[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100624264":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":28,"locations":10,"responsibleParty":34,"collaborators":36,"id":42,"slug":43,"hasResults":44,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":44,"sex":50,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":10,"studyType":56,"phases":10,"briefSummary":57,"conditions":58,"keywords":63,"overallStatus":73,"whyStopped":10,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":10},{"fullName":5,"class":6},"Swissmed Hospital","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Women with PPAWIS (Routine Care)",null,"Participants are women diagnosed with postpartum abdominal wall insufficiency syndrome (PPAWIS) receiving routine clinical care as determined by the treating clinicians and patient preferences. Management include surgical approaches according to usual practice. No intervention is assigned by the research protocol. Patient-reported outcome measures are collected at baseline and during follow-up.",[13],"Other: Routine Clinical Care",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":10},"Routine Clinical Care","No intervention is assigned by the research protocol. Clinical management is determined by clinicians and patients according to usual practice; the study collects patient-reported outcome measures longitudinally.",[9],[20,24],{"name":21,"affiliation":22,"role":23},"Maciej Śmietański, Prof.","Śmietański Hernia Center, LUX MED Hospital in Gdańsk","PRINCIPAL_INVESTIGATOR",{"name":25,"affiliation":26,"role":27},"Sylwia Jędrzejewska, MD, PhD","Polish Sexological Society","STUDY_CHAIR",[29],{"name":30,"role":31,"phone":32,"phoneExt":10,"email":33},"Magdalena Halska","CONTACT","607 870 690","worldofsurge@gmail.com",{"type":35,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[37,39],{"name":38,"class":6},"Medical University of Gdansk",{"name":40,"class":41},"Śmietański Hernia Center","UNKNOWN","100624264","patient-reported-outcomes-in-women-with-postpartum-abdominal-wall-insufficiency-ppawis-100624264",false,"NCT07407374","Patient-Reported Outcomes in Women With Postpartum Abdominal Wall Insufficiency (PPAWIS)","A Prospective Observational Cohort Study of Quality of Life, Body Image, and Sexual Function in Women With Postpartum Abdominal Wall Insufficiency Syndrome (PPAWIS) Using Patient-Reported Outcome Measures","EMPOWER","Inclusion Criteria:\n\n* Female, age 18-65 years\n* Postpartum status: at least 6 months after last delivery\n* Clinical diagnosis of postpartum abdominal wall insufficiency syndrome (PPAWIS), defined by abdominal wall dysfunction symptoms and\u002For significant quality-of-life impact, with supportive findings on physical examination and\u002For imaging (e.g., diastasis recti and\u002For related abdominal wall insufficiency features)\n* Receiving routine clinical care for PPAWIS at the study site (surgical)\n* Able and willing to provide informed consent and complete patient-reported outcome questionnaires at baseline and follow-up\n\nExclusion Criteria:\n\n* Current pregnancy\n* Planned pregnancy during the follow-up period (up to 12 months), if expected to interfere with outcome assessment\n* Inability to complete questionnaires due to cognitive impairment or insufficient language proficiency in the validated questionnaire language version\n* Severe uncontrolled psychiatric condition that, in the investigator's opinion, would prevent informed consent or reliable questionnaire completion\n* Participation in another interventional study that could materially affect patient-reported outcomes related to abdominal wall function during the follow-up period","FEMALE","18 Years","65 Years",{"count":54,"type":55},30,"ESTIMATED","OBSERVATIONAL","Postpartum abdominal wall insufficiency syndrome (PPAWIS) is a multidimensional condition that may affect physical function, quality of life, body image, and sexual health in women after childbirth. Anatomical findings alone do not fully explain symptom burden or patient experience.\n\nThis prospective observational cohort study will collect validated patient-reported outcome measures (PROMs) from women with PPAWIS receiving routine care. PROMs will be assessed at baseline and during follow-up to describe symptom burden and changes over time. The study aims to improve understanding of the patient-centered impact of PPAWIS and to support development of standardized assessment pathways in clinical practice.",[59,60,61,62],"Diastasis Recti and Weakness of the Linea Alba","Abdominal Wall Defect","Postpartum Complication","Abdominal Wall Anomaly",[64,65,66,67,68,69,70,71,72],"PROMs","postpartum abdominal wall insufficiency","PPAWIS","patient-reported outcomes","sexual function","women's health","core stability","quality of life","abdominal wall reconstruction","NOT_YET_RECRUITING","2026-02-05",{"date":76,"type":77},"2026-02-12","ACTUAL",{"date":79,"type":55},"2026-02-20",{"date":81,"type":55},"2027-01-01",{"name":5,"class":6}]