Condition: Depression · MDD · Major Depressive Disorder · Sponsor: NYU Langone Health
This pilot study evaluates the feasibility, safety, and preliminary efficacy of home-based 60Hz intermittent light therapy in adults with a major depressive episode (MDE). Participants will be randomized in a 2:1 ratio to receive either active or sham 60Hz intermittent light stimulation for 30 minutes daily (Monday through Friday) over three weeks. The light is delivered through a wearable headset. Clinical assessments will be conducted remotely at baseline, mid-point, post-treatment, and follow-up to measure changes in depressive symptoms.
This description comes directly from the study's public registry record.
Shayna Pehel · 929-455-5104 · Shayna.Pehel@nyulangone.org
Giuseppina Pilloni · 929-455-5317 · Giuseppina.Pilloni@nyulangone.org
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| NYU Langone Health | New York, New York, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07111390