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Clinical Trials/NCT06879457
NCT06879457RecruitingNot Applicable

Empowering Homebound Older Adults in Self-care Using a Mobile Health-assisted, Person-centred Care Approach: A Hybrid Effectiveness-implementation Design

The Hong Kong Polytechnic University2 sites in 1 country130 target enrollmentStarted: March 10, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
130
Locations
2
Primary Endpoint
Change in self-efficacy assessed using the Chinese version of the General Self-Efficacy Scale

Study Overview

Brief Summary

The aim of the study is to evaluate the effectiveness and implementation of the mobile health (mHealth)-assisted, person-centred care (PCC) self-care support programme for homebound older adults. The researcher will compare PCC approach to a conventional care provider-led model. Participants (n = 130) will receive the intervention of six bi-weekly WhatsApp video call sessions over three months with nurse case managers (NCMs).

Detailed Description

This hybrid effectiveness-implementation, cluster-randomized controlled trial evaluates a mHealth-assisted, PCC self-care support programme for homebound older adults in Hong Kong. Participants (n = 130) receive six bi-weekly WhatsApp video call sessions with NCMs over three months. The study compares a PCC-based approach with a conventional provider-led model. Effectiveness outcomes include self-efficacy, functional independence, and psychosocial well-being. Implementation is assessed using the RE-AIM framework. Findings will inform scalable, digital health interventions for aging populations, improving functional independence, self-care engagement, and healthcare accessibility for homebound older adults.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
60 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Aged 60 years or older;
  • •Unable to leave home more than twice per week due to physical or functional health problems;
  • •Own and have basic proficiency in using a smartphone;
  • •Speak Cantonese;
  • •Indicate sufficient cognitive ability; and
  • •Be moderately frail or below.

Exclusion Criteria

  • •Unable to hear, see, or communicate effectively;
  • •Be completely bed-bound; or
  • •Reside in an area without stable internet coverage.

Arms & Interventions

Intervention Group

Experimental

The intervention group emphasizes shared decision-making, goal-setting, and interdisciplinary support. The NCM will co-develop self-care plans with participants.

Intervention: PCC-based mHealth-assisted self-care support intervention (Behavioral)

Control Group

Active Comparator

The control group does not include shared decision-making or personalized goal-setting. Self-care plans will be developed solely by the nurse case manager (NCM).

Intervention: Provider-led mHealth-assisted self-care support intervention (Behavioral)

Outcomes

Primary Outcomes

Change in self-efficacy assessed using the Chinese version of the General Self-Efficacy Scale

Time Frame: At baseline, 3 months post-intervention , and 6 months post-intervention.

Unit of Measure: Mean score on self-efficacy.

Change in instrumental activities of daily living assessed using the Chinese version of the Lawton Instrumental Activities of Daily Living Scale

Time Frame: At baseline, 3 months post-intervention , and 6 months post-intervention.

Unit of Measure: Mean score on instrumental activities of daily living.

Secondary Outcomes

  • Change in psychological distress assessed using the Chinese version of 21-item Depression Anxiety Stress Scale(At baseline, 3 months post-intervention , and 6 months post-intervention.)
  • Change in quality of life assessed using the Chinese version of the 12-item Short Form Health Survey version 2(At baseline, 3 months post-intervention , and 6 months post-intervention.)
  • Change in perceived loneliness assessed using the Chinese version of the UCLA 3-item Loneliness Scale(At baseline, 3 months post-intervention , and 6 months post-intervention.)
  • Change in functional mobility assessed using the Timed Up and Go Test(At baseline, 3 months post-intervention , and 6 months post-intervention.)
  • Change in sedentary behaviour assessed using the Chinese version of the Sedentary Behaviour Questionnaire for Elderly(At baseline, 3 months post-intervention , and 6 months post-intervention.)
  • Change in frequency of healthcare utilization assessed using the self-reported healthcare utilization survey(At baseline, 3 months post-intervention , and 6 months post-intervention.)
  • Participant reach and recruitment success measured by recruitment records(At baseline.)
  • Participant satisfaction with the intervention assessed using the Chinese version of four-dimension Client Satisfaction Questionnaire(At 3 months post-intervention and 6 months post-intervention.)
  • Service provider acceptability and adoption of person-centred care approach measured by focus group interview(At 3 months post-intervention.)
  • Implementation fidelity and adherence to person-centred care principles measured by session recordings and fidelity checklist(Ongoing monitoring during intervention.)
  • Long-term maintenance and retention of participants measured by cost-effectiveness analysis and retention and dropout records(At 6 months post-intervention.)
  • Barriers and Facilitators to the intervention measured by focus group interview(At 3 months post-intervention.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Arkers, Wong

Associate Professor

The Hong Kong Polytechnic University

Study Sites (2)

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