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RECRUITING
NCT07111390
NA

Feasibility of Home-Based Intermittent 60Hz Light Therapy for Major Depressive Disorder (MDD)

Sponsor: NYU Langone Health

View on ClinicalTrials.gov

Summary

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.

Official title: A Feasibility Pilot Study of Home-Based Intermittent 60Hz Light Therapy for the Treatment of Depression

Key Details

Gender

All

Age Range

24 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2025-08-18

Completion Date

2026-03-01

Last Updated

2025-08-26

Healthy Volunteers

No

Interventions

DEVICE

60Hz Intermittent Light Therapy

Intermittent 60 Hz flickering white light delivered via a wearable headset.

DEVICE

Sham Light Therapy

Constant white light delivered via a wearable headset.

Locations (1)

NYU Langone Health

New York, New York, United States