A Multi-level and Mixed-method Impact Evaluation for the Jockey Club Elders Get Active Fitness Campaign
- Conditions
- Aging Well
- Interventions
- Behavioral: Equipment boxBehavioral: Equipment box with briefingBehavioral: Exercise training with behavioral modificationBehavioral: Exercise training
- Registration Number
- NCT05908539
- Lead Sponsor
- The University of Hong Kong
- Brief Summary
The goal of this clinical trial is provide a scientific evaluation on the impact of the Jockey Club Get Fitness Campaign to improve the physical capacity and health condition of the community-dwelling older adults after the COVID-19 pandemic. Participants will take part in any of the four care models:
* a box of exercise equipment
* a box of exercise equipment with verbal briefing
* a box of exercise equipment and engage in the 8-week group-based exercise training
* receive the wonderful box of exercise equipment and engage in the 8-week group-based exercise training together with the 6-week behavioral modification
Participants with greater physical dependency, greater chronic disease burden or lower motivation for social engagement will take part in any of the three care models:
* a box of exercise equipment only
* a box of exercise equipment with verbal briefing
* a box of exercise equipment and engage in the 4-session home-based exercise training, together with the 6-week behavioral modification
- Detailed Description
This clinical trial is a mixed-method study which uses multi-level design to compare the effects of different program care models on behavioral and health-related outcomes among two different cohort of community-dwelling older adults. Exercise level and self-efficacy, physical capacity, social connectivity, geriatric symptoms, and health status are measured. A total of 1300 participants will be recruited. Outcome evaluation 8 weeks after intervention and 3 months after intervention will be included to allow the detection of immediate and long-term program benefits. In-depth individual and focus-group interviews will be conducted to solicit the participants' experience and perceived benefits of the program.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 1057
- Age above 60 years
- Resident of public rental house
- Any contraindication to exercise training
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Equipment box (general) Equipment box A box of exercise equipment is distributed to community dwelling older adults. Equipment box (home-bound) Equipment box A box of exercise equipment is distributed to home-bound community dwelling older adults. Equipment box with briefing (home-bound) Equipment box with briefing A box of exercise equipment is distributed. Verbal briefing of exercise equipment is provided to home-bound community dwelling older adults. Home-based exercise with behavioral modification (home-bound) Exercise training with behavioral modification A box of exercise equipment is distributed. Verbal briefing of exercise equipment and an 8-week group exercise training program is provided to home-bound community dwelling older adults, following by a 6-week behavioral modification. Equipment box with briefing (general) Equipment box with briefing A box of exercise equipment is distributed. Verbal briefing of exercise equipment is provided to community dwelling older adults. Group-based exercise (general) Exercise training A box of exercise equipment is distributed. Verbal briefing of exercise equipment and an 8-week group exercise training program is provided to community dwelling older adults. Group-based exercise with behavioral modification (general) Exercise training with behavioral modification A box of exercise equipment is distributed. Verbal briefing of exercise equipment and an 8-week group exercise training program is provided to community dwelling older adults, following by a 6-week behavioral modification.
- Primary Outcome Measures
Name Time Method Step count Changes from baseline to 8 weeks after start intervention Step count per day measured by a pedometer
Insomnia risk score Changes from baseline to 8 weeks after start intervention Measured by Insomnia Severity Index questionnaire (range0-28), higher score greater severity of insomnia
Loneliness score Changes from baseline to 8 weeks after start intervention Measured by UCLA Loneliness Scale questionnaire (range20-80), higher score greater loneliness
Mobility limitation score Changes from baseline to 8 weeks after start intervention Measured by Short Physical Performance Battery (range 0-12), higher score better physical performance
Mental health score Changes from baseline to 8 weeks after start intervention Measured by Mental Health Inventory questionnaire (range 0-100), higher score better mental health
Sarcopenia risk score Changes from baseline to 8 weeks after start intervention Measured by Sarcopenia(SARC) questionnaire and calf circumference in unit of cm (range0-20), higher score higher risk of sarcopenia
Frailty risk score Changes from baseline to 8 weeks after start intervention Measured by Edmonton Frail Scale questionnaire (range0-17), higher score more severer frailty
Exercise self-efficacy score Changes from baseline to 8 weeks after start intervention Score measured by Self-Efficacy for Exercise Scale questionnaire (range 0-90), higher score higher self-efficacy for exercise
Performance of timed up-and-go test Changes from baseline to 8 weeks after start intervention Measured by timed up-and-go test in unit of second
Fatigue score Changes from baseline to 8 weeks after start intervention Measured by Brief Fatigue Inventory questionnaire (range0-10), higher score greater fatigue
Functional mobility score Changes from baseline to 8 weeks after start intervention Score measured by Life Space Assessment questionnaire (range: 0-120), higher score better performance
Hand grip strength Changes from baseline to 8 weeks after start intervention Hand grip strength measured by hand-held dynamometer in unit of KG
Social connectedness score Changes from baseline to 8 weeks after start intervention Measured by Social Connectedness Scale questionnaire (20-100), higher score stronger social connectedness
Health status self-rated score Changes from baseline to 8 weeks after start intervention Measured by EQ05D-5L questionnaire (range -0.59-1.0), higher score better quality of life
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
Trial Locations
- Locations (1)
The University of Hong Kong
🇭🇰Hong Kong, Hong Kong