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NCT07359911Recruiting

Effect of A Multimodal Exercise Intervention on Chemotherapy Uptake in Newly Diagnosed Pediatric and AYA Sarcoma Patients

Effect of A Multimodal Exercise Intervention on Chemotherapy Uptake in Newly Diagnosed Pediatric and AYA Sarcoma Patients (ACTIVE-SARC)

Source: ClinicalTrials.gov · Last updated 18 Feb 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
14 Jan 2026
Start date
5 Feb 2026
Primary completion date
5 Aug 2027
Lead sponsor
University of Miami
NCT number
NCT07359911

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 5 Feb 2026 to the primary completion date, 5 Aug 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • More than 90 days from initiation of first-line systemic therapy.

Other illness

  • 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.

Age

  • \< 12 or \>39 years old

Other

  • Unable to provide consent
  • Unable to read or understand English or Spanish
  • Oxygen-dependent
  • Unable to walk 2 blocks without assistance (excluding canes)
  • Unstable bone metastases

Who the study is looking for

  • Diagnosis of Sarcoma
  • Pediatric or AYA (12-39 years old)
  • Able to provide written informed consent
  • Able to speak, read, and understand English or Spanish
  • 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.
  • Approval from a medical oncology provider to participate.
  • 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
  • Having not consistently engaged in resistance training 2 or more days per week over the past 3 months

Age in the registry: 12 years to 39 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Miami
Coordinator of this site? Confirm its status
MiamiUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.