NCT07371988

Brief Summary

The research aims to investigate the efficacy of a narrative therapy group in reducing depressive symptoms among older people. This study adopts a mixed methods research design, involving both quantitative and qualitative approaches. In the quantitative study, a randomised controlled trial will compare a narrative therapy group with a waitlist control group to determine whether an eight-session narrative therapy group can reduce depressive symptoms in older people. The eight-session narrative therapy group will be delivered by a trained and experienced social worker or counsellor, and intervention outcomes will be assessed before and after the intervention using a standardised assessment tool for depressive symptoms. The qualitative study aims to examine the benefits, advantages, and limitations of the narrative therapy group from the users' perspective.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
110

participants targeted

Target at P50-P75 for not_applicable depression

Timeline
4mo left

Started Nov 2025

Shorter than P25 for not_applicable depression

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress61%
Nov 2025Aug 2026

Study Start

First participant enrolled

November 10, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 20, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 28, 2026

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2026

Last Updated

April 24, 2026

Status Verified

February 1, 2026

Enrollment Period

10 months

First QC Date

January 20, 2026

Last Update Submit

April 21, 2026

Conditions

Keywords

Randomized controlled trialDepressive DisordersNarrative Therapy groupSelf-stigmaHopeWellbeing

Outcome Measures

Primary Outcomes (1)

  • Chinese Beck Depression Inventory-II (BDI)

    BDI is a 21-item scale with excellent validity, and reliability (Cronbach's α = 0.91), used to assess self-reported depression. The severity scale is as follows: a score of 0-13 represents minimal or no depression; 14-19 indicates mild depression; 20-28 indicates moderate depression; and 29-63 indicates severe depression. A cut-off point of a BDI score ≥ 14 was adopted in this study as indicative of clinical depression. Each item (e.g. Past failure) is rated on a 4-point scale with scores ranging from "0" to "3". The scores are summed over the items, with higher scores indicating a higher severity of symptoms

    Before and after the 8-week intervention

Secondary Outcomes (4)

  • Chinese Internalised Stigma of Mental Illness (ISMI)

    Before and after the 8-weeks intervention.

  • Chinese Rosenberg Self-Esteem Scale (RSES)

    Before and after the 8-weeks intervention

  • The Chinese Dispositional Hope Scale (DHS)

    Before and after the 8-weeks intervention

  • The Chinese WHO 5-item Well-Being Index (WHO-5)

    Before and after the 8-weeks intervention

Study Arms (2)

8-session narrative therapy group

ACTIVE COMPARATOR

This study includes a two arms parallel groups for comparison. Participants in the intervention group will receive an eight-session narrative therapy group in addition to treatment as usual provided by the elderly centres such as interest classes and recreational activities. The narrative therapy group will be conducted by an experienced and trained social worker and counselor.

Behavioral: Narrative therapy group

Waitlist Control

OTHER

Waitlist control group will receive will receive treatment as usual provided by the elderly centre, including recreational activities and interest classes, at the initial stage and will receive a brief narrative therapy program at a later stage

Other: Treatment as usual (TAU)

Interventions

Narrative therapy group consists of 8 sessions, with one session will be conducted per week, with each session lasting for about 90 minutes. A social worker and a counsellor will be recruited to run narrative groups at collaborative elderly centres. The narrative therapy group provides the following intervention strategies: engagement, de-construction, re-construction, and co-construction of personal identities. A standardized program manual of this narrative group will be developed by the research team. The social workers delivering the narrative therapy group in this project will receive the program manuals, training and supervision from the project team and an experienced clinical psychologist to ensure that the intervention groups follow the program manual.

8-session narrative therapy group

Waitlist control group will receive will receive treatment as usual provided by the elderly centre, including recreational activities and interest classes, at the initial stage and will receive a brief narrative therapy program at a later stage

Waitlist Control

Eligibility Criteria

Age60 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • aged 60 years or above;
  • exhibiting depressive symptoms as assessed using a standardised assessment tool, namely the Chinese Beck Depression Inventory-II (BDI; Byrne et al., 2004), with a BDI score between 10 and 30;
  • being a service user of an elderly centre; and
  • providing informed consent to participate in this research.

You may not qualify if:

  • Individuals with severe depression (i.e. a BDI score ≥ 31), dementia, psychosis, or self-reported suicidal thoughts are excluded from this study; and
  • Individuals currently receiving a therapeutic intervention are not excluded from this study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

City University of Hong Kong

Kowloon Tong, Hong Kong, Hong Kong

RECRUITING

Related Publications (9)

  • Cohen, J. (1988). Statistical power analysis for the behavioral sciences (2nd ed.). Lawrence Erlbaum Associates

    BACKGROUND
  • Lee SW, Stewart SM, Byrne BM, Wong JP, Ho SY, Lee PW, Lam TH. Factor structure of the Center for Epidemiological Studies Depression Scale in Hong Kong adolescents. J Pers Assess. 2008 Mar;90(2):175-84. doi: 10.1080/00223890701845385.

    PMID: 18444112BACKGROUND
  • Madigan, S. (2019). Narrative Therapy (2nd edition). American Psychological Association

    BACKGROUND
  • White, M. (2007). Maps of Narrative Practice. W. W. Norton & Company

    BACKGROUND
  • Young, D. K. W., Ng, P. Y., Pan, J. Y., & Cheng, D. (2017b). Validity and reliability of internalized stigma of mental illness (Cantonese). Research on Social Work Practice, 27(1), 103-110. https://doi.org/10.1177/1049731515576209

    BACKGROUND
  • Sun, Q., Ng, K.-M., & Wang, C. (2012). A validation study on a new Chinese version of the Dispositional Hope Scale. Measurement and Evaluation in Counseling and Development, 45(2), 133-148. https://doi.org/10.1177/0748175611429011

    BACKGROUND
  • Peng W, Zhou Y, Chu J, Liu Z, Zheng K, Yao S, Yi J. Factorial and Criterion Validities of the Chinese Version of Rosenberg Self-Esteem Scale Among Undergraduate Students. Psychol Res Behav Manag. 2024 Dec 5;17:4135-4144. doi: 10.2147/PRBM.S494452. eCollection 2024.

    PMID: 39654814BACKGROUND
  • Lamarca M, Espinosa V, Acuna V, Vila-Badia R, Balsells-Mejia S, Moritz S, Berna F, Konig C, Gaweda L, Group P, Barajas A, Ochoa S. Reducing self-stigma in psychosis: A systematic review and meta-analysis of psychological interventions. Psychiatry Res. 2024 Dec;342:116262. doi: 10.1016/j.psychres.2024.116262. Epub 2024 Nov 16.

    PMID: 39549598BACKGROUND
  • Fung SF, Kong CYW, Liu YM, Huang Q, Xiong Z, Jiang Z, Zhu F, Chen Z, Sun K, Zhao H, Yu P. Validity and Psychometric Evaluation of the Chinese Version of the 5-Item WHO Well-Being Index. Front Public Health. 2022 Mar 30;10:872436. doi: 10.3389/fpubh.2022.872436. eCollection 2022.

    PMID: 35433612BACKGROUND

MeSH Terms

Conditions

DepressionDepressive Disorder

Interventions

Therapeutics

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorMood DisordersMental Disorders

Study Officials

  • Kim-wan Daniel Young, PhD

    City University of Hong Kong

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Kim-wan Daniel Young, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Masking Details
A research assistant, who is not involve in the randomized allocation of participants and delivery of intervention group, will conduct pre- and post-intervention outcome assessments using standardised assessment tools.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants in the intervention group will receive an narrative therapy group in addition to treatment as usual provided by the elderly centre such as interest classes and recreational activities. Narrative therapy group consists 8 session, with one session will be conducted per week, with each session lasting for about 90 minutes. A social worker and a counsellor will be recruited to run narrative groups at collaborative elderly centres. The narrative therapy group provides the following intervention strategies: engagement, de-construction, re-construction, and co-construction of personal identities. Standardized program manual of this narrative group will be developed by the research team. The social workers delivering the narrative therapy group in this project will receive the program manuals, training and supervision from the project team and an experienced clinical psychologist to ensure that the intervention groups follow the program manual.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

January 20, 2026

First Posted

January 28, 2026

Study Start

November 10, 2025

Primary Completion (Estimated)

August 31, 2026

Study Completion (Estimated)

August 31, 2026

Last Updated

April 24, 2026

Record last verified: 2026-02

Locations