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A real-world study of exercise improving aging and frailty

A real-world study of exercise improving aging and frailty

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081824
Enrollment
Unknown
Registered
2024-03-13
Start date
2021-04-01
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

Aging and frailty

Interventions

Exercise:Exercise training
Control:healthy lifestyle

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 90 Years

Inclusion criteria

Inclusion criteria: non-disabled old adults aged 65 to 85 years old, who can walk 400 meters in 15 minutes without the help of another person or the assistance of a walker, and voluntarily to accept at least 1-year follow-up and a study-related exercise program.

Exclusion criteria

Exclusion criteria: 1. 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, 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 low room air desaturation at rest (=85%); 7. Other severe uncontrolled diseases (hypertension, diabetes, thyrotoxicosis, severe renal insufficiency, infection); 8. Moderate to severe cognitive dysfunction (MMSE=20), mental impairment leading to inability to cooperate; 9. Circumstances such as atrial fibrillation, frequent premature contractions, or the presence of metal implants in the chest and abdominal cavity where cardiac magnetic resonance imaging cannot be performed; 10. Difficulty communicating with the study personnel due to speech, language, hearing or visual problems; 11. Inability or unwillingness to provide informed consent or accept follow-up.

Design outcomes

Primary

MeasureTime frame
change of peak Oxygen uptake/kg;

Secondary

MeasureTime frame
changes of maximal work rate, peak oxygen uptake, anaerobic threshold, work efficiency, static ventilation function and ventilatory efficiency during exercise;changes of static cardiac structure and function;changes of geriatric assessments of function, body composition and agerelated biomarkers;

Countries

China

Contacts

Public ContactPengli Zhu

Fujian Provincial Hospital

zpl7755@hotmail.com+86 137 9995 7755

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 17, 2026