative Engagement Community in Decisions about Research Spending (DECIDERS) study will develop and evaluate a mechanism to engage communities, particularly minority and underserved communities, in informed deliberations about health research spending priorities.
Aims +
Aim 1. Develop Research CHAT (ReCHAT), a simulation exercise to engage communities in deliberations about health research spending priorities.
Aim 2. Evaluate a deliberative exercise
designed to engage minority and underserved communities in setting research priorities from the perspective of participants.
Aim 3. Describe the health research priorities of Michigan communities, particularly minority and underserved communities.
Aim 4. Return results of statewide ReCHAT sessions to communities, funders, research leaders, and those who participated in interviews or ReCHAT groups.
Aim 5. Assess the impact on participants, communities, research institutions and funders of public involvement in deliberative dialogues about research spending priorities.
Participants +
Steering Committee with members from multiple minority and underserved communities throughout Michigan, and representatives from public health, health professions, and organizations that fund and/or conduct health research. Over 1/2 (optimally 2/3) of the voting members of the Steering Committee will be community members to ensure decisions reflect communities’ preferences and values.
Intervention +
- Options, events and tasks are understandable and meaningful to non-scientists. Unlike the health care version of CHAT, the setting of research priorities, indeed health research itself, is rarely familiar to participants. Materials educate and inform participants about health research and spending priorities. Materials are thoroughly pretested to assure that information is credible and balanced, sufficient but not overwhelming, comprehensible but not oversimplified.
- A wide range of spending options, not limited to those currently considered by funding decision makers, so that communities’ priorities are not constrained by the status quo.
- Options reflect categories of research spending that decision makers find useful and meaningful, so that results from community engagement in priority setting can readily influence decisions.
Keywords
clinic, underserved, health care providers, adults, decision making, community based, software, computer, otherDECIDERS
09/01/2011 - 08/31/2016
Principal Investigator:
Co-Investigator(s):
Eric G. Campbell, PhD
Marion Danis, MD
Kathryn L. Moseley, MD, MPH, FAAP
Zachary Rowe, BBA
Stephanie Solomon, PhD
Victor J. Strecher, PhD, MPH
Matthew Wynia, MD, MPH

