Bright Light Treatment At Home To Manage Chronic Pain In U.S. Veterans

NACompletedINTERVENTIONAL
Enrollment

37

Participants

Timeline

Start Date

August 31, 2014

Primary Completion Date

September 30, 2017

Study Completion Date

February 28, 2018

Conditions
Chronic Low Back Pain
Interventions
DEVICE

Bright light

The purpose of this R34 Pilot and Feasibility study is to develop a morning bright light treatment to help manage chronic pain and improve PTSD symptoms, mood, and sleep in US veterans. Veterans will have 7 baseline days at home, followed by a baseline pain sensitivity assessment and baseline home circadian phase assessment (dim light melatonin onset). Following an instructional home visit, patients will then self-administer morning bright light treatment for 6 days, followed by reassessments of pain sensitivity and home circadian phase. This will be repeated after a further 7 days of morning bright light treatment. The Patient Reported Outcomes Measurement Information System (PROMIS) will also be administered at every lab visit. Additionally, pain and mood (electronic diaries) and sleep (wrist actigraphy) will be assessed daily throughout baseline and treatment. Pain, mood and sleep will also be self-reported daily during a 1 month follow up after cessation of light treatment.

Trial Locations (1)

60612

Rush University Medical Center, Chicago

All Listed Sponsors
collaborator

National Center for Complementary and Integrative Health (NCCIH)

NIH

lead

Rush University Medical Center

OTHER

NCT02373189 - Bright Light Treatment At Home To Manage Chronic Pain In U.S. Veterans | Biotech Hunter | Biotech Hunter