Congenital Heart Disease
Conditions
Keywords
Child, Adult
Brief summary
The overall goal of this program is to create a remote, mobile application enabled exercise program for patients with Congenital Heart Disease (CHD). Pilot trials will consist of a remote exercise program with app-embedded exercise modules designed to promote and encourage safe and healthy exercise habits across a range of CHD anatomies. This app-enabled program will allow for real time data collection integrating wearable devices, as well as compliance and safety monitoring to enhance research capabilities. The app-enabled program will be versatile and may be applied in the future to patients with non-cardiac conditions.
Interventions
BEHAVIORALStrong Hearts Exercise Program
The participant will either begin at the easiest variation of each strength exercise (level A), or will be placed at a specific level for each strength exercise based on their assessment with physical therapy. Participants can progress to the next level of difficulty of a specific strength exercise based on their rating of perceived exertion (RPE) with the opportunity to move to the next level if they have RPE score of 6 or less and if their heart rates are at goal. Each participant will be provided with heart rate ranges based on the heart rate reserve (HRR) method using their baseline resting and peak heart rates obtained during their cardiopulmonary exercise testing (CPET) or percent predicted heart rate based on age if CPET is not available. HRR goals will be set individually for patients and adjusted per protocol to guide effort.
Sponsors
Duke University
Food and Drug Administration (FDA)
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
10 Years to 50 Years
Healthy volunteers
No
Inclusion criteria
* Repaired or unrepaired Congenital Heart Disease (CHD) * Between ages 10 and 50, inclusive, at time of consent * Android or Apple smartphone that meets the operating systems below with the ability to download applications from either Google Play or the Apple store * Android: 6.0 or higher * Apple: iPhone Operating System (iOS) 13 or higher
Exclusion criteria
* Physical or mental disabilities preventing exercise participation * Uncontrolled systemic hypertension (symptomatic or greater than Stage 2 hypertension while on therapy) * Poorly controlled arrhythmia * Clinically unstable heart failure * Known pregnancy at the time of enrollment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in peak rate of oxygen volume consumption (VO2) on Cardiopulmonary Exercise Testing | Baseline, up to 12 weeks |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Pediatric Cardiac Quality of Life Inventory | 1 year | The Pediatric Cardiac Quality of Life Inventory generates 3 scores (total, disease impact subscale, and psychosocial impact subscale). Each subscale has a maximum of 50 points and their sums yields the total score. Higher scores indicate better perceived health-related quality of life. |
| Change in Short Form 36 (SF-36) Health Survey | 1 year | The Short Form 36 Health Survey consists of 8 subscales (physical functioning, role limitations due to physical health, role limitations due to emotional problems, energy/fatigue, emotional well-being, social functioning, pain, and general health). The survey will be scored using the two step RAND scoring process. The first step scores each question on a scale from 0 (worst) to 100 (best) and represents the percentage of total possible score achieved. The second scoring step, takes the average of all the questions in each subscale to create the 8 scores. |
| Change in sit-to-stand test | Baseline, up to 12 weeks | — |
| Change in secondary Cardiopulmonary Exercise Testing outcome measures | Baseline, up to 12 weeks | — |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORReid C Chamberlain, MD, MSCI
Duke UMC
Outcome results
None listed