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



Status:Active, not recruiting
Conditions:Back Pain, Back Pain
Therapuetic Areas:Musculoskeletal
Healthy:No
Age Range:18 - 70
Updated:3/28/2019
Start Date:August 2014
End Date:December 2019

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Nearly 50% of U.S. veterans report they experience pain on a regular basis. This chronic pain
often co-occurs with other disorders including post-traumatic stress disorder (PTSD),
depression, anxiety and insomnia. A common approach to treating chronic pain is opioid
analgesics, which are not always effective, and increasingly associated with abuse and
misuse. Thus, there is an urgent need to develop readily available, safe, and practical
complementary nonpharmacological approaches to manage chronic pain in U.S. veterans. Chronic
pain is a multidimensional phenomenon, inter-related with many factors, including negative
mood and poor sleep. The central circadian clock, in the suprachiasmatic nucleus in the
hypothalamus, is well recognized to regulate both mood and sleep, and even small delays
(shifts later) in circadian/sleep timing are associated with depression and disrupted sleep.
These results suggests that later circadian/sleep timing may be a modifiable risk factor for
pain. Thus, a self-administered morning bright light treatment at home may be a potentially
efficacious adjunctive strategy for managing chronic pain. This R34 grant will develop a
morning bright light treatment to help manage chronic pain and improve PTSD symptoms,
depression, anxiety and sleep in U.S. veterans. Patients will have 7 baseline days at home,
followed by a baseline pain sensitivity assessment and 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 circadian phase. Assessments will be repeated after another 7 days of morning
bright light treatment. Pain, mood and sleep (wrist actigraphy) will be assessed daily
throughout baseline and treatment. Pain, mood and sleep will also be rated by veterans daily
during a 1 month follow up after cessation of light treatment. This study will determine the
feasibility, acceptability and efficacy of bright light treatment in a sample of U.S.
veterans experiencing chronic low back pain.


Inclusion Criteria:

1. U.S. veteran

2. musculoskeletal pain of the lower back and/or leg pain stemming from degenerative disk
disease, spinal stenosis, or disk herniation (radiculopathy subcategory), or muscular
or ligamentous strain (chronic myofascial pain subcategory) verified with written
confirmation from physician/medical record

3. age between 18 and 70 years

4. live within 1.5 hours drive of Rush University Medical Center

Exclusion Criteria:

1. inability to understand English well enough to complete questionnaires or to
participate;

2. unable to travel to the lab
We found this trial at
1
site
1653 W. Congress Parkway
Chicago, Illinois 60612
(312) 942-5000
Principal Investigator: John W Burns, PhD
Phone: 312-563-4785
Rush University Medical Center Rush University Medical Center encompasses a 664-bed hospital serving adults and...
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Chicago, IL
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