Actively Recruiting

Phase Not Applicable
Age: 18Years - 89Years
All Genders
NCT06477796

Improving Sleep in Veterans With the Polytrauma Clinical Triad

Led by VA Office of Research and Development · Updated on 2025-06-27

96

Participants Needed

1

Research Sites

178 weeks

Total Duration

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AI-Summary

What this Trial Is About

The "polytrauma clinical triad" (PCT), a highly disabling constellation of factors, is defined by the coexistence of traumatic brain injury, post-traumatic stress disorder, and chronic pain. Veterans with the PCT are medically complex, often refractory to conventional therapies, and suffer from additional related chronic sequela. Notably, sleep disturbances and cognitive impairment, which the investigators hypothesize are significant contributing factors to these functional impairments and an impediment toward rehabilitation. Thus, the investigators' research aims to intervene "at the level of sleep", and by improving sleep, improve these interconnected, disabling, and difficult to treat enduring complexities associated with the PCT - ultimately to improve Veteran quality of life, functional independence, and restorative function. The investigators predict that the proposed intervention, morning bright light therapy, which is cost-effective, rapidly deployable and home-based, will be effective in improving sleep and overall PCT symptom management, thereby, resulting in a measurable and impactful improvement in quality of life.

CONDITIONS

Official Title

Improving Sleep in Veterans With the Polytrauma Clinical Triad

Who Can Participate

Age: 18Years - 89Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Veteran
  • English speaking with phone and internet access
  • Current self-reported sleep disturbances
  • Clinically stable for current pharmacologic or behavioral health treatments for depression, anxiety, sleep and pain
  • Documented history of traumatic brain injury
Not Eligible

You will not qualify if you...

  • Decisional impairment and/or dementia
  • Current usage of a lightbox or negative ion generator
  • Shift work
  • History of macular degeneration and/or bipolar disorder
  • Evidence for suicidal ideation
  • Cancer diagnosis within the past 6 months
  • Surgery within the past 6 months
  • Substance abuse within the past 6-12 months
  • Significant impairing post-stroke residual hemiparesis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

VA Portland Health Care System, Portland, OR

Portland, Oregon, United States, 97207-2964

Actively Recruiting

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Research Team

J

Jonathan E Elliott, PhD

CONTACT

J

Joshua P Kreider

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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