DepresssionPlaybackNCT07548463
Playback Theatre Program for Adolescents and Youth
A study testing Playback theatre program in people with Depresssion, run by City University of Hong Kong at 1 site in Hong Kong.
Trial summary
The research aims to investigate the effectiveness of playback theatre program on improving mental health for adolescents and youth. This study adopts a multicentre randomized control trial two arms research design. Read more about this study
- Who is it for?
- Ages 13 to 24 yearsHealthy volunteers can take part
- Conditions the study is for
- Depresssion
- What is being tested?
- Playback theatre program
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 120 participants
- Where
- 1 siteHong Kong
- Study dates
- 1 Sep 2026to 31 Oct 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 13 to 24 years
- All sexes
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- aged between 13 to 24 years;
- 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;
- service users of The Salvation Army social service unit; and
- giving informed consent to this research work. For those aged below 18, parental consent will be obtained.
Who cannot join
- Having severe depression (i.e. a DASS-Y Depression score ≥ 13);
- Having severe anxiety (i.e. a DASS-Y Anxiety score ≥ 8); and
- Having suicidal risk
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Hong Kong1 site, 1 recruiting
- Recruiting
City University of Hong Kong
Kowloon Tong, Hong Kong
Young Daniel Kim-wan, PhD, +852 34428954 ext. 8954, dkwyoung@cityu.edu.hk
About this study
Official title: Playback Theatre Program on Improving Mental Health for Adolescents and Youth
The research aims to investigate the effectiveness of playback theatre program on improving mental health for adolescents and youth.
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 playback theatre 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 playback theatre 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 2026.
Read the detailed description
Psychosocial interventions have been shown to be effective in improving the mental health of adolescents and youth. Among the different types of psychosocial interventions, playback theatre program has been shown to be effective in improving depression, anxiety and self-esteem. In a typical playback theatre, participants play the roles of a teller, the conductor, the actors and the audience. After a short introduction, the conductor asks the members of the audience to tell a moment or feeling from their lives. After the teller sharing the story, the actors immediately improvise a piece of theatre, in which they reflect back the story with empathy. Playback improvisation can have a powerful effect on the storyteller, the actors and the audience.
Method Aim. The research aims to investigate the effectiveness of playback theatre program on improving mental health for adolescents and youth.
Design. This research study adopts mixed methods research design, involving both quantitative and qualitative study. The quantitative study aims to investigate the effectiveness of the playback theatre program for adolescent and youth people with depressive symptoms. The qualitative study aims to examine the benefits, advantages and limitations of the playback theatre program from the users' perspective. 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 2026.
Quantitative Research Method Objective. This quantitative study aims to investigate the effectiveness of the playback theatre program for adolescents and youth with mental health issues.
Hypotheses: After completing the playback theatre program, participants will show significantly greater improvement in depressive symptoms, anxiety symptoms, self-stigma, self-esteem and sense of hope at post-intervention.
Research Design. This study is a multicentre randomised waiting list control study. Eligible participants will be recruited from local secondary schools and Salvation Army social service centres in different districts, through open recruitment via promotional activities and referrals from these centres. A total of 120 participants will be recruited over a study period of approximately 15 months. Using block randomisation, 120 eligible participants will be randomly allocated in a 1:1 ratio to an intervention group or a waitlist control group. 60 participants in the intervention group will receive a playback theatre program. 60 participants on the waiting list will not receive an intervention in the initial phase, but will receive the same playback theatre program at a later stage. 5 intervention groups and 5 waitlist control groups will be conducted, with each intervention group consisting of 12 participants. A research assistant, blinded to randomised allocation, will conduct pre- and post-intervention outcome assessment using standardised assessment tools. See Figure 1 for the flow of participants through each stage of the study.
Intervention group. The playback theatre program consists 7 session. One session will be conducted per week, with each session lasting for about 90 minutes. A social worker and a helping professional who is familiar with music therapy will be recruited to run the playback theatre program at a collaborative social service centre and school. A standardized program manual is designed by the research team. The social worker and a counsellor who run the playback theatre program will receive training and supervision on conducting the playback theatre program by the research team.
Data analysis. An analysis will be performed in accordance with the intent-to-treat principle using multiple imputation method analysis for any missing data. For all analyses, two-tailed p values of < 0.05 is considered statistically significant. Data analyses will be performed using SPSS 29.0. Within group intervention effects are investigated using pair-sample t-test. Between group intervention effects are investigated using 2 (group) x 2 (time) repeated measures of one-way analysis of variance (ANOVA). Within and between group effect sizes are computed using Cohen's d, with values of 0.2, 0.5, and 0.8 considered as small, medium, and large respectively.
Qualitative Research Method Objective. This qualitative study aims to explore the benefits, advantages and limitations of the playback theatre program from the users' perspective.
Research Design. The qualitative study uses an interpretative interview method with purposive sampling. 5 focus groups will be conducted, with each focus group consisting of 2-4 participants selected from each intervention group.
Data collection. Each focus groups will be facilitated by a research staff with an interview protocol developed for this study. Participants will be asked questions such as the following: "In what ways, if any, did the intervention group help you to improve your mental health such as depression and anxiety"; "In what ways, if any, did the intervention group help you to improve self-esteem and build up a sense of hope?"; "What are the advantages and limitations, if any, of the intervention group?"; "and "Any suggestions, if any, for improving the intervention group?". The results of the qualitative analysis will provide insights for further development and modifications of the playback theatre program.
Data analysis. The content of focus groups will be audio-recorded and transcribed into verbatim by the research team. All transcripts of the focus groups will be coded. These codes will then be reviewed and grouped into broader categories and subcategories, resulting in themes and subthemes.
Reflective thematic analysis will be used to identify, analyse and report themes so that themes can be developed both inductively (i.e. data-driven) and deductively (i.e. theory-driven). The research team will systematically read and re-read the transcripts, following the six stages of analysis, including: (1) becoming familiar with the data, (2) generating codes, (3) constructing themes, (4) reviewing potential themes, (5) defining and naming themes, and (6) producing the report.
- Conditions
- Depresssion
- Being tested
- Playback theatre program, Waitlist control group
- Keywords
- Young people, Depression, Playback theatre, Self-stigma, Hope, Randomized Control Trial
- Medical subject headings
- Depression
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Playback theatre programBehavioural
The playback theatre program consists of 7 sessions. One session will be conducted per week, with each session lasting for about 90 minutes. A social worker and a helping professional who is familiar with music therapy will be recruited to run the playback theatre program at a collaborative social service centre and school. A standardized program manual is designed by the research team. The social worker and a counsellor who run the playback theatre program will receive training and supervision on conducting the playback theatre program by the research team
Waitlist control groupBehavioural
Waitlist control group will receive will receive treatment as usual provided by the collaborative centres and schools, including recreational activities and interest classes, at the initial stage and will receive the same playback theatre program at a later stage
| Study group | Role | What they receive |
|---|---|---|
| Intervention group | Active comparator | Playback theatre program Receives: Behavioral: Playback theatre program |
| Waitlist Control | Other | Waitlist control group will receive will receive treatment as usual provided by the collaborative centres and secondary schools, including recreational activities and interest classes, at the initial stage and will receive the same playback theatre program at a later stage. Receives: Behavioral: Waitlist control group |
What is being measured
The primary outcome is the main question the study is designed to answer.
The Chinese Depression Anxiety Stress Scale (DASS-Y)
The Chinese Depression Anxiety Stress Scale (DASS) DASS is a 21-item scale to assesses participants' self-reported depression, anxiety, and stress with good validity and reliability (Cronbach's α = 0.80 for the DASS Anxiety subscale, 0.83 for the DASS Depression subscale, 0.82 for the DASS Stress subscale, and 0.92 for the DASS total scale). Each item (e.g. I felt down-hearted and blue) is scored from 0 (did not apply to me at all) to 3 (applied to me very much or most of the time). The scores are summed over the items with higher scores indicating a higher severity of symptoms
Measured: It will be used before and after the intervention (over 7-weeks)
Secondary outcomes (4)
The Chinese Internalised Stigma of Mental Illness (ISMI)
The Chinese Internalised Stigma of Mental Illness (ISMI) is a 10 -item self-reported scale to measure changes in self-stigma in four dimensions, i.e. shame/alienation (ISMI-SH), stereotype endorsement (ISMI-SE), perceived discrimination (ISMI-PD) and social withdrawal (IMIS-SW), with good validity and reliability (Cronbach's α = 0.93; 0.85; 0.75; 0.84 and for ISMI total scale, ISMI-SH, ISMI-SE, ISMI-PD, ISMI-SW). Each item (e.g. People discriminate against me because I have a mental illness) is rated with a score on a 4-point scale which ranges from "1" (strongly agree) to "4" (strongly disagree). Scores are averaged over the items with higher scores indicating greater self-stigma
Measured: It will be used before and after the intervention (over 7-weeks)
The Chinese Rosenberg Self-Esteem Scale (RSES)
The Chinese Rosenberg Self-Esteem Scale (RSES) is a 10-item scale to assess participants' self-reported self-esteem in two dimensions, i.e. self-worth (RSES-SW) and self-depreciation (RSES-SD) with good validity and reliability (Cronbach's α = 0.63; 0.74, and 0.81 for RSES, RESE-SW, and RSES-SD). Each item (e.g. I feel that I have a number of good qualities) is rated on a 4-point scale with scores ranging from "1" (strongly agree) to "4" (strongly disagree). The scores are summed over the items with higher scores indicating better self-esteem.
Measured: It will be used before and after the intervention (over 7-weeks)
The Chinese Hope Scale (HOPE)
The Chinese Hope Scale (HOPE) is a 12-item scale to assess participants' self-reported hope in two dimensions, i.e., agency (i.e., goal-directed energy) and pathways (i.e., planning to accomplish goals) with good validity and reliability (Cronbach's α = 0.81; 0.70 and 0.76 for the Hope total scale, agency subscale and pathway subscale). Each item (e.g. I can think of many ways to get out of a jam) is answered using an 8-point scale ranging from "1" (definitely false) to "4" (definitely true). The scores are summed over the items, so that higher scores indicate a higher level of hope.
Measured: It will be used before and after the intervention (over 7-weeks)
The Chinese Multidimensional Scale of Perceived Social Support (MSPSS)
The Chinese Multidimensional Scale of Perceived Social Support (MSPSS) is a 12-item scale to assess participants' self-reported hope in three dimensions, i.e., family, friends, and significant others with good validity and reliability (Cronbach's α = 0.91, 0.77, 0.88, and 0.88 for the MSPSS total scale, family, friends, and significant others subscale). Each item (e.g. There is a special person with whom I can share joys and sorrows) is answered using an 7-point scale ranging from "1" (strongly disagree) to "7" (strongly agree). The scores are summed over the items, so that higher scores indicate greater social support
Measured: It will be used before and after the intervention (over 7-weeks)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Apr 2026
- Study start1 Sep 2026 (estimated)
- Primary completion31 Aug 2027 (estimated)
- Study completion31 Oct 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (8)Papers the sponsor has linked to this study.
- Other trials for DepresssionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- A randomized controlled trial will compare a typical 7-session playback theatre program with a waitlist-control group. Intervention group. The playback theatre program consists of 7 sessions. One session will be conducted per week, with each session lasting for about 90 minutes. A social worker and a helping professional who is familiar with music therapy will be recruited to run the playback theatre program at a collaborative social service centre and school. A standardized program manual is designed by the research team. The social worker and a counsellor who run the playback theatre program will receive training and supervision on conducting the playback theatre program by the research team
- Masking
- Single blind
- Who is masked
- Investigator
- Enrolment
- 120 participants (estimated)
Sponsor and investigators
- Lead sponsor
- City University of Hong Kong
- Sponsor type
- University, hospital or other
- Collaborators
- The Salvation Army, Hong Kong and Macau Command
- Responsible party
- Principal investigator, Daniel Young, City University of Hong Kong
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07548463
- Sponsor's protocol ID
- HU-STA-00002313
- Acronym
- Playback
- Status last verified
- Apr 2026
- First submitted
- 17 Apr 2026
- Last updated
- 9 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Zhou K, Chen J, Huang C, Tang S. Prevalence of and factors influencing depression and anxiety among Chinese adolescents: a protocol for a systematic review. BMJ Open. 2023 Mar 23;13(3):e068119. doi: 10.1136/bmjopen-2022-068119.
PubMed 36958770Wang K, Shi HS, Geng FL, Zou LQ, Tan SP, Wang Y, Neumann DL, Shum DH, Chan RC. Cross-cultural validation of the Depression Anxiety Stress Scale-21 in China. Psychol Assess. 2016 May;28(5):e88-e100. doi: 10.1037/pas0000207. Epub 2015 Nov 30.
PubMed 26619091Munjuluri S, Bolin PK, Amy Lin YT, Garcia NL, Gauna L, Nguyen T, Salas R. A Pilot Study on Playback Theatre as a Therapeutic Aid after Natural Disasters: Brain Connectivity Mechanisms of Effects on Anxiety. Chronic Stress (Thousand Oaks). 2020 Nov 3;4:2470547020966561. doi: 10.1177/2470547020966561. eCollection 2020 Jan-Dec.
PubMed 33210057Lo LLH, Suen YN, Chan SKW, Sum MY, Charlton C, Hui CLM, Lee EHM, Chang WC, Chen EYH. Sociodemographic correlates of public stigma about mental illness: a population study on Hong Kong's Chinese population. BMC Psychiatry. 2021 May 29;21(1):274. doi: 10.1186/s12888-021-03301-3.
PubMed 34051783Li XH, Wong YI, Wu Q, Ran MS, Zhang TM. Chinese College Students' Stigmatization towards People with Mental Illness: Familiarity, Perceived Dangerousness, Fear, and Social Distance. Healthcare (Basel). 2024 Aug 27;12(17):1715. doi: 10.3390/healthcare12171715.
PubMed 39273739Jiang C, Zhu Y, Luo Y, Tan CS, Mastrotheodoros S, Costa P, Chen L, Guo L, Ma H, Meng R. Validation of the Chinese version of the Rosenberg Self-Esteem Scale: evidence from a three-wave longitudinal study. BMC Psychol. 2023 Oct 18;11(1):345. doi: 10.1186/s40359-023-01293-1.
PubMed 37853499Ho SM, Ho JW, Bonanno GA, Chu AT, Chan EM. Hopefulness predicts resilience after hereditary colorectal cancer genetic testing: a prospective outcome trajectories study. BMC Cancer. 2010 Jun 11;10:279. doi: 10.1186/1471-2407-10-279.
PubMed 20537192Duagi D, Carter B, Farrelly M, Lisk S, Shearer J, Byford S, James K, Brown JSL. Long-term effects of psychosocial interventions for adolescents on depression and anxiety: a systematic review and meta-analysis. EClinicalMedicine. 2024 Jan 5;68:102382. doi: 10.1016/j.eclinm.2023.102382. eCollection 2024 Feb.
PubMed 38273890
Study at a glance
From the registry record, last updated by the sponsor on 9 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Playback Theatre Program on Improving Mental Health for Adolescents and Youth
- ClinicalTrials.gov ID
- NCT07548463
- Acronym / sponsor ID
- Playback / HU-STA-00002313
- Conditions
- Depresssion
- Keywords
- Young people, Depression, Playback theatre, Self-stigma, Hope, Randomized Control Trial
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 120 participants (estimated)
- Lead sponsor
- City University of Hong KongUniversity, hospital or other
- Collaborators
- The Salvation Army, Hong Kong and Macau Command
- Study start
- 1 Sep 2026 (estimated)
- Primary completion
- 31 Aug 2027 (estimated)
- Study completion
- 31 Oct 2027 (estimated)
- First posted
- 23 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The research aims to investigate the effectiveness of playback theatre program on improving mental health for adolescents and youth.
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 playback theatre 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 playback theatre 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 2026.
Detailed description
Psychosocial interventions have been shown to be effective in improving the mental health of adolescents and youth. Among the different types of psychosocial interventions, playback theatre program has been shown to be effective in improving depression, anxiety and self-esteem. In a typical playback theatre, participants play the roles of a teller, the conductor, the actors and the audience. After a short introduction, the conductor asks the members of the audience to tell a moment or feeling from their lives. After the teller sharing the story, the actors immediately improvise a piece of theatre, in which they reflect back the story with empathy. Playback improvisation can have a powerful effect on the storyteller, the actors and the audience.
Method Aim. The research aims to investigate the effectiveness of playback theatre program on improving mental health for adolescents and youth.
Design. This research study adopts mixed methods research design, involving both quantitative and qualitative study. The quantitative study aims to investigate the effectiveness of the playback theatre program for adolescent and youth people with depressive symptoms. The qualitative study aims to examine the benefits, advantages and limitations of the playback theatre program from the users' perspective. 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 2026.
Quantitative Research Method Objective. This quantitative study aims to investigate the effectiveness of the playback theatre program for adolescents and youth with mental health issues.
Hypotheses: After completing the playback theatre program, participants will show significantly greater improvement in depressive symptoms, anxiety symptoms, self-stigma, self-esteem and sense of hope at post-intervention.
Research Design. This study is a multicentre randomised waiting list control study. Eligible participants will be recruited from local secondary schools and Salvation Army social service centres in different districts, through open recruitment via promotional activities and referrals from these centres. A total of 120 participants will be recruited over a study period of approximately 15 months. Using block randomisation, 120 eligible participants will be randomly allocated in a 1:1 ratio to an intervention group or a waitlist control group. 60 participants in the intervention group will receive a playback theatre program. 60 participants on the waiting list will not receive an intervention in the initial phase, but will receive the same playback theatre program at a later stage. 5 intervention groups and 5 waitlist control groups will be conducted, with each intervention group consisting of 12 participants. A research assistant, blinded to randomised allocation, will conduct pre- and post-intervention outcome assessment using standardised assessment tools. See Figure 1 for the flow of participants through each stage of the study.
Intervention group. The playback theatre program consists 7 session. One session will be conducted per week, with each session lasting for about 90 minutes. A social worker and a helping professional who is familiar with music therapy will be recruited to run the playback theatre program at a collaborative social service centre and school. A standardized program manual is designed by the research team. The social worker and a counsellor who run the playback theatre program will receive training and supervision on conducting the playback theatre program by the research team.
Data analysis. An analysis will be performed in accordance with the intent-to-treat principle using multiple imputation method analysis for any missing data. For all analyses, two-tailed p values of < 0.05 is considered statistically significant. Data analyses will be performed using SPSS 29.0. Within group intervention effects are investigated using pair-sample t-test. Between group intervention effects are investigated using 2 (group) x 2 (time) repeated measures of one-way analysis of variance (ANOVA). Within and between group effect sizes are computed using Cohen's d, with values of 0.2, 0.5, and 0.8 considered as small, medium, and large respectively.
Qualitative Research Method Objective. This qualitative study aims to explore the benefits, advantages and limitations of the playback theatre program from the users' perspective.
Research Design. The qualitative study uses an interpretative interview method with purposive sampling. 5 focus groups will be conducted, with each focus group consisting of 2-4 participants selected from each intervention group.
Data collection. Each focus groups will be facilitated by a research staff with an interview protocol developed for this study. Participants will be asked questions such as the following: "In what ways, if any, did the intervention group help you to improve your mental health such as depression and anxiety"; "In what ways, if any, did the intervention group help you to improve self-esteem and build up a sense of hope?"; "What are the advantages and limitations, if any, of the intervention group?"; "and "Any suggestions, if any, for improving the intervention group?". The results of the qualitative analysis will provide insights for further development and modifications of the playback theatre program.
Data analysis. The content of focus groups will be audio-recorded and transcribed into verbatim by the research team. All transcripts of the focus groups will be coded. These codes will then be reviewed and grouped into broader categories and subcategories, resulting in themes and subthemes.
Reflective thematic analysis will be used to identify, analyse and report themes so that themes can be developed both inductively (i.e. data-driven) and deductively (i.e. theory-driven). The research team will systematically read and re-read the transcripts, following the six stages of analysis, including: (1) becoming familiar with the data, (2) generating codes, (3) constructing themes, (4) reviewing potential themes, (5) defining and naming themes, and (6) producing the report.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 2
- Model description
- A randomized controlled trial will compare a typical 7-session playback theatre program with a waitlist-control group. Intervention group. The playback theatre program consists of 7 sessions. One session will be conducted per week, with each session lasting for about 90 minutes. A social worker and a helping professional who is familiar with music therapy will be recruited to run the playback theatre program at a collaborative social service centre and school. A standardized program manual is designed by the research team. The social worker and a counsellor who run the playback theatre program will receive training and supervision on conducting the playback theatre program by the research team
| Arm | Type | Receives |
|---|---|---|
| Intervention group | Active comparator | Behavioral: Playback theatre programPlayback theatre program |
| Waitlist Control | Other | Behavioral: Waitlist control groupWaitlist control group will receive will receive treatment as usual provided by the collaborative centres and secondary schools, including recreational activities and interest classes, at the initial stage and will receive the same playback theatre program at a later stage. |
Who may qualify
- Ages
- 13 to 24 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (4 listed)
- aged between 13 to 24 years;
- 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;
- service users of The Salvation Army social service unit; and
- giving informed consent to this research work. For those aged below 18, parental consent will be obtained.
Key exclusion criteria (3 listed)
- Having severe depression (i.e. a DASS-Y Depression score ≥ 13);
- Having severe anxiety (i.e. a DASS-Y Anxiety score ≥ 8); and
- Having suicidal risk
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Playback theatre programThe playback theatre program consists of 7 sessions. One session will be conducted per week, with each session lasting for about 90 minutes. A social worker and a helping professional who is familiar with music therapy will be recruited to run the playback theatre program at a collaborative social service centre and school. A standardized program manual is designed by the research team. The social worker and a counsellor who run the playback theatre program will receive training and supervision on conducting the playback theatre program by the research team | Behavioural | Intervention group |
| Waitlist control groupWaitlist control group will receive will receive treatment as usual provided by the collaborative centres and schools, including recreational activities and interest classes, at the initial stage and will receive the same playback theatre program at a later stage | Behavioural | Waitlist Control |
Primary outcome
The Chinese Depression Anxiety Stress Scale (DASS-Y)
Time frame: It will be used before and after the intervention (over 7-weeks)
The Chinese Depression Anxiety Stress Scale (DASS) DASS is a 21-item scale to assesses participants' self-reported depression, anxiety, and stress with good validity and reliability (Cronbach's α = 0.80 for the DASS Anxiety subscale, 0.83 for the DASS Depression subscale, 0.82 for the DASS Stress subscale, and 0.92 for the DASS total scale). Each item (e.g. I felt down-hearted and blue) is scored from 0 (did not apply to me at all) to 3 (applied to me very much or most of the time). The scores are summed over the items with higher scores indicating a higher severity of symptoms
4 secondary outcomes
The Chinese Internalised Stigma of Mental Illness (ISMI)
Time frame: It will be used before and after the intervention (over 7-weeks)
The Chinese Rosenberg Self-Esteem Scale (RSES)
Time frame: It will be used before and after the intervention (over 7-weeks)
The Chinese Hope Scale (HOPE)
Time frame: It will be used before and after the intervention (over 7-weeks)
The Chinese Multidimensional Scale of Perceived Social Support (MSPSS)
Time frame: It will be used before and after the intervention (over 7-weeks)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Sep 2026.
- Background: PubMed 36958770Zhou K, Chen J, Huang C, Tang S. Prevalence of and factors influencing depression and anxiety among Chinese adolescents: a protocol for a systematic review. BMJ Open. 2023 Mar 23;13(3):e068119. doi: 10.1136/bmjopen-2022-068119.
- Background: PubMed 26619091Wang K, Shi HS, Geng FL, Zou LQ, Tan SP, Wang Y, Neumann DL, Shum DH, Chan RC. Cross-cultural validation of the Depression Anxiety Stress Scale-21 in China. Psychol Assess. 2016 May;28(5):e88-e100. doi: 10.1037/pas0000207. Epub 2015 Nov 30.
- Background: PubMed 33210057Munjuluri S, Bolin PK, Amy Lin YT, Garcia NL, Gauna L, Nguyen T, Salas R. A Pilot Study on Playback Theatre as a Therapeutic Aid after Natural Disasters: Brain Connectivity Mechanisms of Effects on Anxiety. Chronic Stress (Thousand Oaks). 2020 Nov 3;4:2470547020966561. doi: 10.1177/2470547020966561. eCollection 2020 Jan-Dec.
- Background: PubMed 34051783Lo LLH, Suen YN, Chan SKW, Sum MY, Charlton C, Hui CLM, Lee EHM, Chang WC, Chen EYH. Sociodemographic correlates of public stigma about mental illness: a population study on Hong Kong's Chinese population. BMC Psychiatry. 2021 May 29;21(1):274. doi: 10.1186/s12888-021-03301-3.
- Background: PubMed 39273739Li XH, Wong YI, Wu Q, Ran MS, Zhang TM. Chinese College Students' Stigmatization towards People with Mental Illness: Familiarity, Perceived Dangerousness, Fear, and Social Distance. Healthcare (Basel). 2024 Aug 27;12(17):1715. doi: 10.3390/healthcare12171715.
- Background: PubMed 37853499Jiang C, Zhu Y, Luo Y, Tan CS, Mastrotheodoros S, Costa P, Chen L, Guo L, Ma H, Meng R. Validation of the Chinese version of the Rosenberg Self-Esteem Scale: evidence from a three-wave longitudinal study. BMC Psychol. 2023 Oct 18;11(1):345. doi: 10.1186/s40359-023-01293-1.
- Background: PubMed 20537192Ho SM, Ho JW, Bonanno GA, Chu AT, Chan EM. Hopefulness predicts resilience after hereditary colorectal cancer genetic testing: a prospective outcome trajectories study. BMC Cancer. 2010 Jun 11;10:279. doi: 10.1186/1471-2407-10-279.
- Background: PubMed 38273890Duagi D, Carter B, Farrelly M, Lisk S, Shearer J, Byford S, James K, Brown JSL. Long-term effects of psychosocial interventions for adolescents on depression and anxiety: a systematic review and meta-analysis. EClinicalMedicine. 2024 Jan 5;68:102382. doi: 10.1016/j.eclinm.2023.102382. eCollection 2024 Feb.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Playback theatre program in people with Depresssion, run by City University of Hong Kong at 1 site in Hong Kong.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 9 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Kim-wan Daniel Young, PhD (+852 34428954 ext. 8954, dkwyoung@cityu.edu.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The Chinese Depression Anxiety Stress Scale (DASS-Y) (time frame: It will be used before and after the intervention (over 7-weeks)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07548463, which also lists 8 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Sep 2026.