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Informing Implementation of a Circadian-Focused Intervention for Postpartum Depression
Sponsor: University of Michigan
Summary
The proposed study is an open-label trial of Re-Timer® wearable morning bright light therapy for postpartum depression. The study is focused on evaluating the feasibility, acceptability, and implementation context of morning Bright Light Treatment (mBLT) for postpartum depression.
Key Details
Gender
FEMALE
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
30
Start Date
2026-07-29
Completion Date
2027-05
Last Updated
2026-08-14
Healthy Volunteers
No
Conditions
Interventions
Light therapy
Participants will use the Re-Timer daily for 5 weeks (approximately 35 days). All participants will be provided with a "light therapy window" during which they will wear the device for 60 mins.
Locations (1)
University of Michigan
Ann Arbor, Michigan, United States