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A Multi-level and Mixed-method Impact Evaluation for the Jockey Club Elders Get Active Fitness Campaign

A Multi-level and Mixed-method Impact Evaluation for the Jockey Club Elders Get Active Fitness Campaign

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05908539
Enrollment
1057
Registered
2023-06-18
Start date
2023-01-02
Completion date
2025-08-31
Last updated
2025-12-17

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

Conditions

Aging Well

Keywords

Aging, Community-dwelling, Exercise, Care model

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.

Interventions

BEHAVIORALEquipment box

Participants receive a box of exercise equipment containing dumbbell, elastic band, hand cycle machine, and booklet of exercise instruction only.

BEHAVIORALEquipment box with briefing

Participants receive a box of exercise equipment containing dumbbell, elastic band, hand cycle machine, and booklet of exercise instruction, and they are given verbal briefing on how to use the equipment.

BEHAVIORALExercise training

Participants receive al box of exercise equipment. They attend an 8-week group exercise training program for 1 hour /session and 1 session/ week, and are supervised by a physical fitness training. The exercise program includes a combination of aerobic, resistance, balance and flexibility exercises.

BEHAVIORALExercise training with behavioral modification

Participants receive al box of exercise equipment. They attend an 8-week group exercise training program for 1 hour /session and 1 session/ week, and are supervised by a physical fitness training. The exercise program includes a combination of aerobic, resistance, balance and flexibility exercises. After finishing the exercise training program, a 6-week behavioral modification is provided. Two home visits and four telephone visits are conducted to empower the participants for exercise at home.

Sponsors

The Hong Kong Jockey Club Charities Trust
CollaboratorOTHER
The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age above 60 years * Resident of public rental house

Exclusion criteria

* Any contraindication to exercise training

Design outcomes

Primary

MeasureTime frameDescription
Step countChanges from baseline to 8 weeks after start interventionStep count per day measured by a pedometer
Functional mobility scoreChanges from baseline to 8 weeks after start interventionScore measured by Life Space Assessment questionnaire (range: 0-120), higher score better performance
Exercise self-efficacy scoreChanges from baseline to 8 weeks after start interventionScore measured by Self-Efficacy for Exercise Scale questionnaire (range 0-90), higher score higher self-efficacy for exercise
Hand grip strengthChanges from baseline to 8 weeks after start interventionHand grip strength measured by hand-held dynamometer in unit of KG
Performance of timed up-and-go testChanges from baseline to 8 weeks after start interventionMeasured by timed up-and-go test in unit of second
Mobility limitation scoreChanges from baseline to 8 weeks after start interventionMeasured by Short Physical Performance Battery (range 0-12), higher score better physical performance
Sarcopenia risk scoreChanges from baseline to 8 weeks after start interventionMeasured by Sarcopenia(SARC) questionnaire and calf circumference in unit of cm (range0-20), higher score higher risk of sarcopenia
Frailty risk scoreChanges from baseline to 8 weeks after start interventionMeasured by Edmonton Frail Scale questionnaire (range0-17), higher score more severer frailty
Social connectedness scoreChanges from baseline to 8 weeks after start interventionMeasured by Social Connectedness Scale questionnaire (20-100), higher score stronger social connectedness
Insomnia risk scoreChanges from baseline to 8 weeks after start interventionMeasured by Insomnia Severity Index questionnaire (range0-28), higher score greater severity of insomnia
Mental health scoreChanges from baseline to 8 weeks after start interventionMeasured by Mental Health Inventory questionnaire (range 0-100), higher score better mental health
Fatigue scoreChanges from baseline to 8 weeks after start interventionMeasured by Brief Fatigue Inventory questionnaire (range0-10), higher score greater fatigue
Loneliness scoreChanges from baseline to 8 weeks after start interventionMeasured by UCLA Loneliness Scale questionnaire (range20-80), higher score greater loneliness
Health status self-rated scoreChanges from baseline to 8 weeks after start interventionMeasured by EQ05D-5L questionnaire (range -0.59-1.0), higher score better quality of life

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026