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Home-based Psychoeducation for Older Adults With Frailty: A Feasibility Trial

Effects of A Home-based Psychoeducation Programme on Subjective Well-being for Older Adults With Frailty in the Community: A Feasibility Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06415617
Enrollment
24
Registered
2024-05-16
Start date
2023-11-24
Completion date
2024-04-09
Last updated
2024-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frailty, Well-Being, Psychological

Keywords

Subjective well-being, frailty, psychoeducation

Brief summary

This study aims to test the feasibility and acceptability of home-based psychoeducation in older adults with frailty in the community. The main questions it aims to answer are 1. Are the proposed eligibility criteria for participants and the study process in recruiting and retaining the participants appropriate? 2. Is home-based psychoeducation feasible and acceptable for older adults with frailty in the community? Participants will receive 12 weekly online group-based sessions at their homes. The content for the experimental group and control group is different: * Intervention group: psychoeducation * Control group: physical health education Participants will receive two home visits for data collection. An individual interview will be conducted with participants in the experimental group to explore their experiences.

Interventions

OTHERPsychoeducation

The content of psychoeducation is based on Five Ways of Well-being which covers Be active, Connect, Take Notice, Keep learning and Giving . The participants will be engaged in psychoeducation through group discussion, individualised goal setting and reflective exercises.

OTHERAttention control

The content of the sessions mainly focuses on physical health information, such as healthy eating, physical exercise, prevention of falls, and pain management.

Sponsors

TAO An
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

(1) aged 65 years or over; (2) meeting frailty criteria by FRAIL scale (score 3 or above) ; (3) mentally competent screened by The Abbreviated Mental Test (AMT≥6) ; (4) able to speak and understand Cantonese; (5) living at home; (6) having experience using a smartphone (e.g.: sending messages, watching videos)

Exclusion criteria

(1) have a visual or hearing problem or a language barrier that may affect their communication or understanding; (2) being unfit for home-based exercise, as defined by having one point or above at either the 25-item Home Falls and Accidents self-reported screening tool (HOME-FAST), which is a comprehensive tool for identify home hazards for fall (3) are currently practising exercise for at least 150 minutes per week in previous four weeks; (4) are receiving active psychiatric or antidepressant treatment or joining other physical exercises or rehabilitation programmes

Design outcomes

Primary

MeasureTime frameDescription
Participation rate, self-reported intervention adherence, and attrition rate.12 weeks post-allocationThe feasibility of the study will be measured in terms of participation rate, self-reported intervention adherence, and attrition rate.
Acceptability12 weeks post-allocationA 5-item satisfaction survey will be conducted by the end of the intervention for participants to rate the intervention in terms of appropriates of the session content, length of each session, overall intervention duration and delivery mode, from 1 (very dissatisfied) to 5 (very satisfied).

Secondary

MeasureTime frameDescription
Activities of daily living12 weeks post-allocationKatz Index of Independence in Activities of Daily Living
Instrumental activities of daily living12 weeks post-allocationLawton Instrumental Activities of Daily Living Scale
Subjective well-being12 weeks post-allocationThe Chinese 5-item World Health Organization Well-Being Index
Frailty level12 weeks post-allocationFRAIL scale
Social support12 weeks post-allocation10-item Duke Social Support Index
Quality of life12 weeks post-allocationEuroQol 5-Dimension 5-Level
Depressive symptoms12 weeks post-allocation4-item Geriatric Depression scale
Physical functioning12 weeks post-allocationThe Senior Fitness Test: It covers four dimensions, including muscle endurance, balance, flexibility, and tolerance measured by 30-sec arm-curl test, 30-sec chair-stand test, back-scratch test, chair sit-and-reach test, 8-foot up-and-go test, two-min step test.

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 1, 2026