Clinical trial Recruiting at 1 site Interventional Ages 13 to 24

Sound Bite: therapeutic song-writing for young people with depression

Official title: "Everyone is a Hope Builder" Project Study- Therapeutic Song-writing Program

Run by City University of Hong Kong · NCT07371962 · Data updated 2026-11-12

This program will test whether seven sessions of therapeutic song-writing help young people ages 13–24 with mild to moderate depression reduce symptoms and increase hope, self-esteem, and social support.

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Quick facts

Study typeInterventional
Ages13 Years to 24 Years
SexAll
Enrollment120 (estimated)
SponsorCity University of Hong Kong
Academic / other
Locations1 site (Kowloon Tong, Hong Kong)
StatusRecruiting
StartedJuly 17, 2026
Main results expectedAugust 31, 2027
Study endsOctober 31, 2027
Registry record updatedApril 22, 2026
Trial IDNCT07371962 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are 13–24 years old, are service users of The Salvation Army in Hong Kong, and have mild to moderate depression (DASS-Y Depression score 5–12) and consent to participate.

Probably not a fit

Young people with severe depression or anxiety (DASS-Y Depression ≥13 or Anxiety ≥8) are excluded and would not receive benefit from this program, and those who do not engage with group-based or music-based approaches may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This multicentre randomized controlled trial compares a seven-session therapeutic song-writing program (Sound Bite) with a waitlist control in young people who have mild to moderate depressive symptoms. The program is delivered by trained social workers and helping professionals familiar with music therapy, and intervention outcomes are measured before and after by research staff who are not involved in group allocation or delivery. Standardized assessments including the Chinese DASS-Y are used to measure depressive symptoms, self-stigma, self-esteem, sense of hope, and perceived social support at post-intervention. Participants are drawn from service users of The Salvation Army in Hong Kong and must provide informed consent, with parental consent required for those under 18.

Why it matters

Potential benefit: If successful, the program could reduce depressive symptoms and self-stigma while increasing self-esteem, hope, and social support for participating young people.

How similar studies have gone: Therapeutic song-writing and other psychosocial music interventions have shown promising effects on depressive symptoms and social support in previous work, though this specific program's randomized evaluation is novel in this setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. aged between 13 to 24 years;
2. having mild to moderate depression and/or anxiety as assessed using a standardized assessment tool, i.e. Chinese Depression Anxiety Stress Scale-Youth (DASS-Y) with a DASS-Y Depression score between 5 and 12;
3. service users of The Salvation Army social service unit; and
4. giving informed consent to this research work. For those aged below 18, parental consent will be obtained.

Exclusion Criteria:

Those with severe depression (i.e. a DASS-Y Depression score ≥ 13) and/or severe anxiety (i.e. a DASS-Y Anxiety score ≥ 8) are excluded from this study.

Where it's running

  • City University of Hong Kong
    Kowloon Tong, Hong Kong, Hong Kong
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.