Adult Soft Tissue Sarcoma Clinical Trials

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

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Maximum Age: 39
Healthy Volunteers: f
View:

• 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

Locations
United States
Florida
University of Miami
RECRUITING
Miami
Contact Information
Primary
Grey Freylersythe, BS
g.freylersythe@med.miami.edu
305-243-9832
Backup
Loren Yavelberg, PhD
l.yavelberg@med.miami.edu
Time Frame
Start Date: 2026-02-05
Estimated Completion Date: 2027-08-05
Participants
Target number of participants: 40
Treatments
Experimental: Exercise Intervention Group (EXE)
Participants in this group will undergo supervised multimodal (aerobic, resistance, balance) moderate-to-vigorous exercise intervention three 3 times per week for 12 weeks, a total of 36 sessions.~Total participation duration is about 12 weeks.
Other: Usual Care Control Group (UC)
Participants in this group may opt to receive a weekly brief symptom self-assessment as a survey.~Total participation duration is about 12 weeks.
Related Therapeutic Areas
Sponsors
Collaborators: Florida Department of Health
Leads: University of Miami

This content was sourced from clinicaltrials.gov