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Effect of A Multimodal Exercise Intervention on Chemotherapy Uptake in Newly Diagnosed Pediatric and AYA Sarcoma Patients
Recruiting
Effect of A Multimodal Exercise Intervention on Chemotherapy Uptake in Newly Diagnosed Pediatric and AYA Sarcoma Patients (ACTIVE-SARC)
Who can join
Ages 12 to 39 · All sexes
Full eligibility criteria
Inclusion Criteria: 1. Diagnosis of Sarcoma 2. Pediatric or AYA (12-39 years old) 3. Able to provide written informed consent 4. Able to speak, read, and understand English or Spanish 5. Initiating first-line systemic therapy (Doxorubicin, Ifosfamide, Gemcitabine, Docetaxel, Trabectedin, Vincristine, Irinotecan, Temozolomide, Topotecan, Etoposide, Dacarbazine, Pazopanib, Tazemetostat, Imatinib, Sunitinib, Pembrolizumab, Nivolumab, Ipilumumab, Regorafenib, Atezulimumab). Participants can be enrolled up to 90 days after starting firstline systemic therapy. 6. Approval from a medical oncology provider to participate. 7. Having not consistently (not equal to or more than 50% of the time) engaged in more than 90 minutes of moderate or 45 minutes of vigorous physical activity per week over the past 3 months 8. Having not consistently engaged in resistance training 2 or more days per week over the past 3 months Exclusion Criteria: 1. \< 12 or \>39 years old 2. Unable to provide consent 3. Unable to read or understand English or Spanish 4. Oxygen-dependent 5. Unable to walk 2 blocks without assistance (excluding canes) 6. Unstable bone metastases 7. More than 90 days from initiation of first-line systemic therapy. 8. Presence of a severe medical condition or psychiatric condition or medications that would preclude participation of the study intervention, as determined by the patient's provider and study clinician.
About the study
The purpose of this study is to determine the effects of a multimodal exercise intervention on chemotherapy uptake in newly diagnosed pediatric, adolescent and young adult (AYA) Sarcoma patients.
What is being tested
- Exercise Intervention (behavioral)
- Usual Care Control (behavioral)
- Exit Interview (behavioral)
Sponsor: University of Miami · Participants: 40 · Started: Feb 5, 2026
Contact the study team
- Grey Freylersythe, BS · Phone: 305-243-9832
Official record on ClinicalTrials.gov — NCT07359911
Locations in the U.S.
| Florida | University of Miami, Miami |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.