Adjunctive Bright Light Therapy for Opioid Use Disorder
Completed · Not applicable · Has a placebo group
Conditions studied: Opioid Use Disorder, Sleep Disturbance
In brief
Investigators propose to conduct a pilot double-blind, parallel arm, randomized placebo-controlled trial evaluating the feasibility, acceptability, and preliminary efficacy of bright light therapy on reward system functioning among patients undergoing medication-assisted treatment for opioid use disorder.
Key facts
- Study ID
- NCT05459922
- Run by
- Arizona State University
- People needed
- 23
- Starts
- 2022-10-23
- Expected to finish
- 2026-02-11
- Last updated by the study team
- 2026-07-24
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- age between 18 and 65
- ability to speak, write, and read in English
- past 2 weeks of insomnia as evidenced by Insomnia Severity Index (ISI) total score of ≥10
- enrolled in outpatient medication-assisted treatment for OUD (i.e., either methadone or buprenorphine treatment)
- been in medication-assisted treatment for at least 3 months
- at least one month of stable methadone or buprenorphine dose
- have a smartphone
You may not qualify if…
- lifetime history of bipolar disorder or mania
- current narcolepsy, sleep paralysis, or restless leg syndrome as assessed by medical history
- history of seizure disorders/epilepsy
- the STOP-Bang score for obstructive sleep apnea ≥ 5
- retinal pathology, history of eye surgery or taking photosensitizing medications (e.g., lithium, L-tryptophan)
- current regular use of melatonin
- have circumstances that would interfere with study participation (e.g., impending jail sentence)
- previous experience with bright light therapy
- working a night shift or traveling outside the Arizona time zone in the past month
- pregnant, trying to get pregnant, or breastfeeding
- currently wearing prescription glasses with blue-light protection
Where it is running
- Arizona State University — Phoenix, Arizona, United States
Full record on ClinicalTrials.gov
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