ClinicalTrials.gg
RecruitingNCT06720090KLTOUpdated Aug 18, 2026

Light Therapy for Obsessive-compulsive Disorder (OCD)

An Early Phase 1 interventional study of Light therapy in OCD, sponsored by Washington University School of Medicine. Recruiting at 1 site in United States. Open to participants aged 17 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-18.

Sponsored by Washington University School of Medicine · Early Phase 1, Interventional, and Treatment

From the registry’s dates

  • Started Dec 2024; still recruiting 1 year 10 months later.
Phase
Early Phase 1
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
17 Years to 35 Years
Sex
All
01

Study summary

The goal of this clinical trial is to test whether light therapy is effective for reducing symptoms in young adults with OCD and late bedtimes (1am or later). The main question[s] it aims to answer are:

Does light therapy reduce OCD symptoms? Does light therapy advance the circadian clock? If there is a comparison group: Researchers will compare a higher dose of light therapy to a lower dose to see if dose amount affects symptom reduction.

Participants will asked to:

  1. Wear light therapy glasses for 1 hour each morning and complete a daily light therapy log for 5 weeks
  2. Track their sleep every day with a wearable monitor and an electronic sleep diary for 5 weeks
  3. Complete a 1-time assessment of sensitivity to light exposure
  4. Complete self-report measures of OCD 4 times/day at baseline (2 weeks), mid-treatment (1 week), and end of treatment (1 week)
02

Conditions studied

  • OCD

Keywords

  • ocd
  • sleep
  • light therapy
  • circadian
  • behavioral treatment
03

In context

Lead sponsor

Washington University School of Medicine is the lead sponsor of 1,803 studies on the registry; 271 are open to participants now.

Of its 329 completed or terminated interventional studies of FDA-regulated products, 216 (66%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
17 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Primary OCD diagnosis
  2. Bedtime 0100 or later
  3. Age 18-35
  4. English speaking

Exclusion criteria

Exclusion Criteria:

  1. Subjects must not be currently participating in another research study that would influence their participation in our study.
  2. Diagnostic status
  3. Treatment status
  4. Night shift work or travel more than 1 time zone outside of Central Standard Time (CST) in the past month
  5. Pregnancy status
  6. Medication status
  7. Regular nicotine or marijuana use
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

DSM diagnostic criteria

The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.

05

Study design

Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Higher dose

    Participants will be given wearable light therapy devices that emit a higher light intensity.

    Behavioral: Light therapy

  • Sham comparator
    Lower dose

    Participants will be given wearable light therapy devices that emit a lower light intensity.

    Behavioral: Light therapy

Interventions

  • BehavioralLight therapy

    5 weeks of light therapy administered via wearable light therapy glasses worn for 1 hour each morning after awakening.

06

What researchers measure

Primary outcomes

  1. Yale Brown Obsessive-Compulsive Scale (YBOCS)

    A retrospective clinical interview of OCD symptom severity. Score range from 0 to 40 and higher scores indicate more severe OCD symptoms.

    Time frame: Administered at baseline, in treatment week 3, and post-treatment (3 administrations over 7 weeks)

  2. Daily Perseverative Thinking Questionnaire

    Self-report measure of momentary transdiagnostic repetitive negative thinking. Score range from 6 to 42 and higher scores indicate more severe repetitive negative thinking.

    Time frame: Administered 4 times/day for 2 weeks at baseline, 4 times/day for 1 week in treatment week 3, and 4 times/day for 1 week in treatment week 5

Secondary outcomes

  1. Circadian melatonin phase

    Dim light melatonin onset assessed by taking hourly saliva samples in dim light conditions for 10 hours beginning 7 hours before typical bedtime and ending 2 hours after typical bedtime.

    Time frame: At baseline and post-treatment (after 5 weeks of treament)

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Dec 2024 (actual). Primary completion is estimated for Mar 2029, 51 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 21, 2024
First posted
Dec 6, 2024
StartActual
Dec 16, 2024
Primary completionEst.
Mar 2029
CompletionEst.
Mar 2029
Last update
Aug 18, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06720090
Responsible party
Rebecca C. Cox (Assistant Professor, Washington University School of Medicine) — Principal investigator
First posted
Dec 6, 2024
Start date
Dec 16, 2024
Primary completion
Mar 2029 (estimated)
Completion
Mar 2029 (estimated)
Last update
Aug 18, 2026

Study contacts

Rebecca Cox, BA
Contact
scraplab@wustl.edu
314-935-8111
Rebecca Cox, PhD
principal investigator · Washington University School of Medicine

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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