[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100651838":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":24,"locations":30,"responsibleParty":47,"collaborators":50,"id":53,"slug":54,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":57,"acronym":19,"eligibilityCriteria":58,"healthyVolunteers":55,"sex":59,"minAge":60,"maxAge":19,"enrollmentInfo":61,"targetDuration":19,"studyType":64,"phases":65,"briefSummary":67,"conditions":68,"keywords":70,"overallStatus":32,"whyStopped":19,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":81},{"fullName":5,"class":6},"University of Michigan","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Light therapy","EXPERIMENTAL","Participants in the arm will be approximately 30 women who are within 6 months postpartum and have an Edinburgh Postnatal Depression Scale (EPDS) score \\> 10.",[13],"Device: Light therapy",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":19},"DEVICE","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.",[9],null,[21],{"name":22,"affiliation":5,"role":23},"Leslie Swanson, PhD","PRINCIPAL_INVESTIGATOR",[25],{"name":26,"role":27,"phone":28,"phoneExt":19,"email":29},"Kelley DuBuc","CONTACT","734-764-1904","dubuck@med.umich.edu",[31],{"facility":5,"status":32,"city":33,"state":34,"zip":35,"country":36,"countryCode":37,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"RECRUITING","Ann Arbor","Michigan","48109","United States","US",{"type":39,"coordinates":40},"Point",[41,42],-83.74088,42.27756,{"lat":42,"lon":41},[45,46],{"name":26,"role":27,"phone":28,"phoneExt":19,"email":29},{"name":22,"role":23,"phone":19,"phoneExt":19,"email":19},{"type":23,"investigatorFullName":48,"investigatorTitle":49,"investigatorAffiliation":5,"oldNameTitle":19,"oldOrganization":19},"Leslie Swanson","Clinical Professor of Psychiatry",[51],{"name":52,"class":6},"American Academy of Sleep Medicine","100651838","informing-implementation-of-a-circadian-focused-intervention-for-postpartum-depression-100651838",false,"NCT07766161","Informing Implementation of a Circadian-Focused Intervention for Postpartum Depression","Inclusion Criteria:\n\n1. ≤ 6 months postpartum\n2. EPDS score \\>10\n\nExclusion Criteria:\n\n1. Current or past-year substance use disorder\n2. Lifetime history of bipolar disorder or psychotic disorder\n3. Active suicidal intent\n4. Retinal pathology or history of eye surgery\n5. Current use of photosensitizing medications\n6. Untreated sleep-disordered breathing, untreated restless legs syndrome, or narcolepsy\n7. Psychotherapy or psychotropic medications started\u002Fdose changed in past month (psychotherapy started and\u002For current medication at stable dose ≥ 4 weeks are permitted)\n8. Medical conditions contraindicated for mBLT (e.g., epilepsy\u002Fseizures)","FEMALE","18 Years",{"count":62,"type":63},30,"ESTIMATED","INTERVENTIONAL",[66],"NA","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.",[69],"Postpartum Depression (PPD)",[71,9],"Circadian rhythm","2026-08-10",{"date":74,"type":75},"2026-08-14","ACTUAL",{"date":77,"type":75},"2026-07-29",{"date":79,"type":63},"2027-05",{"name":5,"class":6},1]