Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
NCT07371988

Efficacy of Narrative Therapy for Older People With Depression

Led by City University of Hong Kong · Updated on 2026-04-24

110

Participants Needed

1

Research Sites

42 weeks

Total Duration

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AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Efficacy of Narrative Therapy for Older People With Depression

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 60 years or above
  • Exhibiting depressive symptoms with a Chinese Beck Depression Inventory-II (BDI) score between 10 and 30
  • Being a service user of an elderly centre
  • Providing informed consent to participate in this research
Not Eligible

You will not qualify if you...

  • Having severe depression (BDI score 31 or above), dementia, psychosis, or self-reported suicidal thoughts

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

City University of Hong Kong

Kowloon Tong, Hong Kong, Hong Kong

Actively Recruiting

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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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