Sleep Disorders Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You were diagnosed with a brain tumor and received treatment at Texas Children's Hospital
- Your treatment included surgery alone, or surgery combined with proton beam radiation therapy
- Your brain tumor was not one of the following types: high-grade glioma, brain stem glioma, or atypical teratoid rhabdoid tumor
- You are currently or were previously part of a long-term study looking at thinking and learning skills in childhood brain tumor survivors at Texas Children's Hospital (confirm with trial site)
- You are between 10 and 18 years old
- It has been at least 1 year since your brain tumor diagnosis
- You experience mild to moderate levels of fatigue, as measured by a specific questionnaire called the PROMIS
- A provider from a Long-Term Survivorship program has approved your participation
- You have good enough vision to use a computer for tasks in the study
- You speak English
- Your IQ score is above 70
Who may not be able to join:
- You have been diagnosed with or treated for a new cancer in the past 12 months
- You have had thoughts of suicide or severe depression requiring urgent care either currently or within the past 12 months
- You have sensitivity to light, another eye condition, seizures, or migraines
- You currently take medications that make your skin or eyes more sensitive to light
- You have used light therapy before or are currently using it
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Kimberly P Raghubar, PhD, Baylor College of Medicine
Phone: 832-822-3713
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Percent of approached participants who consent to study participation; Percent of sessions completed during all 6 weeks of bright or dim light exposure; Percent of participants rating the intervention as acceptable by indicating that they would recommend this intervention to other survivors.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.