Skip to content

Cardiac rehabilitation/fitness (CardiFIT) for children with congenital heart disease

The Effectiveness of Cardiac rehabilitation/fitness (CardiFIT) for children with congenital heart disease: A prospective, randomized, open-label, parallel-controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040354
Enrollment
Unknown
Registered
2020-11-28
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-02-16

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

Conditions

Congenital Heart Disease

Interventions

Experimental group:Remote cardiac rehabilitation/fitness (CardiFIT)

Sponsors

West China Second University Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 18 Years

Inclusion criteria

Inclusion criteria: (1) Male or female aged 5 to 18 years old; (2) Patients with a CHD, as defined by the international ACC-CHD classification; (3) CPET performed within the last 3 months with VO2max < 80% of predicted VO2max or VAT < 50% of predicted VO2max; (4) Patients/their guardians have basic information literacy, own smart mobile terminals (such as cells, tablets, etc.), and can skillfully operate mobile applications; (5) Written informed consent.

Exclusion criteria

Exclusion criteria: (1) Absolute contraindications for CPET: fever, uncontrolled asthma, respiratory failure, acute myocarditis or pericarditis, severe hypertrophic obstructive cardiomyopathy, uncontrolled arrhythmias causing symptoms or haemodynamic compromise, uncontrolled heart failure, uncontrolled hypertension, acute pulmonary embolus or pulmonary infarction, symptomatic aortic stenosis, and children with mental impairment leading to inability to cooperate; (2) Recent (<3 months) intracardiac thrombus, embolism, or thrombophlebitis; (3) Cardiac surgery planned during the study; (4) Patient who have undertaken cardiac rehabilitation within the last 24 months; (5) Acute systemic illness or severe musculoskeletal abnormalities; (6) Patients with a severe intellectual disability that does not allow the completion of the quality of life questionnaire; (7) Patients participating in concurrent interventional research which may overburden the patient or confound data collection; (8) Patients considered being unable to participate in the study for any other reason (for example, psychiatric disorder, dementia, life-threatening comorbidity, etc.).

Design outcomes

Primary

MeasureTime frame
Peak Oxygen Uptake;

Secondary

MeasureTime frame
Physical Activity Level;Health-Related Quality of Life;Cardiac Function and Structure;Body Component;Self-Perceptions of Adequacy in and Predilection for Physical Activity;Anxiety and Depression;The Activity Support Parenting;Perceiced Caregiver Burden;Care-related Quality of Life;Quality of Life;

Countries

China

Contacts

Public ContactLuo Biru

West China Second University Hospital of Sichuan University

luomr@scu.edu.cn+86 18180609180

Outcome results

None listed

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