Skip to main content
OpenTrials
Recruiting

NCT Number: NCT03578003

Morning Bright Light to Improve Sleep Quality in Veterans

One of the principal complicating factors associated with traumatic brain injury (TBI) is sleep-wake disturbances (e.g., insomnia, excessive daytime sleepiness, and circadian rhythm sleep disorders). Morning bright light therapy (MBLT) has been shown to improve sleep quality in a variety of conditions, but little has been done investigating the utility of MBLT in improving sleep in Veterans with TBI. This proposal aims to determine the effect of MBLT on sleep quality in Veterans with TBI. Veterans with and without TBI will be recruited from the VA Portland Health Care System. Baseline questionnaires and 7 days of actigraphy will be collected prior to engaging in 60 minutes of MBLT daily for 4 weeks, during which actigraphy will also be collected continuously. Post-MBLT questionnaire data will be collected, and follow-up questionnaire data will be collected at 3 months post-MBLT.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

VA Portland Health Care System

Portand, Oregon, 97239, United States

Location status: Recruiting

Location contact

Miranda M Lim, MD, PhD

CONTACT

[email protected]

503-220-8262 ext. 57404

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Veterans

Exclusion criteria

  • History of bipolar disorder
  • History of macular degeneration
  • Non-English speaking
  • Decisionally impaired
  • Currently using a light box

Treatment and study plan

Morning Bright Light Therapy

Other

60 minutes of bright light therapy (10,000 lux) received within 90 minutes of waking

Primary outcomes

  1. Change in Insomnia Severity Index (ISI)

    Time frame: Baseline; after 4 weeks of intervention; and 2 months after the end of intervention

    Measures self-reported insomnia severity; total score range = 0-28 (higher total score = worse insomnia)

Study contacts

Contact information is provided by the study sponsor or research team.

Jonathan E Elliott, PhD

CONTACT

[email protected]

503-220-8262 ext. 58020

Miranda M Lim, MD, PhD

CONTACT

[email protected]

503-220-8262 ext. 57404

Sponsors and collaborators

Lead sponsor

Portland VA Medical Center

Fed

Collaborators

  • Oregon Health and Science University

Registry information

Important dates

Study start
2017
Primary completion
2026
Study completion
2026
First posted
Jul 5, 2018
Registry last updated
Nov 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.