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Effect evaluation of Mobile Health-based Secondary Prevention and Rehabilitation Strategies for Elderly Coronary Heart Disease Patients in Community

Research on the secondary prevention and rehabilitation management strategy of community elderly coronary heart disease based on mobile medicine and its effect evaluation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095696
Enrollment
Unknown
Registered
2025-01-10
Start date
2025-02-01
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Coronary Heart Disease

Interventions

Management group:Secondary prevention and rehabilitation management based on mobile health
Control group:Routine management

Sponsors

Fuwai Hospital, Chinese Academy of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Signed informed consent for the study; 2. Age>=65 years old and < 80 years old; 3. Diagnosed coronary heart disease for more than 1 month, including myocardial infarction and angina; Angina was only included in cases of angina undergoing percutaneous transluminal coronary angioplasty/stenting, and/or coronary artery bypass grafting; 4. It is expected that there will be no interruption in participating in the project within 1 year; 5. Clear awareness, comprehension ability, able to communicate with the researcher in writing or language, and able to cooperate with the completion of the research process; 6. Those who have not participated in drug clinical trials or other investigators during the study cycle.

Exclusion criteria

Exclusion criteria: 1. The risk stratification of exercise rehabilitation in patients with coronary heart disease is high-risk; 2. Unstable angina pectoris or myocardial infarction, worsening heart failure, acute deep vein thrombosis, pulmonary embolism, myocarditis or endocarditis within 1 month; 3. Patients with serious diseases such as hemiplegia or life expectancy of less than 1 year; 4. Those who are unable to exercise due to fractures, joint instability or other physical diseases; 5. Those who have skin diseases or injuries around the wearing part of the monitoring equipment; 6. Those who are mentally ill, epilepsy or other diseases that cause involuntary physical movement or are unable to cooperate; 7. Those with limb disability; 8. Tourette's syndrome or inability to maintain arm stability; 9. Those who are judged by the investigator not to meet the conditions for participating in the study.

Design outcomes

Primary

MeasureTime frame
Maximal oxygen consumption;Blood pressure level;

Secondary

MeasureTime frame
Quality of life;Blood glucose level;Lipid levels;Re - hospitalization;Cost-effectiveness;Adverse Events;Compliance and satisfaction of the management group ;Differences in MACE events ;

Countries

China

Contacts

Public ContactWang Zengwu

Fuwai Hospital, Chinese Academy of Medical Science

wangzengwu@foxmail.com+86 136 0136 6932

Outcome results

None listed

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