Skip to content

Effect of Resistance Training in Adults With Complex Congenital Heart Disease

Effect of Resistance Training in Adults With Complex Congenital Heart Disease

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02658266
Enrollment
40
Registered
2016-01-18
Start date
2016-02-29
Completion date
2019-02-28
Last updated
2017-09-14

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

Conditions

Congenital Heart Defect

Keywords

resistance training, adult, muscle strength, muscle endurance, muscle metabolism

Brief summary

Adults with complex congenital heart disease have impaired muscle function compared both to health controls and patients with lesions classified as simple. There is only one study assessing the effects of resistance training in patients palliated with Fontan procedure. The hypotheses of the present study is that home based resistance training will improve muscle function in adults with different complex congenital hear diseases.

Detailed description

The number of adults with complex congenital heart disease is increasing and today they outnumber the children with corresponding lesions. However, the longterm prognosis is still unknown and continuously changing as new therapeutic options are introduced. Patients with complex congenital heart disease have reduced muscle function compared to healthy controls as well as patients with lesions classified as simple. Furthermore, men with congenital heart disease are more commonly underweight and less commonly overweight obese compared to the general population. In addition, men with complex lesions are shorter in comparison to controls. This indicates an altered body composition i.e. muscle mass, fat mass and bone density in this population. Moreover, impaired muscle metabolism has been reported in patients palliated with Fontan procedure. Adult patients with complex congenital heart disease will be recruited based on defined inclusion and exclusion criteria. Muscle function, muscle strength, muscle metabolism and body composition will be evaluated before randomisation and at follow-up after twelve weeks. The patients will be randomised to twelve weeks of home based resistance training or to a control group. The randomisation ratio will be 1:1 ( intervention:control). The control group will be instructed to continue with their habitual physical activities. The resistance training protocol will be individualised based on the results of the muscle function and muscle strength tests. The aim of this study is to investigate the effects of resistance training on muscle function, muscle strength, body composition and muscle metabolism in adults with complex congenital heart disease.

Interventions

BEHAVIORALHome based resistance training

The participants in the intervention group will receive an individualized resistance training program. The individual adjustments in load will will be made from the results of the muscle function and muscle strength tests. The resistance training will be home based and performed 3 times per week 10-12 reps 2 sets 12 weeks. Increment of load will be performed continuously according to rating of perceived exertion.

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Complex congenital heart disease ( e.g. tetralogy of Fallot, transposition of the great arteries, pulmonary atresia, patients palliated with Fontan procedure or total cavo-pulmonary connection). * Clinically stable without significant change the last 3 months. * Adult (\> 18 years of age). * Informed consent.

Exclusion criteria

* Cognitive impairment affecting the ability of independent decision making. * Present strategy of regularly executing resistance training \> 2times per week in purpose to increase muscle strength. * Other comorbidity affecting physical activity. * Other circumstance making participation unsuitable.

Design outcomes

Primary

MeasureTime frame
Change in muscle strength (Newton, N)Change from baseline muscle strength at 12 weeks follow-up

Secondary

MeasureTime frameDescription
Change in muscle endurance (number of repetitions)Change from baseline muscle endurance at 12 weeks follow-up
Change in total body skeletal muscle mass (kg)Change from baseline total body skeletal muscle mass at 12 weeks follow-upUsing dual-energy x-ray absorptiometry (DEXA)
Change in appendicular skeletal muscle mass (kg)Change from baseline appendicular skeletal muscle mass at 12 weeks follow-upUsing dual-energy x-ray absorptiometry (DEXA)
Change in bone mineral density (g/cm2)Change from baseline bone mineral density at 12 weeks follow-upUsing dual-energy x-ray absorptiometry (DEXA)
Muscle metabolismChange from baseline muscle metabolism at 12 weeks follow-upnear infrared spectroscopy (NIRS)
Change in body fat percentageChange from baseline body fat percentage at 12 weeks follow-upUsing dual-energy x-ray absorptiometry (DEXA)

Other

MeasureTime frameDescription
Compliance to study protocolAt completion of study protocol 12 weeksnumber of training sessions
Adverse eventsOnce a week from the date of onset of the home based exercise regimen until the followup at 12 weeksComplications to resistance training

Countries

Sweden

Contacts

Primary ContactBengt Johansson, MD, PhD
bengt.johansson@medicin.umu.se+46907852782
Backup ContactCamilla Sandberg, PhD stud
camilla.sandberg@medicin.umu.se+46907858441

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026