Skip to content

Home-based Progressive Resistance Exercise to Enhance Physical Performance of Older Adults With Possible Sarcopenia

Home-based Progressive Resistance Exercise to Enhance Physical Performance of Older Adults With Possible Sarcopenia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04851262
Enrollment
42
Registered
2021-04-20
Start date
2021-01-01
Completion date
2024-11-07
Last updated
2025-03-28

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

Conditions

Sarcopenia

Brief 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.

Interventions

BEHAVIORALExercise

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.

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
65 Years to 89 Years
Healthy volunteers
Yes

Inclusion criteria

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in lower-limb muscle strength at 12 weeks from baseline12 weeks after baselineMeasured by Short Physical Performance Battery (SPPB), higher score indicates better performance

Secondary

MeasureTime frameDescription
Change in lower-limb muscle strength at 24 weeks from baseline24 weeks after baselineMeasured by Short Physical Performance Battery (SPPB), higher score indicates better performance

Other

MeasureTime frameDescription
Status of possible sarcopenia at 24 weeks from baseline24 weeks after baselineIndicated by 5-time chair stand test ≥12 second, or men and women with \<28 kg and \<18 kg strength
Change in handgrip strength at 12 weeks from baseline12 weeks after baselineMeasured by a spring-type dynamometer, higher value indicates better performance
Change in handgrip strength at 24 weeks from baseline24 weeks after baselineMeasured by a spring-type dynamometer, higher value indicates better performance
Sarcopenia risk score at 24weeks from baseline24 weeks after baselineMeasured by SARC-CalF, which is a combination of SARC-F questionnaire and calf circumference, a cut of of \>=11 indicates high risk
Sarcopenia risk score at 12 weeks from baseline12 weeks after baselineMeasured by SARC-CalF, which is a combination of SARC-F questionnaire and calf circumference, a cut of of \>=11 indicates high risk
Status of possible sarcopenia at 12 weeks from baseline12 weeks after baselineIndicated by 5-time chair stand test ≥12 second, or men and women with \<28 kg and \<18 kg strength

Countries

Hong Kong

Outcome results

None listed

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