CEDARS Intervention: A Coping, Emotional Development, & Stress Reduction Intervention

Not Applicable

Recruiting

• Conditions: Adolescent Behavior; Stress Reduction; Adverse Childhood Experiences; Positive Attitude

• Registration Number: NCT04958694
• Lead Sponsor: Ann & Robert H Lurie Children's Hospital of Chicago

Brief Summary

Using an adapted stress-reduction intervention called the CEDARS, the investigators will pilot the intervention in adolescents (N=40) to determine the feasibility and acceptability of CEDARS implementation and to investigate adolescent stress reduction. As an exploratory aim, the investigators will explore the influence of the CEDARS on CMH-related behaviors and CMH. The investigators expect that those adolescents who undergo the intervention will have the greatest improvement in mental health symptoms than their waitlisted counterparts. Our secondary hypothesis is that those who report more adversity will also report greater improvement in mental health symptoms than their peers.

Detailed Description

This intervention has been adapted based on feedback from previous focus groups with adolescents, clinical staff, community stakeholders, and a CEDARS workgroup.

Participants will be divided into two groups - 20 in the intervention group and 20 in the waitlisted group.

Adolescents in the intervention group will participate in 7 weekly, 1-hour sessions. This online intervention will feature positive affect and stress reduction skills delivered via self-paced and self-guided modules. The skills are taught through brief didactic and semi-interactive videos followed by invitations and opportunities for practice within the session and at home. Participants will complete a baseline, mid-point, and post-intervention survey to determine the influence of the intervention.

There will be one follow-up survey with participants after the intervention. The survey will take place 1 month after the program has concluded.

Study Timeline

• Study First Submitted: 2021-07-01
• Study First Submitted QC: 2021-07-01
• Study First Posted: 2021-07-12
• Study Start: 2024-02-29
• Status Verified: 2024-10
• Last Update Submitted: 2024-10-28
• Last Update Posted: 2024-10-29
• Primary Completion: 2025-01-31
• Study Completion: 2025-07-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Adolescents ages 14-19
• Adolescents able to speak and understand English fluently
• Adolescents with reliable internet access (for virtual access to online modules)

Exclusion Criteria

• Individuals younger than age 14 and older than age 19
• Individuals who are not able to speak or understand English fluently
• Individuals without reliable internet access

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
CEDARS Intervention	8 Weeks	Participants will directly benefit from taking part in the interventions by learning and putting into practice new tools to reduce and manage their stress.
Baseline, Midpoint, and Post-Intervention Surveys	8 weeks	Participants will complete a baseline survey, a mid-point survey, and a post-intervention survey (after the completion of the last CEDARS online module).
Post-Intervention Follow-Up	4 weeks	There will be one follow-up survey with participants. The final survey will be 1 month post-intervention survey.

Trial Locations

Locations (1)

Ann & Robert H. Lurie Children's Hospital of Chicago; 🇺🇸 Chicago, Illinois, United States