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

Ann & Robert H Lurie Children's Hospital of Chicago36 enrolled

Overview

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.

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 Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Interventions

CEDARSBEHAVIORAL

This intervention is intended to help adolescents cope with stress and improve positive affect.

Eligibility

Sex: ALLMin age: 14 YearsMax age: 19 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (1)

Ann & Robert H. Lurie Children's Hospital of Chicago

Chicago, Illinois, United States

Outcomes

Primary Outcomes

CEDARS Intervention

Participants will directly benefit from taking part in the interventions by learning and putting into practice new tools to reduce and manage their stress.

Time frame: 8 Weeks

Baseline, Midpoint, and Post-Intervention Surveys

Participants will complete a baseline survey, a mid-point survey, and a post-intervention survey (after the completion of the last CEDARS online module).

Time frame: 8 weeks

Post-Intervention Follow-Up

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

Time frame: 4 weeks

Data from ClinicalTrials.gov

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