RECRUITING

Strengthening Community Mental Health

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Reducing Disparities in Disaster-Related Mental Health Burden: Adaptation of a Multi-level Intervention to Build Community-based Response Capacity

Quick Facts

Study Start:2023-03-25
Study Completion:2025-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06093737

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Individuals 18 years of age or older who are staff or members of an organization that is part of Together Baton Rouge and who participate in the intervention or are/were involved in the adaptation or implementation of the brief intervention in any capacity
  1. * Persons who are not 18 years of age or older and persons who are not staff or members of an organization that is part of Together Baton Rouge and/or not involved with the intervention

Contacts and Locations

Study Contact

Jennifer L Scott, PhD, LCSW
CONTACT
225-578-0433
jenscott@lsu.edu
Tara L Powell, PhD
CONTACT
217-300-0917
tlpowell@illinois.edu

Principal Investigator

Jennifer L Scott, PhD, LCSW
PRINCIPAL_INVESTIGATOR
Louisiana State University Health Sciences Center in New Orleans

Study Locations (Sites)

Together Baton Rouge
Baton Rouge, Louisiana, 70802
United States

Collaborators and Investigators

Sponsor: Louisiana State University and A&M College

  • Jennifer L Scott, PhD, LCSW, PRINCIPAL_INVESTIGATOR, Louisiana State University Health Sciences Center in New Orleans

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-03-25
Study Completion Date2025-06

Study Record Updates

Study Start Date2023-03-25
Study Completion Date2025-06

Terms related to this study

Keywords Provided by Researchers

  • mental health
  • community-based participatory research
  • emotional wellbeing
  • perceived stress

Additional Relevant MeSH Terms

  • Mental Health
  • Emotional Wellbeing
  • Anxiety
  • Depression
  • Stress
  • Coping
  • Perceived Stress
  • Perceived Social Support