| Registry | NCT06979479, acronym AFL |
|---|---|
| Status | Active not recruiting |
| Study type | Observational |
| Enrollment | 1102 (Actual) |
| Sponsor | Children's Hospital Medical Center, Cincinnati (Other) |
| Conditions | Depression Disorders, Suicidality |
| Interventions | school-based intervention (Behavioral) |
| Dates | start 2021-11-11, primary completion 2025-01-01, completion 2025-06-01 (estimated), first posted 2025-05-20, last updated 2025-05-20 |
| Locations | 1 site in United States |
Related Papers Related Patents Related Grants Related Experts
All trials for Depression Disorders All trials for Suicidality All trials of school-based intervention
Adapt for Life is a mental health and wellbeing program designed to help young people develop healthy behaviors and important life skills to manage stress and mental health challenges. The program is a collaboration between Adapt for Life and Cincinnati Children's Hospital Medical Center.
Purpose of the Study: The primary purpose of the Adapt for Life study is to evaluate the effectiveness of the ADAPT framework in improving mental health outcomes for students. The framework includes steps such as Ask, Describe, Assess, Plan, and Talk, which are designed to help students tackle stress during everyday moments or in times of crisis.
Question the Study is Trying to Answer: The study seeks to answer whether the ADAPT framework can significantly improve students' ability to manage stress, recognize mental health issues, and seek appropriate help. It aims to determine if the program can reduce instances of harmful behaviors and improve overall mental wellbeing among participants.
Purpose: The Adapt for Life study aims to evaluate the effectiveness of the ADAPT framework in improving mental health outcomes for students. The framework includes steps such as Ask, Describe, Assess, Plan, and Talk, which are designed to help students manage stress during everyday moments or in times of crisis.
Study Design: This study is a randomized controlled trial involving students from various schools in the Greater Cincinnati Tri-State area. Participants are randomly assigned to either the intervention group, which receives the ADAPT framework training, or the control group, which receives standard mental health education.
Intervention: The ADAPT framework consists of the following components:
Ask: Encouraging students to ask questions and seek help when needed. Describe: Helping students describe their feelings and experiences accurately. Assess: Teaching students to assess their mental health and stress levels. Plan: Guiding students in planning healthy coping strategies. Talk: Promoting open conversations about mental health. Hypothesis: The study hypothesizes that students who receive the ADAPT framework training will show significant improvements in their ability to manage stress, recognize mental health issues, and seek appropriate help compared to those who receive standard mental health education.
Outcome Measures: Primary outcomes include changes in students' self-reported stress levels, mental health awareness, and help-seeking behaviors. Secondary outcomes include reductions in harmful behaviors and improvements in overall mental wellbeing.
Data Collection: Data will be collected through REDCap surveys, interviews, and observational assessments conducted at baseline, post-intervention, and 3 month post-intervention stages.
Analysis: Statistical analyses will be performed to compare the outcomes between the intervention and control groups. Mixed-methods approaches will be used to assess the qualitative and quantitative aspects of the intervention's effectiveness.
Ethical Considerations: The study will adhere to ethical guidelines for research involving human subjects. Informed consent will be obtained from all participants and their guardians. Confidentiality and privacy will be maintained throughout the study.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Control | These participants took all three surveys before receiving the AFL 4-day course. They instead, were given the AFL 4-day course the following semester. | ||
| Experimental | Behavioral: school-based intervention | These participants took the baseline survey prior to the AFL 4-day course. They then participated in the AFL 4-day course. Immideately after, they took the post-test survey and a 3 month follow up test, 3 months post. |
Sex: All, accepts healthy volunteers
Inclusion Criteria: * Student in 8th-12th grade Exclusion Criteria: * Non-English Speaking
| Facility | City | Country | Status |
|---|---|---|---|
| Cincinnati Children's Hospital Medical Center | Cincinnati, Ohio | United States |