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A Multi-Center Clinical Study of Long-Range Home Cardiac Rehabilitation

A Multi-Center Clinical Study of Long-Range Home Cardiac Rehabilitation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044063
Enrollment
Unknown
Registered
2021-03-09
Start date
2021-03-26
Completion date
Unknown
Last updated
2021-07-21

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

Conditions

Cardiovascular disease/Cardiac rehabilitation

Interventions

Study Group:CPET
Study Group:6MWT
Study Group:Physical Fitness Assessment Form
Study Group:MLWHFQ
Study Group:ADL
Study Group:PHQ-9
Study Group:GAD-7
Study Group:FTND
Study Group:ECG monitoring of dynamic ECG recorder
Control Group:CPET
Control Group:6MWT
Control Group:Physical Fitness Assessment Form
Control Group:MLWHFQ
Control Group:ADL
Control Group:PHQ-9
Control Group:GAD-7
Control Group:FTND

Sponsors

Zhejiang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Aged >= 18 years, regardless of gender; (2) Because of cardiovascular disease (such as CHD, After PCI, hypertension, PAO, cardiac arrhythmia, CHF, etc.) after hospitalization, discharged patients, and outpatients; (3) The risk level is low or medium; (4) Sign informed consent; (5) Relevant patients considered suitable for inclusion by the researchers.

Exclusion criteria

Exclusion criteria: (1) Unstable angina pectoris; (2) Patients with systolic pressure > 200mmHg or diastolic pressure > 110mmHg at rest or patients with blood pressure drop > 20mmHg and symptoms after standing up; (3) Severe aortic stenosis; (4) Acute systemic disease or fever; (5) Uncontrolled severe atrial or ventricular arrhythmia, uncontrolled significant sinus tachycardia (>120 beats/min) ; (6) Uncontrolled heart failure, third degree atrioventricular block with no pacemaker; (7) Active pericarditis or myocarditis, thrombophlebitis, recent thromboembolism, ST segment depression or elevation at rest (>2 mm); (8) Severe motor system abnormalities that can limit exercise ability and other metabolic abnormalities, such as acute thyroiditis, hypokalemia, hyperkalemia or hypovolemia; (9) Gestation period; (10) Patients with severe mental illness or dementia who cannot cooperate; (11) Patients considered unsuitable by the researchers.

Design outcomes

Primary

MeasureTime frame
VO2peak, ml/min;VO2max,ml /min/kg;AT, ml/min;METs;FVC;FEV1;FEV1/FVC;6MWTPositioning walking distance;Incidence of cardiovascular adverse events;

Secondary

MeasureTime frame
Physical Fitness Assessment Form;MLWHFQ;ADL;PHQ-9;GAD-7;FTND;

Countries

China

Contacts

Public ContactYan Jing

Zhejiang Hospital

zjicu@vip.163.com+86 13336188688

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026