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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04851262
Other study ID # UW20-868
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date April 28, 2021
Est. completion date December 31, 2024

Study information

Verified date December 2023
Source The University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall aim of the proposed project is to improve muscle strength in older adults with possible sarcopenia by promoting home-based progressive resistance exercise. The target population for health talks is community-dwelling older adults. A Three monthly home-visits and weekly phone calls will be made. A waitlist randomised controlled trial will be conducted to evaluate effectiveness, and qualitative feedback will be collected from participants. A pilot study will be conducted first.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 42
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years to 89 Years
Eligibility The inclusion criteria are: - Aged 65-89; - Possible sarcopenia (defined by AWGS 2019); - No cognitive impairment (Abbreviated Mental Test score =8); and - No communication problems. The exclusion criteria are: - having engaged in a structured exercise programme in the past 6 months or planning to do so within the intervention period; - mobility-limiting injury of the hands or lower limbs, surgery or hospitalisation within the intervention period; - contraindications such as musculoskeletal/cardiorespiratory disorders, or any advanced diseases that inhibit them from exercising.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Exercise
The intervention is to be taught by fitness trainer at the participants' home at the start of each phase. The exercise progression model for older adults recommended by the American College of Sports Medicine, which emphasise gradual increments in training load and systematically alter one or more programme components, will be adopted.

Locations

Country Name City State
Hong Kong Community Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
The University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Other Change in handgrip strength at 12 weeks from baseline Measured by a spring-type dynamometer, higher value indicates better performance 12 weeks after baseline
Other Change in handgrip strength at 24 weeks from baseline Measured by a spring-type dynamometer, higher value indicates better performance 24 weeks after baseline
Other Status of possible sarcopenia at 12 weeks from baseline Indicated by 5-time chair stand test =12 second, or men and women with <28 kg and <18 kg strength 12 weeks after baseline
Other Status of possible sarcopenia at 24 weeks from baseline Indicated by 5-time chair stand test =12 second, or men and women with <28 kg and <18 kg strength 24 weeks after baseline
Other Sarcopenia risk score at 12 weeks from baseline Measured by SARC-CalF, which is a combination of SARC-F questionnaire and calf circumference, a cut of of >=11 indicates high risk 12 weeks after baseline
Other Sarcopenia risk score at 24weeks from baseline Measured by SARC-CalF, which is a combination of SARC-F questionnaire and calf circumference, a cut of of >=11 indicates high risk 24 weeks after baseline
Primary Change in lower-limb muscle strength at 12 weeks from baseline Measured by Short Physical Performance Battery (SPPB), higher score indicates better performance 12 weeks after baseline
Secondary Change in lower-limb muscle strength at 24 weeks from baseline Measured by Short Physical Performance Battery (SPPB), higher score indicates better performance 24 weeks after baseline
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