Yan Oi Tong
Hong Kong
Location status: Recruiting
NCT Number: NCT06879457
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).
Interested in participating?
Request Info60 year and older
All sexes
Interventional
Not applicable
Hong Kong
Location status: Recruiting
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants receive six bi-weekly WhatsApp video call sessions with a NCM over three months, using a person-centred care (PCC) approach.
Participants receive six bi-weekly WhatsApp video call sessions with a NCM over three months, based on the conventional provider-led model.
Time frame: At baseline, 3 months post-intervention , and 6 months post-intervention.
Unit of Measure: Mean score on self-efficacy.
Time frame: At baseline, 3 months post-intervention , and 6 months post-intervention.
Unit of Measure: Mean score on instrumental activities of daily living.
Time frame: At baseline, 3 months post-intervention , and 6 months post-intervention.
Unit of Measure: Mean score on quality of life.
Time frame: At baseline, 3 months post-intervention , and 6 months post-intervention.
Unit of Measure: Mean score on psychological distress.
Time frame: At baseline, 3 months post-intervention , and 6 months post-intervention.
Unit of Measure: Mean score on perceived loneliness.
Time frame: At baseline, 3 months post-intervention , and 6 months post-intervention.
Unit of Measure: Time in seconds.
Time frame: At baseline, 3 months post-intervention , and 6 months post-intervention.
Unit of Measure: Mean hours per day.
Time frame: At baseline, 3 months post-intervention , and 6 months post-intervention.
Unit of Measure: Number of visits.
Time frame: At baseline.
Unit of Measure: Percentage of eligible enrollment.
Time frame: At 3 months post-intervention and 6 months post-intervention.
Unit of Measure: Mean score on satisfaction.
Time frame: At 3 months post-intervention.
Unit of Measure: Thematic analysis of interview records.
Time frame: Ongoing monitoring during intervention.
Unit of Measure: 1). Number and reasons for missed sessions; 2). Percentage of sessions meeting fidelity criteria.
Time frame: At 6 months post-intervention.
Unit of Measure: 1). Incremental cost-effectiveness ratio (ICER) per additional quality adjusted life year (QALY) gained; 2). Number and reasons of dropout.
Time frame: At 3 months post-intervention.
Unit of Measure: Thematic analysis of interview records.
Contact information is provided by the study sponsor or research team.
The Hong Kong Polytechnic University
Other
Empowering Homebound Older Adults in Self-care Using a Mobile Health-assisted, Person-centred Care Approach: A Hybrid Effectiveness-implementation Design
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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