Exercise Training and NR Supplementation Trial to Improve Fitness in AYA HCT Survivors

Recruiting Phase 2 Interventional Study
Lymphoblastic Leukemia Cancer Survivors Aplastic Anemia Myelodysplastic Syndromes Myeloid Leukemia
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
10 – 30
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
80 (estimated)
Sponsor
Children's Hospital of Philadelphia · Other
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About This Trial
This will be a randomized, placebo-controlled trial with a 2x2 factorial design testing the effects of an NAD+ precursor (NR) and exercise on skeletal muscle quality and VO2max in AYA HCT survivors. The primary outcome is the change in muscle strength (isometric knee extension) from baseline to 16 weeks. Key secondary outcomes are the change in muscle strength (ankle plantarflexion) from baseline…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Males and females, ages 10-30 years at enrollment 2. Able to understand and speak English 3. Diagnosis of leukemia (myeloid, lymphoid), aplastic anemia, bone marrow failure syndrome, or myelodysplastic syndrome requiring allogeneic HCT 4. 6-48 months from allogeneic HCT 5. Fe…
Contacts

Katherine Cambareri, MPH

445-942-7801

cambarerik@chop.edu

CONTACT

Kristin Wade

267-398-5761

wadekl@chop.edu

CONTACT