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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06039228
Other study ID # KPF23GWP12
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 1, 2023
Est. completion date August 31, 2024

Study information

Verified date September 2023
Source Chinese University of Hong Kong
Contact Jennifer Tang, PhD
Phone 39433753
Email jymtang@cuhk.edu.hk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date August 31, 2024
Est. primary completion date June 30, 2024
Accepts healthy volunteers No
Gender All
Age group 12 Years to 18 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Acceptance and commitment therapy
Four sessions of group acceptance and commitment therapy, with each session lasting for 1.5 hours.

Locations

Country Name City State
Hong Kong Department of Educational Psychology, The Chinese University of Hong Kong Shatin

Sponsors (1)

Lead Sponsor Collaborator
Chinese University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary Acceptance and Action Questionnaire - II Baseline and 4 weeks
Primary The 14-item Resilience Scale Baseline and 4 weeks
Primary Patient Health Questionnaire - 9 Baseline and 4 weeks
Primary General Anxiety Disorder - 7 Baseline and 4 weeks
Primary Perceived Stress Scale Baseline and 4 weeks
Secondary Satisfaction with Life Scale Baseline and 4 weeks
Secondary Pittsburgh Sleep Quality Index Baseline and 4 weeks
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