[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"ptsd-childbirth-related\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:ptsd-childbirth-related":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,48,78,103],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100646910","debriefing-consult-for-psychiatric-symptoms-after-severe-maternal-morbidity-100646910",false,"NCT07684521","Debriefing Consult for Psychiatric Symptoms After Severe Maternal Morbidity","Does a Debriefing Intervention After a Delivery Complicated by Severe Maternal Morbidity Reduce Post-traumatic, Depression, or Anxiety Symptoms? A Randomized Controlled Trial","Inclusion Criteria:\n\n\\- Individuals with a delivery complicated by severe maternal morbidity, defined as intensive care unit (ICU) admission and\u002For blood product transfusion \\>4 units\n\nExclusion Criteria:\n\n* Age \\\u003C18 years\n* Non-English speakers\n* Any records flagged \"break the glass\" or \"research opt out\"","FEMALE","18 Years",{"count":19,"type":20},52,"ESTIMATED","INTERVENTIONAL",[23],"NA","The primary objective of this study is to determine if a maternal fetal medicine (MFM) debriefing consult six to eight weeks postpartum reduces self-reported post-traumatic stress, depression, and anxiety symptoms following a delivery complicated by severe maternal morbidity (SMM). Individuals with a delivery complicated an intensive care unit (ICU) admission and\u002For blood product transfusion \\>4 units will be included in this study. Participants will be randomized to an intervention or control group; all participants will complete patient questionnaires that screen for post-traumatic stress disorder, depression, and anxiety. Those in the control group will receive a virtual MFM debriefing consult at six weeks postpartum and those in the intervention group will have the option for a consult at twelve weeks postpartum, after the completion of the questionnaires.",[26,27,28,29],"PTSD (Childbirth-Related)","Severe Maternal Morbidity","Depression - Major Depressive Disorder","Anxiety",[31,32,33,34],"severe materal morbidity","PTSD","anxiety","depression","NOT_YET_RECRUITING","2026-06-29",{"date":38,"type":39},"2026-07-06","ACTUAL",{"date":41,"type":20},"2026-07-01",{"date":43,"type":20},"2030-07",{"name":45,"class":46},"Cedars-Sinai Medical Center","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":21,"phases":58,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":47},"100606397","the-new-empowerment-after-exposure-to-trauma-next-study-100606397","NCT07175025","The New Empowerment After eXposure to Trauma (NEXT) Study","NEXT","Inclusion Criteria:\n\n* 18 years of age or older\n* able to read and speak English\n* diagnosis of probable PTSD as determined by the PTSD Checklist for DSM-5 (PCL-5)\n* pregnant or postpartum (delivered within 12 weeks) at the time of the eligibility screen Exclusion criteria\n* current severe suicide risk as determined by the Columbia Suicide Severity Rating Scale Screener (C-SSRS)\n* current psychotic or manic symptoms as determined by the DIAMOND screener and the Mood Disorder Questionnaire for Bipolar Disorder\n* cognitive impairment\n* concurrent trauma-focused psychotherapy\n* medical advice limiting participation in exposure therapy\n* current legal actions related to trauma\n* does not meet criteria for PTSD\n* not pregnant or delivered more than 12 weeks after timing of eligibility screening","50 Years",{"count":57,"type":20},106,[23],"The NEXT Study is a randomized controlled pilot examining the feasibility and acceptability of a revised perinatal PTSD protocol. This study will randomize perinatal participants with PTSD to receive NET (n=45); treatment group) and will be compared to perinatal women randomized to usual care (n=45; comparator group). The overall objective of this project is to determine the most feasible and acceptable protocol for a brief virtual perinatal PTSD intervention.",[61,26],"PTSD - Post Traumatic Stress Disorder",[63,64,65,66,67],"Pregnancy","Postpartum Period","Narrative Exposure Therapy","Post-Traumatic Stress Disorder","Brief interventions","RECRUITING","2026-06-16",{"date":71,"type":39},"2026-06-18",{"date":73,"type":39},"2025-09-24",{"date":75,"type":20},"2028-07-31",{"name":77,"class":46},"Indiana University",{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":21,"phases":87,"briefSummary":88,"conditions":89,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":102},"100619277","early-intervention-for-postpartum-ptsd-comparing-written-exposure-and-capnometry-guided-breathing-therapy-100619277","NCT07342530","Early Intervention for Postpartum PTSD: Comparing Written Exposure and Capnometry-Guided Breathing Therapy","Early Intervention for Postpartum PTSD: Comparing Written Exposure and Capnometry Guided Breathing Therapy","Inclusion Criteria:\n\n* Age ≥18\n* Delivered a live infant within 5 days\n* Severe maternal morbidity or infant admitted to NICU\n* PCL-5 ≥28\n* English-speaking\n* Able to consent and participate\n\nExclusion Criteria:\n\n* Active psychosis or mania\n* Current suicidal crisis\n* Current suicidal intent or plan\n* Cognitive impairment preventing participation",{"count":86,"type":20},70,[23],"The purpose of this study is to examine two early interventions, Written Exposure Therapy and Capnometry Guided Breathing, to reduce post-traumatic stress disorder (PTSD) symptoms in women after childbirth as compared to usual care.",[90,91,26,92],"Written Exposure Therapy","Breathing Techniques","Postpartum Care","2026-04-21",{"date":95,"type":39},"2026-04-24",{"date":97,"type":39},"2026-03-09",{"date":99,"type":20},"2027-12",{"name":101,"class":46},"Stanford University",2,{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":4,"eligibilityCriteria":109,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":110,"enrollmentInfo":111,"targetDuration":4,"studyType":21,"phases":113,"briefSummary":114,"conditions":115,"keywords":118,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":47},"100611882","feasibility-and-efficacy-of-gtep-for-birth-trauma-100611882","NCT07246356","Feasibility and Efficacy of GTEP for Birth Trauma","A Study to Explore the Feasibility and Efficacy of Group Traumatic Episode Protocol (GTEP) for Reducing Trauma Symptoms Following a Traumatic Birthing Experience","Inclusion Criteria:\n\n* Aged between 18-65 years.\n* Currently under the Black Country Perinatal Mental Health Service\n* Experiencing self-reported trauma symptoms related to a birthing experience within the last 18 months (this includes the birth itself, the postnatal hospital stay, and\u002For any neonatal admissions).\n* Access to technology (e.g., laptop, internet connection) to be able to access the online group.\n* Access to a confidential space within their home, and childcare for their baby\u002Fany other existing children.\n* Proficient levels of English Language to engage with the group.\n* Ability to engage in group therapy based on clinical presentation.\n* Capacity to consent to engage in the GTEP group and research study.\n\nExclusion Criteria:\n\n* Women\u002Fbirthing people whose baby is no longer under their care.\n* Severe and enduring mental health presentations (i.e., diagnosis of bipolar, psychosis and\u002For schizophrenia.\n* Significant sensory impairment (e.g., needing a British Sign Language interpreter).","65 Years",{"count":112,"type":20},10,[23],"This clinical study aims to evaluate the feasibility and initial efficacy of Group Traumatic Episode Protocol (GTEP) for reducing trauma symptoms (measured by the PCL-5 and City BiTS) for individuals following a traumatic birthing experience. A secondary aim is to evaluate the efficacy of GTEP in improving parental wellbeing (measured through the CORE-10) and parent-infant bonding (measured through the PBQ) following a traumatic birthing experience.\n\nParticipants (those who have experienced a traumatic birthing experience) will complete the GTEP intervention, delivered online. They will be asked to complete outcome measures and give feedback on their experience of the group.",[26,116,117],"Psychological Wellbeing","Bonding",[119,120,121,122,123,124],"GTEP","Group EMDR","Birth trauma","Psychological wellbeing","Perinatal","Parent infant bonding","2026-02-18",{"date":127,"type":39},"2026-02-19",{"date":129,"type":39},"2025-06-19",{"date":131,"type":20},"2026-06-30",{"name":133,"class":46},"University of Birmingham"]