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

Not Applicable
Active, not recruiting
Conditions
Aging Well
Interventions
Behavioral: Equipment box
Behavioral: Equipment box with briefing
Behavioral: Exercise training with behavioral modification
Behavioral: 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
Inclusion Criteria
  • Age above 60 years
  • Resident of public rental house
Exclusion Criteria
  • Any contraindication to exercise training

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Equipment box (general)Equipment boxA box of exercise equipment is distributed to community dwelling older adults.
Equipment box (home-bound)Equipment boxA box of exercise equipment is distributed to home-bound community dwelling older adults.
Equipment box with briefing (home-bound)Equipment box with briefingA 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 modificationA 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 briefingA box of exercise equipment is distributed. Verbal briefing of exercise equipment is provided to community dwelling older adults.
Group-based exercise (general)Exercise trainingA 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 modificationA 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
NameTimeMethod
Step countChanges from baseline to 8 weeks after start intervention

Step count per day measured by a pedometer

Insomnia risk scoreChanges from baseline to 8 weeks after start intervention

Measured by Insomnia Severity Index questionnaire (range0-28), higher score greater severity of insomnia

Loneliness scoreChanges from baseline to 8 weeks after start intervention

Measured by UCLA Loneliness Scale questionnaire (range20-80), higher score greater loneliness

Mobility limitation scoreChanges from baseline to 8 weeks after start intervention

Measured by Short Physical Performance Battery (range 0-12), higher score better physical performance

Mental health scoreChanges from baseline to 8 weeks after start intervention

Measured by Mental Health Inventory questionnaire (range 0-100), higher score better mental health

Sarcopenia risk scoreChanges 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 scoreChanges from baseline to 8 weeks after start intervention

Measured by Edmonton Frail Scale questionnaire (range0-17), higher score more severer frailty

Exercise self-efficacy scoreChanges 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 testChanges from baseline to 8 weeks after start intervention

Measured by timed up-and-go test in unit of second

Fatigue scoreChanges from baseline to 8 weeks after start intervention

Measured by Brief Fatigue Inventory questionnaire (range0-10), higher score greater fatigue

Functional mobility scoreChanges from baseline to 8 weeks after start intervention

Score measured by Life Space Assessment questionnaire (range: 0-120), higher score better performance

Hand grip strengthChanges from baseline to 8 weeks after start intervention

Hand grip strength measured by hand-held dynamometer in unit of KG

Social connectedness scoreChanges 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 scoreChanges 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
NameTimeMethod

Trial Locations

Locations (1)

The University of Hong Kong

🇭🇰

Hong Kong, Hong Kong

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