[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"childbirth-related-posttraumatic-stress-disorder\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:childbirth-related-posttraumatic-stress-disorder":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":5},"100631019","cognitive-processing-therapy-for-childbirth-related-post-traumatic-stress-disorder-100631019",false,"NCT07495228","Cognitive Processing Therapy for Childbirth-Related Post-Traumatic Stress Disorder","CB-PTSDCPT","Inclusion Criteria:\n\n* women\u002Fbirthing people aged 18 years and older who are fluent in English (able to speak\u002Funderstand and read English), and who are at least one month postpartum\n* either indicate clinical levels of PTSD related to a traumatic birth (i.e., 31 or higher on the PCL-5) or endorse significant distress or impairment as a result of their traumatic childbirth experience\n* not receiving concurrent psychological treatment\n* not taking psychoactive medication or if taking medications, are stable in dose and type for at least 8 weeks prior to the study (as per Canadian psychiatric guidelines; McQueen et al., 2016) and remain stable throughout the study\n\nExclusion Criteria:\n\n* severe depression\u002Fsuicidality requiring acute intervention\n* medication changes in dose or type","FEMALE","18 Years",{"count":19,"type":20},29,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to determine whether participation in an individual 8-session cognitive processing therapy (CPT) is feasible, acceptable, and leads to clinically meaningful trauma symptom reduction in individuals experiencing childbirth-related trauma.\n\nThe main questions it aims to answer are:\n\n1. Is it feasible for women and birthing people to attend and complete an 8-session course of CPT delivered virtually within a specialized women's mental health clinic?\n2. Do participants find this modified 8-session CPT protocol acceptable and helpful?\n3. Does the treatment lead to clinically meaningful reductions in childbirth-related posttraumatic stress and related symptoms?\n\nParticipants will be asked to:\n\n1. Attend 8 weekly sessions of individual CPT for childbirth-related trauma\n2. Complete a self-report measure of trauma symptoms weekly (i.e., the PCL-5)\n3. Complete additional symptom questionnaires at baseline, post-treatment, and at one-month follow-up.\n4. Complete a brief qualitative interview one week after treatment to share feedback on their experience",[26,27],"Childbirth-Related Posttraumatic Stress Disorder","Childbirth-related Trauma",[29,30,31,26,32,33,34],"Postpartum","Posttraumatic Stress Disorder","Childbirth","Trauma","Cognitive Processing Therapy","mothers","NOT_YET_RECRUITING","2026-03-22",{"date":38,"type":39},"2026-03-27","ACTUAL",{"date":41,"type":20},"2026-04-01",{"date":43,"type":20},"2028-04-01",{"name":45,"class":46},"St. Joseph's Healthcare Hamilton","OTHER"]