Exercise Training in Children With Congenital Heart Defect
The purpose of this study was to investigate the effects of exercise training on exercise capacity, physical activity (PA), health-related quality of life (HRQoL), and the psychosocial factors affecting PA in sedentary congenital heart defect (CHD) children and healthy sedentary children. The degree of improvement after exercise training were compared between CHD children and healthy sedentary...
Brief Summary
Official Title: “The Effect of Exercise Training on Exercise Capacity, Physical Activity, and Health-related Quality of Life in Children After Repair of Congenital Heart Defect”
The purpose of this study was to investigate the effects of exercise training on exercise capacity, physical activity (PA), health-related quality of life (HRQoL), and the psychosocial factors affecting PA in sedentary congenital heart defect (CHD) children and healthy sedentary children. The degree of improvement after exercise training were compared between CHD children and healthy sedentary children.
- Study Type: Interventional
- Study Design: Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
- Study Primary Completion Date: June 2008
Detailed Clinical Trial Description
Exercise groups took 12-week exercise training, twice in hospital and once at home, using a video game so-called Dance Dance Revolution (DDR), while the control group kept their daily routines.
Intervention(s) in this Clinical Trial
- Other: Exercise
- Using a video game so-called Dance Dance Revolution (DDR)
Arms, Groups and Cohorts in this Clinical Trial
- Other: Exercise
- Dance Dance Revolution (DDR)
Outcome Measures for this Clinical Trial
Primary Measures
- maximal treadmill exercise test
- Time Frame: 12 wks
Safety Issue?: No
- Time Frame: 12 wks
Criteria for Participation in this Clinical Trial
Inclusion Criteria:
- Children with congenital heart defect s/p repair > 6 months
- Sedentary lifestyle
Exclusion Criteria:
- Unstable hemodynamics
- Impaired mental and cognition
- Systemic disease
Gender Eligibility for this Clinical Trial: Both
Minimum Age for this Clinical Trial: 7 Years
Maximum Age for this Clinical Trial: 16 Years
Are Healthy Volunteers Accepted for this Clinical Trial?: Accepts Healthy Volunteers
Clinical Trial Investigator Information
Lead Investigator: National Taiwan University Hospital Other
Additional Information
Information obtained from ClinicalTrials.gov on February 12, 2012
Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00930800
Study ID Number: 200712010R
ClinicalTrials.gov Identifier: NCT00930800
Health Authority: Taiwan: Department of Health
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The URL of this page is:
http://clinicaltrialsfeeds.org/clinical-trials/show/NCT00930800
