Collaborative Stepped Care and Peer Support Programme for Older People At-Risk of or With Depression (JCJoyAge)

May 17, 2022 updated by: Professor Terry Y.S. Lum, The University of Hong Kong

Jockey Club JoyAge: Holistic Support Project for Elderly Mental Wellness

To develop a viable and sustainable best practice model to promote elderly mental wellness and prevent elderly depression for Hong Kong, the Hong Kong Jockey Club Charities Trust has initiated a pilot holistic support project entitled "JC JoyAge: Holistic Support Project for Elderly Mental Wellness". Commenced in October 2016, this 3-year project will deliver six programmes: (1) social services staff training; (2) peer supporters certificate training; (3) outreach and engagement activities for at-risk older adults; (4) standardized prevention and early intervention service; (5) community education programmes; and (6) public awareness and public education activities in four pilot districts in Hong Kong, namely Kwun Tong, Sham Shui Po, Kwai Chung, and Tseung Kwan O. The project aims specifically to:

  1. Evaluate the effectiveness of a collaborative stepped care and peer support programme in engaging older people at-risk of or with depression;
  2. Evaluate the efficacy of the programme in reducing symptoms/risks and promoting wellbeing in older people at-risk of or with depression;
  3. Investigate the impact of the programme on care resources utilization in these older adults.

Study Overview

Detailed Description

Elderly depression is a neglected problem affecting our entire society with grave consequences and high societal costs. Early intervention and prevention can be effective in addressing the problem. The challenges in implementing early intervention and prevention within the existing service platforms, however, are threefold: (1) fragmented services; (2) reactive services; and (3) stigma and low awareness. These challenges resulted in the current service overload and mismatch, which will be compounded by rapid population ageing and mental health workforce shrinkage. The study can address these challenges by (1) realigning existing mental health and elderly services; (2) productive ageing for outreach and engagement; and (3) building up capacity of a preventive network in the neighbourhood. This pilot project therefore combines models of collaborative stepped care and productive ageing, with systematic education programmes, to empower the neighbourhood in providing effective early intervention and prevention for elderly depression. In the four representative pilot districts of Kwun Tong, Sham Shui Po, Kwai Chung, and Tseung Kwan O, community mental health and elderly services will collaborate to deliver a stepped care service protocol for preventing and detecting elderly depression. In 3 years, this project will deliver six programmes: (1) social services staff training; (2) peer supporters certificate training; (3) outreach and engagement activities for at-risk older adults; (4) standardized prevention and early intervention service; (5) community education programmes; and (6) public awareness and public education activities. This will produce a mature service model tested in one-fifth of the districts in Hong Kong with different demographic and service characteristics; create a strong team of Peer Supporters and Social Workers in Elderly Mental Health with clinical competence in preventing elderly depression and promoting elderly mental wellness; significantly raise public and neighbourhood awareness and care for elderly mental wellness; reach out and serve 2,880 at-risk older adults and 960 depressed older adults; and provide evidence on the social impact of the model for further service rollout.

Study Type

Interventional

Enrollment (Actual)

3702

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Kwai Chung, Hong Kong
        • Hong Kong Sheng Kung Hui Lady MacLehose Centre
      • Kwai Chung, Hong Kong
        • New Life Psychiatric Rehabilitation Association
      • Kwun Tong, Hong Kong
        • Christian Family Service Centre
      • Kwun Tong, Hong Kong
        • The Mental Health Association of Hong Kong
      • Sham Shui Po, Hong Kong
        • Caritas Hong Kong
      • Sham Shui Po, Hong Kong
        • New Life Psychiatric Rehabilitation Association
      • Tseung Kwan O, Hong Kong
        • Christian Family Service Centre
      • Tseung Kwan O, Hong Kong
        • Haven of Hope Christian Service

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

60 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • residing in Kwun Tong, Kwai Chung, Tseung Kwan O, or Sham Shui Po; and
  • have one or more known risk factor(s) for developing depression; and/or
  • have depressive symptoms of mild level or above; and
  • able to give informed consent to participate

Exclusion Criteria:

  • known history of autism, intellectual disability, schizophrenia-spectrum disorder, bipolar disorder, Parkinson's disease, or dementia; and
  • imminent suicidal risk; and
  • difficulty in communication

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: NON_RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Intervention group
The intervention group will receive a collaborative stepped care programme provided by registered social workers and trained peer supporters from elderly or mental health service units (NGOs) according to level of risks, symptom severity, and intervention response. Home visits or other format of contact will be delivered by trained peer supporters employed by NGOs to detect and engage hidden cases.

For "at-risk" group, 4 weeks of "selective prevention" group sessions will be provided at the elderly service level by trained peer supporters with registered social worker supervision, on wellness topics tailored to the person's concern as entry point, packaged with mental health information, followed by a review.

For mild group, 6-8 weeks of indicated prevention with psychoeducation or low-intensity psychotherapy would be provided. For moderate group, 6-8 weeks high-intensity cognitive behavioral therapy (CBT) would be provided. All intervention for depressed elderly would be conducted by registered social workers. The trained peer supporters will be matched to individual older adults to walk them through the process with regular follow-up for 1 year.

OTHER: Control group
The control group will receive treatment as usual, which will be determined by the responsible worker from NGO units.
The control group will receive treatment as usual, which will be determined by the responsible workers from NGO units.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline depression at 12 months
Time Frame: Baseline and 12-month follow-up
Depression will be measured by the Patient Health Questionnaire (PHQ-9). The total score will be used, ranging from 0 to 27. Higher scores indicate higher levels of depressive symptoms.
Baseline and 12-month follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline loneliness at 12 months
Time Frame: Baseline and 12-month follow-up
Loneliness will be measured by the UCLA loneliness scale (UCLA-3). The total score will be used, ranging from 0 to 9. Higher scores indicate greater loneliness.
Baseline and 12-month follow-up
Change from baseline life engagement at 12 months
Time Frame: Baseline and 12-month follow-up
Life engagement will be assessed using the typical day interview - a semi-structured interview asking clients about their typical day activities
Baseline and 12-month follow-up
Change from baseline self-harm risk at 12 months
Time Frame: Baseline and 12-month follow-up
Self-harm risk will be measured by the self-harm risk assessment checklist.
Baseline and 12-month follow-up
Change from baseline anxiety at 12 months
Time Frame: Baseline and 12-month follow-up
Anxiety will be measured by the Generalized Anxiety Disorder scale (GAD-7). The total score will be used, ranging from 0 to 21. Higher scores indicate higher levels of anxiety symptoms.
Baseline and 12-month follow-up
Change from baseline cognitive function at 12 months
Time Frame: Baseline and 12-month follow-up
Cognitive function will be measured by the Hong Kong Montreal Cognitive Assessment 5-Minute Protocol (HK-MoCA 5-Min). The total score will be used, ranging from 0 to 30. Higher scores indicate higher levels of cognitive function.
Baseline and 12-month follow-up
Change from baseline social capital at 12 months
Time Frame: Baseline and 12-month follow-up
Participants will be asked to list out names of people who they would turn to when they feel down, and when they need help for trivial things.
Baseline and 12-month follow-up
Change from baseline health-related quality of life at 12 months
Time Frame: Baseline and 12-month follow-up
Health-related quality of life will be measured by the EuroQoL 5 Dimensions 5 Levels (EQ-5D-5L).
Baseline and 12-month follow-up
Change from baseline service utilization at 12 months
Time Frame: Baseline and 12-month follow-up
Service utilization will be measured by the Client Service Receipt Inventory (CSRI).
Baseline and 12-month follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

October 1, 2017

Primary Completion (ACTUAL)

December 31, 2020

Study Completion (ACTUAL)

April 30, 2022

Study Registration Dates

First Submitted

May 29, 2018

First Submitted That Met QC Criteria

July 10, 2018

First Posted (ACTUAL)

July 20, 2018

Study Record Updates

Last Update Posted (ACTUAL)

May 18, 2022

Last Update Submitted That Met QC Criteria

May 17, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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