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Light Therapy for Obsessive-compulsive Disorder (OCD)

Light Therapy for Obsessive-compulsive Disorder: A Circadian Medicine Approach

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06720090
Acronym
KLTO
Enrollment
40
Registered
2024-12-06
Start date
2024-12-16
Completion date
2029-03-01
Last updated
2026-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

OCD

Keywords

ocd, sleep, light therapy, circadian, behavioral treatment

Brief 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)

Interventions

BEHAVIORALLight therapy

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

Sponsors

Washington University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
17 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

1. Primary DSM-5 OCD diagnosis 2. Bedtime 0100 or later 3. Age 18-35 4. English speaking

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

Design outcomes

Primary

MeasureTime frameDescription
Yale Brown Obsessive-Compulsive Scale (YBOCS)Administered at baseline, in treatment week 3, and post-treatment (3 administrations over 7 weeks)A retrospective clinical interview of OCD symptom severity. Score range from 0 to 40 and higher scores indicate more severe OCD symptoms.
Daily Perseverative Thinking QuestionnaireAdministered 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 5Self-report measure of momentary transdiagnostic repetitive negative thinking. Score range from 6 to 42 and higher scores indicate more severe repetitive negative thinking.

Secondary

MeasureTime frameDescription
Circadian melatonin phaseAt baseline and post-treatment (after 5 weeks of treament)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.

Countries

United States

Contacts

CONTACTRebecca Cox, BA
scraplab@wustl.edu314-935-8111
PRINCIPAL_INVESTIGATORRebecca Cox, PhD

Washington University School of Medicine

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 19, 2026