[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100551126":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":33,"locations":39,"responsibleParty":69,"collaborators":12,"id":71,"slug":72,"hasResults":73,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":77,"eligibilityCriteria":78,"healthyVolunteers":73,"sex":79,"minAge":80,"maxAge":12,"enrollmentInfo":81,"targetDuration":12,"studyType":84,"phases":85,"briefSummary":87,"conditions":88,"keywords":12,"overallStatus":42,"whyStopped":12,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":101},{"fullName":5,"class":6},"Vrije Universiteit Brussel","OTHER",[8,13],{"label":9,"type":10,"description":11,"interventionNames":12},"Baseline group","NO_INTERVENTION","Receives care as usual after severe perinatal diagnosis",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Perinatal palliative care group","EXPERIMENTAL","Receives a new perinatal palliative care intervention after severe perinatal diagnosis",[18],"Behavioral: Perinatal palliative care",[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":12},"BEHAVIORAL","Perinatal palliative care","Intervention group will receive specialized perinatal palliative care support from moment of severe perinatal diagnosis. This intervention is aimed at 5 major care components, namely 1. Support offered by a fixed perinatal palliative care team, 2. that team has received specialized perinatal palliative care training, 3. care is structured within a new perinatal palliative care approach or pathway, including fixed means of communication with team members, 4. psychological support is structurally being offered to parents and healthcare providers, and 5. debriefings after every perinatal death are being organized in the involved team.",[14],[26,30],{"name":27,"affiliation":28,"role":29},"Filip Cools","Brussels University Hospital","PRINCIPAL_INVESTIGATOR",{"name":31,"affiliation":32,"role":29},"Kristien Roelens","University Hospital, Ghent",[34],{"name":35,"role":36,"phone":37,"phoneExt":12,"email":38},"Laure Dombrecht","CONTACT","+32476046563","laure.dombrecht@vub.be",[40,56],{"facility":41,"status":42,"city":43,"state":12,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"UZ Brussels","RECRUITING","Brussels","1090","Belgium","BE",{"type":48,"coordinates":49},"Point",[50,51],4.34878,50.85045,{"lat":51,"lon":50},[54],{"name":35,"role":36,"phone":55,"phoneExt":12,"email":38},"0476046563",{"facility":57,"status":58,"city":59,"state":12,"zip":60,"country":45,"countryCode":46,"cosmosGeoPoint":61,"geoPoint":65,"contacts":66},"UZ Gent","NOT_YET_RECRUITING","Ghent","9000",{"type":48,"coordinates":62},[63,64],3.71667,51.05,{"lat":64,"lon":63},[67],{"name":35,"role":36,"phone":55,"phoneExt":12,"email":68},"laure.dombrecht@ugent.be",{"type":29,"investigatorFullName":35,"investigatorTitle":70,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"Postdoctoral researcher","100551126","pilot-testing-a-perinatal-palliative-care-intervention-program-100551126",false,"NCT06456034","Pilot-testing a Perinatal Palliative Care Intervention Program","Testing a Perinatal Palliative Care Intervention Program Within Standard Perinatal Healthcare: Pilot Testing Protocol","PPC-pilot","Inclusion Criteria:\n\n* Parents:\n\n  * who receive a severe foetal diagnosis for their unborn child and decide to continue the pregnancy after 20 weeks of gestation , or\n  * who receive a severe foetal diagnosis for their unborn child after 20 weeks gestation and decide to terminate the pregnancy (with or without feticide) resulting in the stillbirth of their child\n* Parents who receive a severe neonatal diagnosis for their live-born infant in the first week after birth\n\nAdditional inclusion criteria for parents:\n\n* Parents are either Dutch speaking, or are willing to participate with support from a (phone or real life) interpreter, in collaboration with the \"Agentschap Integratie \\& Inburgering\"\n* Parents are older than 18\n* Parents are not suffering from an officially diagnosed psychiatric disorder prior to receiving the severe diagnosis of their child\n* Parents are deemed (emotionally) approachable for the current study by the treating physician\n\nFor each family included in the pilot study, the physicians and nurses\u002Fmidwives who will be\u002Fare most closely involved in the care of the infant and the parents will also be asked to participate. If healthcare providers refuse to provide informed consent to participate in the study, their data will be deemed as missing for that case (parental outcomes are considered as the primary outcome measures).","ALL","18 Years",{"count":82,"type":83},20,"ESTIMATED","INTERVENTIONAL",[86],"NA","The objective of this pilot trial is to implement a new perinatal palliative care intervention program tailored to the Flemish context, which aims to provide care to parents who receive a severe foetal\u002Fneonatal diagnosis for their (unborn) child and to their healthcare providers. Additionally, we aim to evaluate the feasibility and preliminary effectiveness by comparing measured variables to the baseline measurement done in the same hospital wards beforehand.",[89,90,91],"Perinatal Palliative Care","Life-limiting Fetal Diagnosis","Life-limiting Neonatal Diagnosis","2025-09-16",{"date":94,"type":95},"2025-09-22","ACTUAL",{"date":97,"type":95},"2025-05-18",{"date":99,"type":83},"2025-12",{"name":5,"class":6},2]