Interval Training in Adults With Congenital Heart Disease a Randomized Trial

Congenital Heart Defects Clinical Trial

Official title:

Effect of Home Based Interval Training on Exercise Capacity and Quality of Life in Adults With Congenital Heart Disease - a Randomized Controlled Multicenter Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01671566
• Other study ID #: GUCHUmU01
• Status: Completed
• Phase: N/A
• First received: August 20, 2012
• Last updated: March 3, 2016
• Start date: September 2012
• Est. completion date: March 2016

Study information

• Verified date: March 2016
• Source: Umeå University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Sweden: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

Adults with congenital heart disease have various degrees of impaired exercise capacity compared to healthy controls. Impaired exercise capacity makes everyday activities more difficult and demanding. There are few studies on effect of exercise training in adults with congenital heart disease. The hypothesis of this study is that structured home based exercise training will improve exercise capacity and health status in the studied population.

Description:

The number adults with congenital heart disease is increasing. Thanks to advances in the medical and surgical fields the number of adults with complex congenital heart disease is now higher than the children with corresponding heart disease. Though the long term prognosis is still unknown and continuously changing as new therapeutic options are introduced.

Persons with congenital heart disease have different degrees of impaired exercise capacity compared to healthy controls. Some studies indicate that this population is not sufficiently active to achieve the recommendations for physical activity in preventing acquired heart disease. Physical inactivity is an important risk factor for developing acquired heart disease and other life style diseases as obesity and diabetes. In a population where one or more previous cardiac surgeries are common, the prevention of life style diseases is especially important. Exercise training in heart failure and coronary artery disease is well studied and there are clinical guidelines. Regarding exercise training in adults with congenital heart disease, however,the information is sparse and further studies are needed.

Based on defined inclusion and exclusion criteria adults with complex congenital heart disease will be recruited in the Northern Health Care Region in Sweden and in Gothenburg. Before and after the twelve week intervention period the investigators will collect information about cardiopulmonary exercise capacity, health related quality of life, exercise self-efficacy, anxiety and depression. The patients will be randomized to twelve weeks of home based interval training or to a control group. The randomization ratio will be 2:1 (intervention:control). The control group will be instructed to continue with their habitual physical activities. The home based interval training program will be individualized based on the results of the exercise tests.

The aim of this study is to examine the effect of home based interval training on maximal and submaximal exercise capacity, quality of life, exercise self-efficacy, anxiety and depression.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 26
• Est. completion date: March 2016
• Est. primary completion date: March 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Complex congenital heart disease (e.g.; Tetralogy of Fallot, Transpositions of the great arteries, Ebstein, Eisenmenger, Pulmonary atresia or Tricuspid atresia)

• Clinically stable without significant change the last 3 months

• Adult (>18 years)

• Informed consent

Exclusion Criteria:

• Signs of arrhythmia on exercise ECG or relevant clinical arrhythmia

• Mental retardation or psychiatric illness affecting the ability of independent decisions

• Other comorbidity affecting physical activity

• Other circumstances making participation unsuitable

• Present strategy of regularly executing physical exercise > 2 times/week in purpose to increase cardiovascular capacity.

• VO2 peak > 30 ml/kg/min

• No access to internet

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor)

Related Conditions & MeSH terms

• Congenital Heart Defects
• Heart Defects, Congenital
• Heart Diseases

Intervention

Behavioral:
• Home based interval training
The participant in the intervention group will receive an individualized interval training program. The individualized adjustments in training load will be made from the results of the CPET-incremental and adjustments in training time from the results of the constant work rate 75% of peak work rate (Watt). The training will be home based and performed on a ergometer cycle 3 times a week for twelve weeks. During exercise they will wear a heart rate monitoring watch. The registered heart rate will be transferred to a webpage after the exercise session. Only the physiotherapist and participant have the access to this page. The physiotherapist and participant will have a weekly contact to promote compliance, provide feedback and if necessary adjust the training time or load. Progression in training load and time will be made when necessary to keep a relevant intensity.

Locations

Country	Name	City	State
Sweden	Sahlgrenska University hospital	Gothenburg
Sweden	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	Peak VO2 (ml/kg/min)	Comparison within and between groups	Before homebased interval exrecise regime and after completion (12 weeks)	No
Primary	Endurance time	at CPET-incremental and constant work rate test at 75% of peak work rate (Watt). Comparison between and within groups.	Before homebased interval exercise regimen and at completion (12 weeks)	No
Secondary	Response during CPET incremental and constant work rate test at 75% of peak work rate (Watt).	(Peak VO2 (l/min) and Iso time, VCO2, VE/VCO2, VE/VCO2-slope, anaerobic threshold, Peak Heart Rate, Heart Rate recovery, Heart Rate response, Peak work rate, Oxygen saturation, Blood pressure, symptoms) Comparison within and between groups.	Before homebased interval exercise regime and at completion (12 weeks)	No
Secondary	Adverse events	Complications to training	Once a week during homebased exercise regime	Yes
Secondary	Quality of life	The EQ-5D and SF 36 questionaires will be used to assess Quality of life. Comparison between and within groups.	Before homebased interval exercise regime and at completion (12 weeks)	No
Secondary	Physical activity level	The long self administered version of International Physical Activity Questionaire (IPAQ) will be used to assess physical activity level. Comparison within and between groups.	Before homebased interval exercise regime and after completion (12 weeks)	No
Secondary	Exercise self-efficacy	The Exercise Self-Efficacy Scale will be used. Comparison within and between groups	Before homebased interval exercise regime and after completion	No
Secondary	Anxiety and depression	The hospital anxiety and depression scale (HAD-scale) will be used to estimate the incidence of anxiety and depression. Comparison between and within groups.	Before homebased interval exercise regime and after completion (12 weeks)	No
Secondary	Response during CPET incremental and constant work rate test at 75 % of peak work rate (Watt).	( Peak VO2 and Iso time(l/min), VCO2, VE/VCO2, VE/VCO-slope, anaerobic threshold, Peak Heart Rate, Heart Rate recovery, Heart rate response, Peak work rate, Oxygen saturation, Blood pressure, symptoms) Comparison within and between groups.	12 months after completion	No
Secondary	Peak VO2( ml/kg/min)	Comparison within and between groups	12 months after completion	No
Secondary	Endurance time	at CPET incremental and constant work rate at 75% of peak work rate (Watt)	12 months after completion	No
Secondary	Quality of life	The EQ-5D and SF 36 questionaires will be used to assess Quality of life. Comparison within and between groups.	12 months after completion	No
Secondary	Physical Activity level	The long self administered version of International Physical Activity Questionaire (IPAQ) will be used to assess physical activity level. Comparison within and between groups.	12 months after completion	No
Secondary	Anxiety and depression	The hospital Anxiety and Depression Scale (HAD-scale) will be used to estimate the incidence of anxiety and depression. Comparison within and between groups.	12 months after completion	No