Exercise Clinical Trial
Official title:
Vasodilators and Exercise as Adjuvant Therapy for Duchenne Muscular Dystrophy (VASO-REx Study)
Examining two strategies as potential adjuvant therapies for Duchenne muscular dystrophy (DMD); aerobic exercise training (to induce adaptations in skeletal muscle and improve cardiovascular health) and tadalafil, an FDA-approved vasodilator (to optimize blood flow and muscle perfusion which is impaired and often overlooked in DMD). Target: improved muscle function, vascular health, and DMD treatment.
Status | Not yet recruiting |
Enrollment | 50 |
Est. completion date | November 2026 |
Est. primary completion date | November 2026 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 6 Years and older |
Eligibility | Inclusion Criteria: - Diagnosis of DMD confirmed by genetic report - Minimum entry age of 6.0 years old - Ambulatory - On stable glucocorticoid regimen (for > 3 months) Exclusion Criteria: - Contraindication to a Magnetic resonance Imaging examination (e.g. severe claustrophobia, magnetic implants, unable/unwilling to perform test) - Presence of unstable medical problems, including severe cardiomyopathy, left ventricular ejection fraction <45%, cardiac conduction abnormalities as evidenced on ECG, uncontrolled seizure disorder, uncontrolled hypo or hypertension - Presence of a secondary condition that impacts muscle function or muscle metabolism (e.g., myasthenia gravis, endocrine disorder, mitochondrial disease) - Presence of a secondary condition leading to developmental delay or impaired motor control (e.g., cerebral palsy) or previous history of unprovoked rhabdomyolysis - Contraindications to phosphodiesterase 5 inhibitors (use of nitrates, alpha-adrenergic blockers, other phosphodiesterase 5 inhibitors) or other medications known to modulate blood flow or muscle metabolism - Participation in currently approved FDA trials or other investigational clinical trials during the period of the study |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University of Florida | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
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* Note: There are 66 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Vascular responsiveness after muscle contraction to a single dose of tadalafil. | Responsiveness will be determined by an increase in post-contractile muscle oxygenation using MRI-Blood Oxygen Level Dependent (BOLD) responses after dosing compared to before. Study participants demonstrating an increase (>50%) in post-contractile BOLD after tadalafil will be enrolled into Aim 2 of this study. | up to 4 weeks after the completion of Visits 1 and 2 of Aim 1. | |
Primary | Cycling time to fatigue | The study will assess the impact of tadalafil on exercise performance and fatigue resistance compared to placebo. Participants will undergo a maximal effort cycling test before and after the intervention period. The time it takes for participants to reach exhaustion (TTE) will be recorded as the primary outcome measure.
Measurement: Time to exhaustion (TTE) during a maximal effort cycling test on a recumbent, stationary ergometer. This test will quantify fatigue resistance by measuring the duration participants can sustain maximal effort cycling. |
Baseline and 6 month follow-up visits of Aim 2. | |
Secondary | Quadriceps muscle Fat Fraction | This outcome serves as a measure of disease severity. This measure is a sensitive and reproducible biomarker of DMD muscle pathology. | Aim 1 and Aim 2 (baseline and 6 month follow-up) | |
Secondary | Metabolic recovery | The rate of phosphocreatine resynthesis after leg exercise will be quantified and serves as index of skeletal muscle mitochondrial oxidative capacity. (Part of Aim 2 of the study). | Through study completion, an average of 3 years. | |
Secondary | cardiopulmonary exercise testing (CPET) - Peak aerobic capacity (VO2max) | Patients will undergo cycling exercise at submaximal and peak workloads to quantify peak aerobic capacity, ventilation.
Peak Oxygen Uptake (VO2max): This measure quantifies the maximum amount of oxygen the body can utilize during exercise, assessed through maximal cycling effort in a CPET. It serves as a primary indicator of overall cardiovascular and aerobic fitness. Peak aerobic capacity: VO2max reflects the maximum oxygen utilization capacity, indicating overall cardiovascular fitness. |
Through study completion, an average of 3 years. | |
Secondary | cardiopulmonary exercise testing (CPET) - Minute Ventilation (VE) | Minute Ventilation (VE): This measure reflects the total volume of air breathed per minute during exercise, assessed throughout the CPET. Evaluating VE at various workloads provides insights into respiratory efficiency and potential limitations during exercise.
Respiratory efficiency: VE and VE/VO2 assess how well the body utilizes oxygen during exercise, revealing potential respiratory limitations. |
Through study completion, an average of 3 years. | |
Secondary | cardiopulmonary exercise testing (CPET) - Ventilatory Equivalent for Oxygen (VE/VO2) | Ventilatory Equivalent for Oxygen (VE/VO2): This ratio compares ventilation to oxygen uptake, calculated throughout the CPET. It indicates the efficiency of oxygen utilization during exercise and potential respiratory limitations.
Respiratory efficiency: VE and VE/VO2 assess how well the body utilizes oxygen during exercise, revealing potential respiratory limitations. |
Through study completion, an average of 3 years. | |
Secondary | cardiopulmonary exercise testing (CPET) - Gas Exchange Threshold (GET) | Gas Exchange Threshold (GET): This point during exercise marks the transition from predominantly aerobic to anaerobic metabolism, identified through changes in blood lactate levels and other CPET parameters. Analyzing GET helps assess exercise tolerance and potential for improvement.
Exercise tolerance and fatigue: GET and W at AT pinpoint the intensity at which fatigue and performance decline become significant, offering insights into exercise limitations and potential for improvement. |
Through study completion, an average of 3 years. | |
Secondary | cardiopulmonary exercise testing (CPET) - Workload at Anaerobic Threshold (W at AT) | Workload at Anaerobic Threshold (W at AT): This measure, derived from the CPET, quantifies the power output at which anaerobic metabolism significantly contributes to energy production. It reflects exercise intensity at which fatigue and performance decline become prominent.
Exercise tolerance and fatigue: GET and W at AT pinpoint the intensity at which fatigue and performance decline become significant, offering insights into exercise limitations and potential for improvement. |
Through study completion, an average of 3 years. | |
Secondary | The 100-meter timed test (100m) | The 100m is a fixed distance test of maximal performance and will be completed according to published guidelines. | Through study completion, an average of 3 years. | |
Secondary | the North Star Ambulatory Assessment (NSAA) | The North Star Ambulatory Assessment (NSAA) is a 17-item rating scale that is used to measure physical function and motor abilities in ambulatory boys with DMD and is increasingly being used in clinical trials as an overall measure of physical function. | Through study completion, an average of 3 years. | |
Secondary | The 4-stair climb | The time to ascend 4-stairs is a strength-measure. The patient is instructed to climb four standard steps (six inches in height each) with two handrails as fast as safely possible, using the rails if needed. | Through study completion, an average of 3 years. | |
Secondary | The Physical activity questionnaire (PAQ-C) | The PAQ-C is a self-administered, 7-day recall instrument developed to assess general levels of physical activity throughout the elementary school year for students in grades 4 to 8 and approximately 8 to 14 years, with high validity. Although reliability is considered to be moderate, other physical activity questionnaires are less reliable. Results will be correlated with indices of disease severity and tadalafil responsiveness. | Through study completion, an average of 3 years. | |
Secondary | Pulmonary function testing - vital capacity (FVC) | Measurement: FVC, measured using a standard spirometer according to American Thoracic Society guidelines. This is the maximum amount of air an individual can forcefully exhale after a full inhalation.
Significance: FVC reflects the total lung capacity and is a key indicator of overall lung volume and function. It can help identify restrictive lung diseases, where lung volume is limited, and track respiratory health changes over time. |
Through study completion, an average of 3 years. | |
Secondary | Pulmonary function testing - forced expiratory volume in 1 second (FEV1) | Measurement: FEV1, measured using a standard spirometer according to American Thoracic Society guidelines. This is the amount of air forcefully exhaled in the first second of a maximal exhalation after a full inhalation.
Significance: FEV1 reflects the efficiency of airflow from the lungs and is sensitive to obstructive lung diseases, like asthma and Chronic Obstructive Pulmonary Disease (COPD), where airflow is impaired. |
Through study completion, an average of 3 years. | |
Secondary | Neurology Quality of Life (NeuroQoL) pediatric lower extremity function | Questionnaire used to measure patient-reported outcomes of intervention impact. | Through study completion, an average of 3 years. | |
Secondary | Patient Reported Outcomes Measurement Information System (PROMIS) pediatric fatigue | Questionnaire used to measure patient-reported outcomes of intervention impact. | Through study completion, an average of 3 years. | |
Secondary | PROMIS parent proxy for physical activity | Questionnaire used to measure patient's parent-reported outcomes of intervention impact. | Through study completion, an average of 3 years. | |
Secondary | PROMIS pediatric physical activity | Questionnaire used to measure patient's parent-reported outcomes of intervention impact. | Through study completion, an average of 3 years. | |
Secondary | Physical Activity Monitoring - Daily Step Rate | Measurement: Total number of steps taken per day, assessed using the Actigraph activity monitor. | Through study completion, an average of 3 years. | |
Secondary | Physical Activity Monitoring - Time in Low-Level Activity | Measurement: Total time spent in low-intensity physical activity per day, as defined by Actigraph criteria. | Through study completion, an average of 3 years. | |
Secondary | Physical Activity Monitoring - Time in Moderate-Level Activity | Measurement: Total time spent in moderate-intensity physical activity per day, as defined by Actigraph criteria. | Through study completion, an average of 3 years. | |
Secondary | Physical Activity Monitoring - Time in High-Level Activity | Measurement: Total time spent in high-intensity physical activity per day, as defined by Actigraph criteria. | Through study completion, an average of 3 years. |
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