Actively Recruiting
Sound Bite-- a Therapeutic Song-writing Program
Led by City University of Hong Kong · Updated on 2026-04-22
120
Participants Needed
1
Research Sites
67 weeks
Total Duration
On this page
Sponsors
C
City University of Hong Kong
Lead Sponsor
T
The Salvation Army, Hong Kong and Macau Command
Collaborating Sponsor
AI-Summary
What this Trial Is About
The research aims to investigate the effectiveness of the therapeutic song-writing program on young people with depressive symptoms. This study adopts a multicentre randomized control trial two arms research design. A randomised controlled trial will compare a typical 7-session therapeutic song-writing program with a waitlist-control group to determine whether the 7-session therapeutic song-writing program can produce better outcomes for young people with depressive symptoms, including improvement in depressive symptoms, self-stigma, self-esteem, sense of hope and social support at post-intervention. The 7-session therapeutic song-writing program will be delivered by trained and experienced social workers and helping professionals who are familiar with music therapy. A research staff, who does not involve in the group allocation and delivery of group intervention, conduct the intervention outcomes assessment of the participants before and after the intervention. Standardized assessment tools are used to assess the intervention outcomes. The ethical considerations of this study were reviewed and approved by the Human and Artefacts Ethics Sub-Committee of the City University of Hong Kong in 2025.
CONDITIONS
Official Title
Sound Bite-- a Therapeutic Song-writing Program
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged between 13 to 24 years
- Have mild to moderate depression and/or anxiety as measured by the Chinese Depression Anxiety Stress Scale-Youth (DASS-Y) with a depression score between 5 and 12
- Be a service user of The Salvation Army social service unit
- Provide informed consent to participate in the study; for those under 18, parental consent is required
You will not qualify if you...
- Have severe depression with a DASS-Y depression score of 13 or higher
- Have severe anxiety with a DASS-Y anxiety score of 8 or higher
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
City University of Hong Kong
Kowloon Tong, Hong Kong, Hong Kong
Actively Recruiting
Research Team
K
Kim-wan Daniel Young, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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