Clinical Trial: Informing Implementation of a Circadian-Focused Intervention for Postpartum Depression

U.S., Aug. 15 -- ClinicalTrials.gov registry received information related to the study (NCT07766161) titled 'Informing Implementation of a Circadian-Focused Intervention for Postpartum Depression' on Aug. 05.

Brief Summary: The proposed study is an open-label trial of Re-Timer(R) 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.

Study Start Date: July 29

Study Type: INTERVENTIONAL

Condition: Postpartum Depression (PPD)

Intervention: DEVICE: Light therapy

Participants will use the Re-Timer daily for 5 weeks (approximately 35 days). All participants will be pro...