Narrative Therapy Among Young People With Moderate Level of Mental Distress in Hong Kong
A Cluster Randomized Controlled Trial of Narrative Therapy Among Young People With Moderate Level of Mental Distress in Hong Kong
1 other identifier
interventional
770
1 country
1
Brief Summary
This cluster randomized controlled trial (cRCT) aims to evaluate the effectiveness of a narrative therapy (NT) intervention in (i) reducing mental distress, depressive symptoms, and anxiety, as well as (ii) enhancing perceived control and fostering a stronger sense of self among at-risk youth in Hong Kong. Participants are youths with moderate mental health concerns, indicated by K6 scores ranging from 11 to 14. The study involves seven clusters, each based on community hubs, which will be randomly assigned to either the intervention group or a wait-list control group. Clusters assigned to the intervention group will receive six face-to-face sessions led by trained youth workers. Control clusters will receive the same intervention after the initial follow-up period. Participants will be evaluated at baseline, post-intervention, and one-month follow-up. An interim analysis is built for the sake of evaluation of the collected data from the ongoing trial, in which the primary research question is addressed, and which has the potential for modifying the conduct of the study. Furthermore, a qualitative follow-up will be conducted after the trial, involving both participants and the workers delivering the NT intervention. This qualitative component aims to gather feedback on participants' experiences, and inform potential revisions to enhance future implementation. It is hypothesized that youths receiving the NT intervention will show significantly greater improvements in perceived control and sense of self, along with reductions in mental distress, as well as depressive and anxiety symptoms, compared to those in the wait-list control group.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Dec 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 27, 2025
CompletedFirst Posted
Study publicly available on registry
November 17, 2025
CompletedStudy Start
First participant enrolled
December 3, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 31, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 31, 2027
March 30, 2026
August 1, 2025
1.2 years
August 27, 2025
March 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Psychological Distress
The 6-item Kessler Psychological Distress Scale (scores range from 0 to 24 where a higher score indicates a worse outcome)
Baseline, 6-week, and 10-week
Depression and anxiety Symptoms
Depression Anxiety Stress Scales (scores range from 0 to 63 where a higher score indicates more severe symptoms)
Baseline, 6-week, and 10-week
Perceived Control / Self-efficacy
Sense of Mastery Scale (scores range from 7 to 28 where a higher score indicates a a better outcome)
Baseline, 6-week, and 10-week
Secondary Outcomes (8)
Narrative Identity
Baseline, 6-week, and 10-week
Perceived Social Support
Baseline, 6-week, and 10-week
Loneliness
Baseline, 6-week, and 10-week
Resilience
Baseline, 6-week, and 10-week
Rumination
Baseline, 6-week, and 10-week
- +3 more secondary outcomes
Study Arms (2)
NT Intervention
ACTIVE COMPARATORThis narrative therapy intervention will: (i) facilitate shared experiences among participants, (ii) support the reconstruction of personal identity, (iii) promote collective wisdom-sharing and skill development; and (iv) foster solidarity in imagining diverse life possibilities. This approach empowers young people to critically engage with dominant narratives and discover their own authentic paths. The NT intervention consists of six sessions, conducted in a small-group format (6 - 8 participants per group). Youths at similar life stages, such as secondary students, university students, and early-career young professionals, will be grouped together to encourage meaningful discussions and shared experiences. The program consists of six sessions, with the first five lasting 1.5 hours each, and the final session (Section 6) extending to 2 hours for a comprehensive closing. All sessions will be conducted face-to-face by frontline social or youth workers who have received prior training,
Waitlist Control
NO INTERVENTIONParticipants allocated to the waitlist control group will wait for 10 weeks (6 + 4 weeks) before receiving the NT intervention
Interventions
In Hong Kong, deeply ingrained norms and expectations shape each stage of life. As young people navigate their growth, they are constantly influenced by mainstream narratives stemming from sociocultural traditions, family, educators, peers, or social media. These narratives often define socially approved notions of "good" versus "bad," "meaningful" versus "meaningless," and "successful" versus "failing." Many youths may not fully realize how these dominant discourses subtly influence their life choices, often leading them to unconsciously accept predetermined paths they believe they "should" follow. Whether they conform successfully or struggle with these expectations, young people frequently experience pressure and negative emotions. Even more concerning, some internalize these societal judgments, resulting in negative self-perceptions. Through this group program utilizing narrative intervention methods, we aim to provide a safe, supportive space for youth to re-examine and explore th
Eligibility Criteria
You may qualify if:
- JC LevelMind @ Community users at risk for mental distress (Tier 2), with K6 scores ranging from 11 to 14
- Aged between 12 and 24 years
- Sufficiently proficient in Chinese to comprehend verbal instructions
- Able to provide written informed consent (parental consent for participant aged 12-17)
You may not qualify if:
- Known diagnosis of intellectual disability
- Organic brain disorder
- Established psychiatric diagnosis
- Current substance abuse
- Receiving other structured psychological therapies such as module-based psychological therapy, mentalization-based therapy, low-intensity online interventions, cognitive-behavioral therapy, cognitive-behavioral therapy for insomnia, mindfulness, or art-informed therapy within the hub setting or any others outside the hub setting
- Presence of current or active suicidal ideation or attempts
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- The University of Hong Konglead
- Hong Kong Christian Servicecollaborator
- Chinese YMCA of Hong Kongcollaborator
- The Hong Kong Jockey Club Charities Trustcollaborator
- The Boys' and Girls' Clubs Association of Hong Kongcollaborator
- Caritas Medical Centre, Hong Kongcollaborator
- Neighbourhood Advice-Action Councilcollaborator
- St. James' Settlementcollaborator
- Tung Wah Group of Hospitalscollaborator
- Hong Kong Young Women's Christian Associationcollaborator
- Yan Oi Tongcollaborator
- The Salvation Army, Hong Kong and Macau Commandcollaborator
- Hong Kong Playground Association (HKPA)collaborator
- Hong Kong Sheng Kung Hui Welfare Council Limitedcollaborator
- Hong Kong Children and Youth Services (HKCYS)collaborator
- Hong Kong Federation of Youth's Group (HKFYG)collaborator
Study Sites (1)
University of Hong Kong
Hong Kong, Hong Kong
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Christy Lai Ming Hui, PhD
The University of Hong Kong
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
August 27, 2025
First Posted
November 17, 2025
Study Start
December 3, 2025
Primary Completion (Estimated)
January 31, 2027
Study Completion (Estimated)
August 31, 2027
Last Updated
March 30, 2026
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share