- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06039228
School-based Group Acceptance and Commitment Therapy for Adolescents
April 14, 2026 updated by: Jennifer Yee Man Tang, Chinese University of Hong Kong
Thriving Through the Storms: A School-based Mental Health Promotion Program for Building Psychological Flexibility and Resilience
The objective of the investigators' mental health promotion intervention premised on the Acceptance and Commitment Therapy (ACT) framework in secondary school settings aims to enhance young people's psychological flexibility and reduce their emotional distress.
ACT is an evidence-based approach that encourages individuals to act in alignment with their identified values.
The investigator's team will employ an ACT protocol for adolescents developed by Louise Hayes and Joseph Ciarrochi.
The study includes a single-group study design.
The investigator will compare the pre- and post-intervention data to assess the feasibility and potential effectiveness of the group intervention.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
61
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Shatin, Hong Kong
- Department of Educational Psychology, The Chinese University of Hong Kong
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
Eligible participants are adolescents who reported mild to moderate severity of psychological distress, including those who report:
- a score of 5-19 on the Patient Health Questionnaire (PHQ-9), or
- a score of 5-14 on the General Anxiety Disorder-7, or
- a score ≥14 on the Perceived Stress Scale.
Exclusion Criteria:
Adolescents will be excluded if they exhibit or report:
- violent or aggressive behavior, or
- active self-injurious or suicidal thought, or
- active psychotic symptom.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group
|
Four sessions of group acceptance and commitment therapy, with each session lasting for 1.5 hours.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Acceptance and Action Questionnaire - II
Time Frame: Baseline and 4 weeks
|
Baseline and 4 weeks
|
|
The 14-item Resilience Scale
Time Frame: Baseline and 4 weeks
|
Baseline and 4 weeks
|
|
Patient Health Questionnaire - 9
Time Frame: Baseline and 4 weeks
|
Baseline and 4 weeks
|
|
General Anxiety Disorder - 7
Time Frame: Baseline and 4 weeks
|
Baseline and 4 weeks
|
|
Perceived Stress Scale
Time Frame: Baseline and 4 weeks
|
Baseline and 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Satisfaction with Life Scale
Time Frame: Baseline and 4 weeks
|
Baseline and 4 weeks
|
|
Pittsburgh Sleep Quality Index
Time Frame: Baseline and 4 weeks
|
Baseline and 4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2023
Primary Completion (Actual)
June 30, 2024
Study Completion (Actual)
August 31, 2024
Study Registration Dates
First Submitted
September 9, 2023
First Submitted That Met QC Criteria
September 9, 2023
First Posted (Actual)
September 15, 2023
Study Record Updates
Last Update Posted (Actual)
April 17, 2026
Last Update Submitted That Met QC Criteria
April 14, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KPF23GWP12
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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