Effect of Muscle Strengthening Training in Adults With Fontan Circulation

Congenital Heart Disease Clinical Trial

Official title:

Effect of Muscle Strengthening Training in Adults With Fontan Circulation Compared to Healthy Controls

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05454254
• Other study ID #: Muscle training Fontan
• Status: Recruiting
• Phase: N/A
• Start date: August 15, 2022
• Est. completion date: November 30, 2023

Study information

• Verified date: May 2023
• Source: Umeå University
• Contact: Camilla Sandberg
• Phone: +46730395773
• Email: camilla.sandberg[@]umu.se
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Aim: to evaluate the effect of muscle strengthening exercise training in adults with Fontan circulation compared to healthy controls. Hypothesis: adults with Fontan circulation have a relatively lower effect of muscle strengthening exercise training compared to healthy controls.

Description:

10 adults with Fontan circulation will be recruited from the clinic specialised in adults with congenital heart disease at Norrlands Universitetssjukhus. In addition, 10 age- and sex matched controls will be recruited. The sample size is estimated according to a previous study with the same primary outcome. We estimate that 7 patients and 7 controls are needed in the study and plan to enrol 10 patients and 10 controls in case of any drop outs. Muscle tests will be performed at baseline. Based on the results from the muscle tests, an individualised muscle training exercise protocol will be designed and the participants will be working out at a gym during 10 weeks. After 10 weeks the same tests will be performed to evaluate the effect of the muscle training exercise. In addition to the muscle tests, muscle mass and aerobic exercise capacity will be evaluated with peripheral quantitative computed tomography and cardiopulmonary exercise test respectively. Physical activity will be mapped with a validated questionnaire (IPAQ) and an accelerometer attached to the participants thigh. Any impact on fatigue will be evaluated with a validated questionnaire (MFI-20). All tests and questionnaires will be performed at baseline and at follow-up.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. completion date: November 30, 2023
• Est. primary completion date: November 30, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age minimum 18 years
• Patients: Congenital heart disease (Fontan circulation, univentricle heart)
• Controls: no known congenital heart disease.

Exclusion Criteria:

• Muscle strenghtening exercise training at regular basis (2 times/week or more)
• Active disease or other condition that affect exercise training (e.g. rheumatoid arthritis)
• Cognitive or psychological affection
• Other conditions that affect independent decision-making competence

Related Conditions & MeSH terms

• Congenital Heart Disease
• Heart Defects, Congenital
• Heart Diseases
• Univentricular Heart

Intervention

Other:
• Individualised muscle strengthening exercise training protocol.
Based on the results of muscle function tests at baseline an individualised exercise protocol will be designed.

Locations

Country	Name	City	State
Sweden	Umeå University Hospital	Umeå

Sponsors (1)

Lead Sponsor	Collaborator
Umeå University

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in muscle oxygenation kinetics evaluated with near-infrared spectroscopy (NIRS).	Muscle oxygenation kinetics will be evaluated with near-infrared spectroscopy (NIRS) (PortaLite mini, Artinis medical system BV, Netherlands). With light in the near infrared spectra it is possible to measure oxygenated and deoxygenated haemoglobin within the muscle. the muscle oxygenation kinetics till be evaluated pre, during and post exercise of muscle endurance in shoulder flexion and heel raise.	10 weeks
Secondary	Change of isometric muscle strength	Isometric muscle strength in elbow flexion and knee extension will be assessed with a load cell amplifier (VZ101BH 500kg, Anyload Weigh & Measure Inc.,NJ, US). Maximal muscle contraction will be performed during five seconds. The test is repeated three times with a one-minute rest in between. Isometric grip strength will be assessed with a handheld dynamometer (JAMAR, Lafayette, IN, USA). The handle is pressed during three seconds and the test is repeated three times, with a one-minute rest in between. The tests are performed at baseline and at follow up after 10 weeks muscle training exercise protocol.	10 weeks
Secondary	Change of muscular endurance	Muscle endurance in shoulder flexion will be assessed with a dumbbell (women 2 kg, men 3 kg) and performed in pace with a metronome, 20 contractions per minute (40 beats per minute). Muscle endurance in the calf muscles will be assessed with heel raise with 10 degrees dorsal flexion in the ankle. The test is performed in pace with a metronome with 30 contractions per minute (60 beats per minute). To evaluate muscle endurance in elbow flexion and knee extension, the test person lifts a weight representing 80% of repetition maximum measured at isometric strength. During all tests, the test person performs as many contractions as possible.	10 weeks
Secondary	Change of muscle mass	Evaluation of muscle mass and muscle density is performed with peripheral quantitative computed tomography (PQCT) which analyse cross section of under arms and lower legs with a low radiation dose (0.01 mSV).	10 weeks
Secondary	Change of aerobic exercise capacity	Cardiopulmonary exercise tests (CPET) are performed according to standardised protocols with incremental increase of workload. During CPET oxygen and carbon dioxide is measured continuously in the inhaled and exhaled air. Peak watt and peak oxygen uptake capacity (peak VO2) is noted. CPET is used to evaluate the effect of muscle strengthening exercise on the aerobic capacity.	10 weeks