Strengthening Community Mental Health
NCT06093737 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300
Last updated 2023-10-23
Summary
The goal of this clinical trial is to examine the impact of the Communities Organizing for Power through Empathy (COPE) intervention in adults in communities having recently experienced or at risk of experiencing disaster. The main questions it aims to answer are:
* How does the COPE intervention affect individual mental health?
* How does the COPE intervention affect protective factors like coping and social support?
* How does the COPE intervention affect community resilience?
* How does delivery of the COPE intervention in partnership with a broad-based organization affect participant recruitment and retention, as well as outcomes?
Participants will participate in the three session COPE intervention. Researchers will compare individuals who participate in the COPE intervention to individuals who participate in house meetings to see if the COPE intervention improves mental health, coping, social support and community resilience. Researchers will also examine factors that affect implementation and intervention delivery.
Conditions
- Mental Health
- Emotional Wellbeing
- Anxiety
- Depression
- Stress
- Coping
- Perceived Stress
- Perceived Social Support
Interventions
- BEHAVIORAL
-
COPE: Communities Organizing for Power through Empathy
A three session brief group psychoeducational intervention. Session 1 is 4 hours, Session 2 and 3 are 1.5 hours. It is delivered in groups of 8-15 people with sessions spaced 1 month apart.
Sponsors & Collaborators
-
National Academies of Sciences, Engineering and Medicine
collaborator UNKNOWN -
University of Illinois at Urbana-Champaign
collaborator OTHER -
Louisiana State University and A&M College
lead OTHER
Principal Investigators
-
Jennifer L Scott, PhD, LCSW · Louisiana State University Health Sciences Center in New Orleans
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-03-25
- Primary Completion
- 2025-06-30
- Completion
- 2025-06-30
Countries
- United States
Study Locations
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