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Impact of Cardiac Rehabilitation-Guided Health Maintenance Programs in the Elderly

Impact of Cardiac Rehabilitation-Guided Health Maintenance Programs on Negative Events in the Elderly: An Observational Prospective Study Protocol

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000032404
Enrollment
Unknown
Registered
2020-04-27
Start date
2021-02-20
Completion date
Unknown
Last updated
2020-04-27

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

Conditions

Negative Events in the Elderly

Interventions

A:comprehensive health maintenance plan
B:basic health maintenance plan

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged over 65 years; 2. To be able to complete the 400-m walk test within 15 min without sitting, the help with another person or the use of a walker; 3. Willingness to accept the 12-month follow-up and conduct study-related exercise plan.

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. 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
negative event;

Secondary

MeasureTime frame
cardiac pulmonary capacity;Cardiac ultrasound parameters;Activities of daily living;quality of life;Laboratory examination;

Countries

China

Contacts

Public ContactQiaowei Li

Fujian Provincial Hospital

docjovylee@hotmail.com+86 15980232545

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026