Skip to main content
Clinical Trials/NCT04958694
NCT04958694
Completed
N/A

Coping and Emotional Development for Adolescents to Reduce Stress for Adolescents

Ann & Robert H Lurie Children's Hospital of Chicago1 site in 1 country36 target enrollmentFebruary 29, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Adolescent Behavior
Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
Enrollment
36
Locations
1
Primary Endpoint
CEDARS Intervention
Status
Completed
Last Updated
4 months ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
February 29, 2024
End Date
July 28, 2025
Last Updated
4 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nia Heard-Garris

MD, MSc, FAAP

Ann & Robert H Lurie Children's Hospital of Chicago

Eligibility Criteria

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

Outcomes

Primary Outcomes

CEDARS Intervention

Time Frame: 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

Time Frame: 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

Time Frame: 4 weeks

There will be one follow-up survey with participants. The final survey will be 1 month post-intervention survey.

Study Sites (1)

Loading locations...

Similar Trials