A Virtually Delivered Exercise Intervention To Mitigate Cognitive Deficits From Radiotherapy In AYAs With Brain Tumors

Description

To test a new investigational virtual exercise program for adolescents and young adults (AYAs) with brain tumors who plan to receive cranial radiotherapy

Conditions

Brain Tumor, Brain Cancer

Study Overview

Study Details

Study overview

To test a new investigational virtual exercise program for adolescents and young adults (AYAs) with brain tumors who plan to receive cranial radiotherapy

A Virtually Delivered Exercise Intervention To Mitigate Cognitive Deficits From Radiotherapy In AYAs With Brain Tumors

A Virtually Delivered Exercise Intervention To Mitigate Cognitive Deficits From Radiotherapy In AYAs With Brain Tumors

Condition
Brain Tumor
Intervention / Treatment

-

Contacts and Locations

Houston

M D Anderson Cancer Center, Houston, Texas, United States, 77030

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Age 15-39 years old
  • 2. Self-reported diagnosis of a primary benign or malignant brain tumor or confirmed diagnosis of primary benign or malignant brain tumor radiographically or pathologically when available (relapse or newly diagnosed)
  • 3. Plans to receive CRT at MDACC or, if the participant has already started CRT, the participant is eligible if they are within 3 weeks of the start of CRT
  • 4. Received appropriate physician clearance
  • 5. Able to move arms and legs, and ambulate safely
  • 6. Participant is insufficiently active (reports less than 150 minutes of planned moderate-vigorous intensity activity per week in the prior week)
  • 7. Participants and/or guardians are willing and able to provide informed consent
  • 8. Has a smartphone with available space to download additional apps
  • 9. Does not have sensorimotor strip impairment as indicated by the clinical team
  • 10. Has internet access
  • 11. Can receive physical therapy because this is part of the standard of care
  • 12. Participants and/or guardians are willing and able to provide informed consent for protocol PA18-0130 (Pediatric Energy Balance Data Repository Study), companion protocol for the Fitbit application/assessment.
  • 1. Non-English speaking
  • 2. Screen failure for exercise safety based on Physical Activity Readiness Questionnaire (PAR-Q).12
  • 3. Underlying unstable cardiac or pulmonary disease or symptomatic cardiac disease
  • 4. Recent fracture or acute musculoskeletal injury that precludes ability to participate in supervised exercise training sessions
  • 5. Cognitive and/or major sensory deficits that would impede the completion of research activities and assessments as deemed by the clinical team.
  • 6. Self-reported diagnosis of a metastatic brain tumor or confirmed diagnosis of a metastatic brain tumor radiographically or pathologically when available
  • 7. Self-report of pregnancy
  • 8. Currently enrolled in another physical activity or exercise intervention
  • 9. Prisoners
  • 10. Self-reported pregnancy status

Ages Eligible for Study

15 Years to 39 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

M.D. Anderson Cancer Center,

Maria Swartz, MD, PRINCIPAL_INVESTIGATOR, M.D. Anderson Cancer Center

Study Record Dates

2027-02-28