Skip to content

The Effects of Exercise Intervention on Skeletal Muscle and Other Organs in Aged Population and the Discovery of Associated Circulating Biomarkers

The Effects of Exercise Intervention on Skeletal Muscle and Other Organs in Aged Population and the Discovery of Associated Circulating Biomarkers

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06660706
Enrollment
100
Registered
2024-10-28
Start date
2024-04-01
Completion date
2026-12-31
Last updated
2024-10-28

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

Conditions

Age-related Functional Decline

Keywords

aging, muscle health, body composition

Brief summary

This project aims to investigate the intricate interplay between skeletal muscle and adipose tissue during the aging process by integrating human studies. Utilizing interventional research and randomized trials combined with examining blood samples from elderly individuals engaged in exercise, we aim to investigate the effects of exercise on muscle health and explore the underlying mechanisms of muscle aging and related biomarkers. Interdisciplinary research allowed us to investigate the systemic impact of exercise on muscles. This approach allowed us to gain a better understanding of the interconnectedness of skeletal muscle and adipose tissue in the aging process and devise efficient strategies to reverse age-related changes. These findings hold promise for promoting a future society where long and healthy life is achievable for all.

Detailed description

This study is a randomized controlled trial of 6-month multidomain intervention program among community-living older adults with early physical impairments. Inclusion criteria are: (1) community-dwelling adults aged ≥ 65 years, (2) slow gait speed (\<1 m/s in 6-meter walk test) or weakness (dominant handgrip strength \<28 kg in men, \<18 kg in women); subjects with the following conditions will be excluded: (1) established diagnosis of dementia, Parkinsonism or other neurodegenerative disease (2) disable status: mobilitylimiting conditions, (3) active, acute diseases receiving treatment, such as cancer, heart failure, COPD and so on, (4) estimated life expectancy \<12 months, (5) current nursing home residents.

Interventions

Each session comprises of 45 minutes physical fitness activities targeting on muscle strength, balance, and flexibility; 1-hour cognitive training primarily on reasoning and memory exercises; and 15-minute for nutritional advices based on national diet guidelines for older adults

Sponsors

National Health Research Institutes, Taiwan
CollaboratorOTHER
National Yang Ming Chiao Tung University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* aged ≥ 65 years * slow gait speed (\<1 m/s in 6-meter walk test) or weakness (dominant handgrip strength \<28 kg in men, \<18 kg in women)

Exclusion criteria

* established diagnosis of dementia, Parkinsonism or other mobility-limiting, disable conditions * active, acute diseases receiving treatment, such as cancer, heart failure, COPD and so on * estimated life expectancy \<12 months * current nursing home residents

Design outcomes

Primary

MeasureTime frameDescription
Change in Physical performancebaseline, 6 monthChange in hand-grip strength (kg), or six-meter walking speed (m/s), or 5 times sit to stand test from baseline to 6 months in all participants

Secondary

MeasureTime frameDescription
Change in IGF-1baseline, 6 monthChange in IGF-1 concentration from baseline to 6 months in all participants
Change in hs-CRPbaseline, 6 monthChange in hs-CRP concentration from baseline to 6 months in all participants
Change in Myostatinbaseline, 6 monthChange in Myostatin concentration from baseline to 6 months in all participants
Change in Activing Abaseline, 6 monthChange in Activing A concentration from baseline to 6 months in all participants
Change in DHEA-Sbaseline, 6 monthChange in DHEA-S concentration from baseline to 6 months in all participants
Change in Relative appendicular skeletal muscle index (RASM)baseline, 6 monthChange in RASM from baseline to 6 months in all participants
Change in body fat %baseline, 6 monthChange in body fat % from baseline to 6 months in all participants
Change in Cognitive performancebaseline, 6 monthChange in Montreal Cognitive Assessment (MoCA), or Mini-mental state examination (MMSE) from baseline to 6months in all participants
Change from lipoprofliebaseline, 6 monthChange in Total Cholesterol, Triglyceride, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol from baseline to 6months in all participants
Change in Follistatinbaseline, 6 monthChange in Follistatin concentration from baseline to 6 months in all participants

Countries

Taiwan

Contacts

Primary ContactLi-Ning Peng, M.D., PhD
lining.peng@gmail.com+886-28239014

Outcome results

None listed

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