Actively Recruiting

Phase Not Applicable
Age: 18Years - 89Years
All Genders
ID07601841

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

Age: 18Years - 89Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

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

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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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