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mHealth Person-centred Self-care Support for Homebound Older Adults: A Hybrid Effectiveness-implementation Study

T

The Hong Kong Polytechnic University

Status

Enrolling

Conditions

Homebound
Mobile Health
Older Adults
Self-Care
Person-Centred Care

Treatments

Behavioral: PCC-based mHealth-assisted self-care support intervention
Behavioral: Provider-led mHealth-assisted self-care support intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06879457
HSEARS20240718004

Details and patient eligibility

About

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).

Full 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.

Enrollment

130 estimated patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

130 participants in 2 patient groups

Intervention Group
Experimental group
Description:
The intervention group emphasizes shared decision-making, goal-setting, and interdisciplinary support. The NCM will co-develop self-care plans with participants.
Treatment:
Behavioral: PCC-based mHealth-assisted self-care support intervention
Control Group
Active Comparator group
Description:
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).
Treatment:
Behavioral: Provider-led mHealth-assisted self-care support intervention

Trial contacts and locations

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Central trial contact

Prof. Arkers Wong

Data sourced from clinicaltrials.gov

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