Actively Recruiting
Light Therapy to Improve Sleep in Veterans With Traumatic Brain Injury: Sleep-active Biomarkers and Glymphatic Function
Led by Oregon Health and Science University · Updated on 2026-05-22
300
Participants Needed
1
Research Sites
93 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating how improving sleep through morning bright light therapy can affect important brain health processes such as mitochondrial function, systemic inflammation, and glymphatic function in people with traumatic brain injury (TBI). This study aims to better understand these biological changes related to sleep improvement. The research is led by Oregon Health and Science University and uses approved methods for safety and consistency. The trial compares two treatments: one group receives morning bright light therapy, involving exposure to bright light for one hour each morning over four weeks. The other group receives negative ion generator therapy under the same schedule. Both interventions are delivered daily in the morning, and participants are randomly assigned to one of these two groups. The study is single-masked, meaning participants know their treatment but certain staff may not. Participants will be monitored before and after the four-week treatment period through blood tests measuring inflammation markers and mitochondrial function, as well as advanced MRI scans assessing glymphatic system function. The study requires participants to have stable clinical status and sleep disturbances related to TBI. Safety screenings include MRI compatibility and pregnancy tests. The total participation time includes baseline assessments, the treatment period, and post-treatment evaluations to track changes in these key brain health indicators.
CONDITIONS
Brief Title
Light Therapy to Improve Sleep in TBI: Sleep-active Biomarkers and Glymphatic Function
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male and female; any race; 18-89 years of age
- English speaking
- Accessible via phone
- Non-decisionally impaired, able to understand and verbalize the study protocol
- Documented history of traumatic brain injury (TBI) per VA/DoD guidelines
- Self-reported sleep-wake disturbances
- Clinically stable on current treatments for depression, anxiety, sleep, and pain
- MRI compatible with no disqualifying implants or conditions
- Able to lie flat on back without thick pillow for extended MRI scanning
- Shoulder width fits within MRI safety limits
You will not qualify if you...
- History of macular degeneration
- History of bipolar disorder
- Current use of a lightbox or negative ion generator
- Shift work employment
- MRI contraindications including pacemaker, metal implants, aneurysm clips
- History of claustrophobia or inability to tolerate MRI
- Pregnancy, breastfeeding, or implanted IUD
- History of non-removable hearing aids, middle/inner ear prosthesis, or dentures
- History of head surgery with aneurysm clips
- Eye metal exposure without negative screening
- Unable to communicate in English
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 4 weeks
Participants receive exposure to either bright light or negative ions shortly after waking every day for an hour.
Daily sessions for 4 weeks
Trial Site Locations
Total: 1 location
1
Oregon Health and Science University
Portland, Oregon, United States, 97239
Actively Recruiting
Research Team
J
Jonathan Elliott, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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