[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"paternal-postpartum-depression\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:paternal-postpartum-depression":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,50,64],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100054124","feasibility-and-acceptability-of-a-novel-digital-intervention-to-prevent-paternal-postpartum-depression-100054124",false,"NCT07594743","Feasibility and Acceptability of a Novel Digital Intervention to Prevent Paternal Postpartum Depression","Pilot Randomized Trial of Together in Parenting, a Novel Digital Paternal Postpartum Depression Prevention Intervention","TIP RCT","Inclusion Criteria:\n\n1. English-speaking (for now, TIP is only available in English)\n2. age \\>18 years old,\n3. smartphone ownership or access to home internet,\n4. partner or patient received or receiving prenatal care from a resident or nurse-practitioner\u002Fmidwifery clinic at the Obstetrics and Gynecologic Care Center (OGCC) at Women \\& Infants Hospital of Rhode Island (WIHRI) or receiving an ultrasound at the WIHRI's Prenatal Diagnosis Center ,\n5. planned delivery or status post delivery at WIHRI.\n\nExclusion Criteria:\n\n1. Any self-reported active diagnosis or history of mental health conditions including depression, anxiety, or other psychiatric condition, as per patient report;\n2. Endorsing active suicidality on intake survey or screening positive on the MDS (≥13)16 or GAD-7 (≥8) at time of enrollment;\n3. prisoners;\n4. infant with genetic abnormality, significant anatomic malformation, or NICU admission at time of enrollment;\n5. inability to consent. If new results on the MDS or GAD-7 indicate a positive screening or the father's infant(s) is diagnosed with a genetic abnormality, significant anatomic malformation, or NICU admission after the enrollment and randomization period, the father will still be eligible to continue participation in the study. This information will be tracked in the REDCap database.",true,"ALL","18 Years",{"count":21,"type":22},90,"ESTIMATED","INTERVENTIONAL",[25],"NA","Postpartum depression (PPD) occurs almost as often among men as it does among women. However, while there have been multiple programs designed to prevent maternal PPD, few, if any, interventions exist that have been created specifically to prevent paternal PPD. After engaging in evidence-based qualitative research with soon-to-be or new fathers, a novel interpersonal-therapy based digital program was created to prevent paternal PPD called Together in Parenting (TIP), which comprises multiple podcasts and digital educational handouts. The proposed pilot study will examine the feasibility and acceptability of using TIP as a paternal PPD intervention, will determine the optimal timing of administering TIP to future\u002Fnew fathers, and will generate preliminary estimates of effect of the intervention to support a future efficacy study.",[28,29],"Paternal Postpartum Depression","Postpartum Anxiety",[31,32,33,34,35,36],"paternal postpartum depression","paternal postpartum anxiety","maternal postpartum depression","postpartum perceived stress","maternal postpartum anxiety","dyadic adjustment","RECRUITING","2026-07-09",{"date":40,"type":41},"2026-07-13","ACTUAL",{"date":43,"type":41},"2026-07-07",{"date":45,"type":22},"2027-12-01",{"name":47,"class":48},"Women and Infants Hospital of Rhode Island","OTHER",1,{"id":51,"slug":4,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":23,"phases":53,"briefSummary":26,"conditions":54,"keywords":55,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":63,"locationsCount":4},"100638818",{"count":21,"type":22},[25],[28,29],[31,32,33,34,35,36],"NOT_YET_RECRUITING","2026-05-12",{"date":59,"type":41},"2026-05-19",{"date":61,"type":22},"2026-06-01",{"date":45,"type":22},{"name":47,"class":48},{"id":65,"slug":66,"hasResults":11,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":4,"eligibilityCriteria":70,"healthyVolunteers":11,"sex":71,"minAge":72,"maxAge":73,"enrollmentInfo":74,"targetDuration":4,"studyType":23,"phases":76,"briefSummary":77,"conditions":78,"keywords":82,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":49},"100604612","technology-supported-mindfulness-for-prenatal-depression-and-mental-health-related-quality-of-life-in-a-resource-limited-environment-100604612","NCT07151781","Technology Supported Mindfulness for Prenatal Depression and Mental Health-related Quality of Life in a Resource-Limited Environment","Technology Supported Mindfulness for Prenatal Depression and Mental Health-related Quality of Life: Research Protocol for Randomized Controlled Trial in a Resource-Limited Environment","Inclusion Criteria:\n\n* Pregnant women who lived in Jimma City for at least six months\n* Women with a gestational age between 12 and 28 weeks,\n* Women who scored EPDS ≥ 13,\n* Willing to participate for eight consecutive weeks,\n* Able to attend the health center three times per week and gave consent to be followed up by study supervisors and data collectors\n\nExclusion Criteria:\n\n* Having been diagnosed with mental health disorders or eating disorders,\n* Active substance use,\n* EPDS item 10 score ≥1 or total EPDS score \\>19,\n* Currently receiving pharmacological or psychotherapeutic treatment,\n* Regularly practice meditation,\n* Severely ill,\n* Has active pregnancy-related complications that could interfere with attending the mindfulness exercise, or neurological conditions such as epilepsy or seizures","FEMALE","15 Years","49 Years",{"count":75,"type":22},120,[25],"The goal of this clinical trial is to learn if a video-guided mindfulness intervention can improve prenatal depression symptoms, improve mental health-related quality of life, reduce the risk of maternal postpartum depression and paternal postpartum depression, and improve neonatal birth outcomes in a resource-constrained setting. This clinical trial will be conducted in pregnant women. The main questions it aims to answer are:\n\n* Can video-guided mindfulness intervention be effective for prenatal depression treatment as compared to routine care?\n* Is there a dose-response relationship between the length of a video-guided mindfulness intervention and a reduction in prenatal depression symptoms?\n* Does a video-guided mindfulness intervention improve mental health-related quality of life more effectively than routine care?\n* What is the impact of intervention duration on the effectiveness of a video-guided mindfulness intervention for improving mental health-related quality of life?\n* Can a video-guided mindfulness intervention during pregnancy lead to improved neonatal birth outcomes compared to standard care?\n* Can a video-guided mindfulness intervention during pregnancy reduce the risk of developing prenatal depression compared to routine care?\n* Can the treatment of maternal prenatal depression through a video-guided mindfulness intervention reduce the risk of paternal postpartum depression? Researchers will compare the intervention group with a group of pregnant women who screen positive for prenatal depression but continue to receive only routine antenatal care, in order to evaluate differences in prenatal depression symptoms, improvements in mental health-related quality of life, reductions in the risk of maternal and paternal postpartum depression, and improvements in neonatal birth outcomes.\n\nParticipants (the intervention group) will receive a video-guided mindfulness intervention that they will listen to for eight weeks at their nearest health center three times a week.",[79,80,81,28],"Prenatal Depression","Mental Health Related Quality of Life","Maternal Postpartum Depression",[83,84,85,86,87,88],"mHealth","mindfulness","prenatal depression","randomized controlled trial","health technology","RCT","2025-08-25",{"date":91,"type":41},"2025-09-03",{"date":93,"type":22},"2025-11-01",{"date":95,"type":22},"2025-12-31",{"name":97,"class":48},"Bekelu Teka Worku"]