NCT05621720

Brief Summary

Hong Kong has notably the longest life expectancy in the world. Ever-increasing demand and challenges are posing to the healthcare, social welfare, and elderly care service system. As a global public health strategy to address the increasing burdens, there is a strong urge for an effective approach to enhance the health and self-care ability among the older adults dwelling in the community. Literature suggested that the effectiveness of community-based self-care management programs is inconclusive. In addition, though the concept of the health-social partnership has been widely promoted to improve primary care, literature addressed that the multiple barriers existed throughout the collaboration. More evidence should be sought in the local context to evaluate the effectiveness of self-care complex interventions program among older adults.

Trial Health

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Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
788

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jun 2022

Typical duration for not_applicable

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 6, 2022

Completed
7 days until next milestone

First Submitted

Initial submission to the registry

June 13, 2022

Completed
5 months until next milestone

First Posted

Study publicly available on registry

November 18, 2022

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2025

Completed
Last Updated

October 17, 2024

Status Verified

October 1, 2024

Enrollment Period

2.7 years

First QC Date

June 13, 2022

Last Update Submit

October 15, 2024

Conditions

Keywords

Community-dwelling older adultsSelf-careHealth and social partnership

Outcome Measures

Primary Outcomes (2)

  • Change in Self-efficacy

    The General Self-Efficacy Scale (GSE), developed based on social cognitive theory, initially consisted of 20 items and was later refined to a 10-item version that has been translated into Chinese. The scale items are rated on a 4-point Likert scale, ranging from 1 (not at all true) to 4 (exactly true). The total score ranges from 10 to 40, with higher scores indicating greater self-efficacy, meaning a stronger belief in one's ability to handle various situations effectively.

    Baseline pre-intervention (T1), at three-month when the interventions are completed (T2), and three-month post-intervention (T3)

  • Change in Instrumental Activities of Daily Living (IADL)

    The instrumental activities of daily living is measured by Lawton Instrumental Activities of Daily Living (IADL) Scale-Chinese version, a four-point scale with 9-items of activities which include use of telephone, transportation, shopping, meal preparation, housework, handyman work, laundry, medication management, and money management. Each item rate trichotomously (1 = unable, 2 = needs assistance, 3 = independent) and sum the night responses. Higher score means a worse IADL.

    Baseline pre-intervention (T1), at three-month when the interventions are completed (T2), and three-month post-intervention (T3)

Secondary Outcomes (10)

  • Change in quality of life

    Baseline pre-intervention (T1), at three-month when the interventions are completed (T2), and three-month post-intervention (T3)

  • Change in self-report of pain

    Baseline pre-intervention (T1), at three-month when the interventions are completed (T2), and three-month post-intervention (T3)

  • Change in depression

    Baseline pre-intervention (T1), at three-month when the interventions are completed (T2), and three-month post-intervention (T3)

  • Change in activity of daily living

    Baseline pre-intervention (T1), at three-month when the interventions are completed (T2), and three-month post-intervention (T3)

  • Change in health service utilization

    Baseline pre-intervention (T1), at three-month when the interventions are completed (T2), and three-month post-intervention (T3)

  • +5 more secondary outcomes

Study Arms (2)

Intervention group

EXPERIMENTAL

Subjects in the intervention group will receive a 3-moth community-based health-social partnership program (C-HSPP) led by a nurse case manager, and supported by social workers and community workers.

Other: Case management

Control group

OTHER

Subjects in the control group will receive usual community services and a monthly social control call from trained community workers.

Other: Social control call and usual are

Interventions

On enrolment, the nurse case manager will perform the initial comprehensive assessment based on the Omaha domains of environment, psychosocial, physiological and health-related behavior. The nurse case manager will execute the intervention scheme of teaching, guidance \& counseling, treatments \& procedure, case management, and/or surveillance, with the mutual goal set with clients to promote health and self-efficacy. Home visits and telephone calls will be employed. The referral network to health and social service will be activated as appropriate.

Intervention group

Subjects in the control group will receive usual community service. in addition, a monthly social control call from trained community workers will be given to rule out the possible social effects of the intervention. These social calls will not be related the participants' health condition nor delivery of any health information.

Control group

Eligibility Criteria

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

You may qualify if:

  • (i) People aged 60 or above
  • (ii) Living within the service areas of respective community centers
  • (iii) Cognitively competent with Hong Kong version of Montreal Cognitive Assessment (HK-MoCA) with score ≥22

You may not qualify if:

  • (i) Not communicable
  • (ii) Not reachable by phone
  • (iii) Not living at home
  • (iv) Bed bound
  • (v) With serious mental illness requiring hospitalization in recent 6 months
  • (vi) Already engaged in similar structured health or social programs
  • (vii) Will not stay in Hong Kong for the current three months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Hong Kong Polytechnic University

Kowloon, Hong Kong

RECRUITING

Related Publications (1)

  • Kwok WYY, Wong FKY, Wong AKC, Bayuo J. Community-Based Health-Social Partnership Programme (C-HSPP) for enhancing self-care management among older adults: protocol for a hybrid effectiveness-implementation trial. BMC Public Health. 2025 May 7;25(1):1678. doi: 10.1186/s12889-025-22846-6.

MeSH Terms

Interventions

Case Management

Intervention Hierarchy (Ancestors)

Patient Care PlanningComprehensive Health CarePatient Care ManagementHealth Services Administration

Study Officials

  • Frances Kam-Yuet Wong

    The Hong Kong Polytechnic University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Wilson Yeung-Yuk Kwok

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
The individual who evaluates the outcome(s) of interest would be blinded from having knowledge of the intervention and control group assignment.
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

June 13, 2022

First Posted

November 18, 2022

Study Start

June 6, 2022

Primary Completion

January 31, 2025

Study Completion

April 30, 2025

Last Updated

October 17, 2024

Record last verified: 2024-10

Data Sharing

IPD Sharing
Will not share

Locations