Intervention to help children affected by the pandemic and disasters
Pragmatic RCT of a Multi-level Mechanistically Informed Community Intervention to Prevent the Onset of Behavioral Health Symptoms Among Socioeconomically Disadvantaged Pandemic Affected Children
This study is testing a program called Journey of Hope-C19 to see if it can help children from disadvantaged communities cope better and avoid mental health problems after experiencing the COVID-19 pandemic and other disasters.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 800 (estimated) |
| Ages | 8 Years to 14 Years |
| Sex | All |
| Sponsor | University of Illinois at Urbana-Champaign Academic / other |
| Locations | 9 sites (Bradenton, Florida and 8 other locations) |
| Trial ID | NCT05639465 on ClinicalTrials.gov |
What this trial studies
This study focuses on preventing behavioral health symptoms in racial and ethnic minority children who have been impacted by the COVID-19 pandemic and other large-scale disasters. It evaluates the efficacy and implementation of a prevention intervention called Journey of Hope-C19, which is designed to support children living in socioeconomically disadvantaged communities. The intervention aims to enhance coping skills and prosocial behavior while providing social support to mitigate the onset of mental health issues. The study will involve children in grades 3-8 who meet specific criteria and will be conducted in various locations in Florida.
Who should consider this trial
Good fit: Ideal candidates for this study are children in grades 3-8 who have experienced the COVID-19 pandemic and another large-scale disaster, and who show signs of emotional distress.
Not a fit: Children currently receiving treatment for a diagnosed mental health condition may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce the risk of mental health issues among vulnerable children affected by the pandemic and disasters.
How similar studies have performed: Other studies have shown success with similar preventative interventions in post-disaster settings, indicating a promising approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * child experienced the COVID-19 pandemic and an additional large-scale disaster * child score is 5 or above on the Strengths and Difficulties Questionnaire * child is in 3- 8th grade at enrollment * the parent or guardian must complete informed consent and child assent * child must speak English or Spanish. Exclusion Criteria: * child is currently receiving treatment for a diagnosed mental health condition * children who are not able to interact with other students in a group work format, regardless of IEP status
Where this trial is running
Bradenton, Florida and 8 other locations
- Boys and Girls Club of Manatee County — Bradenton, Florida, United States (Recruiting)
- Bay District Schools — Panama City, Florida, United States (Active_not_recruiting)
- R'Club Child Care, Inc. — St. Petersburg, Florida, United States (Recruiting)
- Communities in Schools Palm Beach — West Palm Beach, Florida, United States (Active_not_recruiting)
- Coalition for Compassionate Schools — New Orleans, Louisiana, United States (Active_not_recruiting)
- Communities in Schools Gulf South — New Orleans, Louisiana, United States (Recruiting)
- Dickinson Independent School District — Dickinson, Texas, United States (Recruiting)
- CARE Connections — Houston, Texas, United States (Active_not_recruiting)
- Communities in Schools of Galveston County — La Marque, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Tara Leytham Powell, PhD — University of Illinois Urbana Champaign
- Study coordinator: Tara Leytham Powell, PhD
- Email: tlpowell@illinois.edu
- Phone: 2173000917
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.