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Effect of formatted resistance training on muscle mass and function in the elderly

Effect of formatted resistance training on muscle mass and function in the elderly: a random control trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062007
Enrollment
Unknown
Registered
2022-07-19
Start date
2022-07-20
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

sarcopenia

Interventions

control:resistance training less than once per week
low frequency:resistance training twice to three times per week
high frequency:resistance training three to five times per week

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged and over 65; 2. Ability to complete the 400-m walk test within 15 min without sitting, the help of another person or the use of a walker; 3. Willingness to follow the study protocol and conduct study-related exercise programs.

Exclusion criteria

Exclusion criteria: 1. Acute acute myocardial infarction (3-5 days), unstable angina pectoris, resting electrocardiogram suggesting an acute cardiac event; 2. Active endocarditis, myocarditis, or pericarditis; 3. Uncontrolled arrhythmias causing symptoms or hemodynamic compromise, the high-degree atrioventricular block without pacemaker; 4. Acute congestive heart failure or heart function Grade III-IV (New York Classification); 5. Aortic dissection, aortic aneurysm, or severe valvular disease; 6. Uncontrolled asthma, pulmonary edema, significant pulmonary hypertension, or room air desaturation at rest (85%); 7. Severe uncontrolled other diseases (hypertension, diabetes, thyrotoxicosis, severe renal insufficiency, infection); 8. Moderate to severe cognitive dysfunction (MMSE=20 or CDR=2), mental impairment leading to inability to cooperate; 9. Difficulty communicating with the study personnel due to speech, language, hearing, or visual problems; 10. Inability or unwillingness to provide informed consent or accept follow-up.

Design outcomes

Primary

MeasureTime frame
grip;

Countries

China

Contacts

Public ContactQiaowei Li

Fujian Provincial Hospital

357029756@qq.com+86 15980232545

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026