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Morning Bright Light to Improve Sleep Quality in Veterans

Morning Bright Light to Improve Sleep Quality in Veterans

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03578003
Enrollment
200
Registered
2018-07-05
Start date
2017-08-02
Completion date
2026-12-01
Last updated
2025-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Injuries, Traumatic, Post-traumatic Stress Disorder

Keywords

Sleep, Bright Light

Brief summary

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.

Interventions

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

Sponsors

Oregon Health and Science University
CollaboratorOTHER
Portland VA Medical Center
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Veterans

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Change in Insomnia Severity Index (ISI)Baseline; after 4 weeks of intervention; and 2 months after the end of interventionMeasures self-reported insomnia severity; total score range = 0-28 (higher total score = worse insomnia)

Countries

United States

Contacts

Primary ContactMiranda M Lim, MD, PhD
lmir@ohsu.edu503-220-8262
Backup ContactJonathan E Elliott, PhD
elliojon@ohsu.edu503-220-8262

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026