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Research and Empirical Study on the Development of a Personalized Exercise Rehabilitation System for Elderly Patients with Cardiovascular Disease and Frailty Suffering from Kinesiophobia

Research and Empirical Study on the Development of a Personalized Exercise Rehabilitation System for Elderly Patients with Cardiovascular Disease and Frailty Suffering from Kinesiophobia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114785
Enrollment
Unknown
Registered
2025-12-17
Start date
2025-12-17
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Patients with cardiovascular diseases in the elderly who are also suffering from frailty

Interventions

Personalized Sports Rehabilitation Group:Personalized Sports Rehabilitation Recommendation System
Control group:conventional cardiovascular disease exercise rehabilitation guidance

Sponsors

Xiamen Cardiovascular Hospital Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Age >= 60 years; 2.Clearly diagnosed with cardiovascular diseases (including coronary heart disease, hypertension, chronic heart failure, etc.); 3.Evaluated as being in a state of frailty by the frailty assessment tool set; 4.Without significant cognitive impairment, able to understand and follow exercise instructions.

Exclusion criteria

Exclusion criteria: 1.Have a history of severe cardiovascular events, such as acute myocardial infarction, unstable angina pectoris, etc., and the condition is not well controlled; 2.have severe complications in the respiratory system, nervous system, musculoskeletal system, etc., which affect the exercise ability; 3.have aphasia, confusion of consciousness, inability to cooperate with assessment, and inability to communicate; 4.cannot tolerate exercise or have exercise contraindications; 5.patients who have participated in intervention clinical trials that may affect the research results within 3 months before the assessment.

Design outcomes

Primary

MeasureTime frame
kinesiophobia;Frailty;

Secondary

MeasureTime frame
Exercise Social Support;Readmission rate;Quality of life;Adverse event;Exercise Self-Efficacy;Physical activity level;Somatic symptoms;System availability;mortality rate;

Countries

China

Contacts

Public ContactChen Yuan

Xiamen Cardiovascular Hospital Xiamen University

28837445@qq.com+86 592 299 3237

Outcome results

None listed

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