Actively Recruiting
Cancer-related Fatigue and Its Biological Contributors in Adolescent and Young Adult Brain Tumor Survivors: Effects of a Tele-exercise Intervention
Led by M.D. Anderson Cancer Center · Updated on 2026-03-04
75
Participants Needed
1
Research Sites
329 weeks
Total Duration
On this page
Sponsors
M
M.D. Anderson Cancer Center
Lead Sponsor
C
Cancer Prevention Research Institute of Texas
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this research study is to learn about the effects of the RISE-YA intervention on cancer-related fatigue in young adults who are brain cancer survivors.
CONDITIONS
Official Title
Cancer-related Fatigue and Its Biological Contributors in Adolescent and Young Adult Brain Tumor Survivors: Effects of a Tele-exercise Intervention
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Currently aged 18 to 39 years
- Primary brain tumor diagnosed between ages 15 and 39 years
- Between 6 months and less than 5 years post curative treatment
- Treated with chemotherapy and radiation
- FACIT-Fatigue score of 43 or less
- Engages in less than 150 minutes of physical activity and fewer than 2 muscle strengthening sessions per week
- Able to speak, write, and read English
- No exercise contraindications based on Physical Activity Readiness Questionnaire (PAR-Q+)
- Able to provide informed consent or assent
You will not qualify if you...
- Non-English speaking
- Screen failure for exercise safety
- Unstable or symptomatic cardiac or pulmonary disease
- Recent fracture or acute musculoskeletal injury preventing exercise
- History of chronic disease, secondary cancers, genetic syndromes, or recurrent brain disease needing re-irradiation
- Cognitive or major sensory deficits interfering with research activities
- Pregnancy
- Prisoner status
- Documented developmental disorders or major psychotic illnesses
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of Texas M. D. Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
M
Michael Roth, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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