[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100599408":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":12,"centralContacts":24,"locations":30,"responsibleParty":45,"collaborators":47,"id":50,"slug":51,"hasResults":52,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":12,"eligibilityCriteria":56,"healthyVolunteers":52,"sex":57,"minAge":58,"maxAge":12,"enrollmentInfo":59,"targetDuration":12,"studyType":62,"phases":63,"briefSummary":65,"conditions":66,"keywords":72,"overallStatus":32,"whyStopped":12,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},{"fullName":5,"class":6},"Sakarya University","OTHER",[8,13],{"label":9,"type":10,"description":11,"interventionNames":12},"Usual Care","NO_INTERVENTION","Participants in the control arm will receive routine prenatal care as provided by their healthcare providers. No additional psychosocial support or structured intervention will be administered beyond the standard medical and obstetric services.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"\"Psychosocial Support Intervention\"","EXPERIMENTAL","Participants in the intervention arm will receive a structured psychosocial support program designed for women diagnosed with fetal anomaly. The program includes individual counseling sessions, stress management techniques, emotional support, and educational materials addressing coping strategies and mental well-being. The intervention will be delivered by trained healthcare professionals over sessions during the prenatal period.",[18],"Behavioral: Psychosocial Support Intervention",[20],{"type":21,"name":22,"description":16,"armGroupLabels":23,"otherNames":12},"BEHAVIORAL","Psychosocial Support Intervention",[14],[25],{"name":26,"role":27,"phone":28,"phoneExt":12,"email":29},"Semiha Ünkazan, Master of Licance","CONTACT","+905312052045","semihaunkazan@sakarya.edu.tr",[31],{"facility":5,"status":32,"city":33,"state":34,"zip":35,"country":36,"countryCode":12,"cosmosGeoPoint":37,"geoPoint":42,"contacts":43},"RECRUITING","Sakarya","Türkiye\u002FSakarya","54050","Turkey (Türkiye)",{"type":38,"coordinates":39},"Point",[40,41],32.07583,39.50333,{"lat":41,"lon":40},[44],{"name":5,"role":27,"phone":12,"phoneExt":12,"email":12},{"type":46,"investigatorFullName":12,"investigatorTitle":12,"investigatorAffiliation":12,"oldNameTitle":12,"oldOrganization":12},"SPONSOR",[48],{"name":49,"class":6},"The Scientific and Technological Research Council of Turkey","100599408","effectiveness-of-a-psychosocial-support-intervention-for-women-diagnosed-with-fetal-anomaly-100599408",false,"NCT07084103","Effectiveness of a Psychosocial Support Intervention for Women Diagnosed With Fetal Anomaly","Effectiveness of a Psychosocial Support Intervention for Women Diagnosed With Fetal Anomaly: Randomised Controlled Trial","Inclusion Criteria:\n\n* In her current pregnancy, the results of the dual or triple screening test (a screening test result of 1:50 or 1:100 is considered a high risk for Down syndrome (Şirin, 2020) and\u002For ultrasound findings (physical\u002Fanatomical and congenital anomalies) indicate a high risk of foetal abnormalities,\n* Decision to continue the pregnancy,\n* Being over 18 years of age,\n* Having received hospital services at least once after the initial diagnosis (this criterion was added to enable the pregnant woman to evaluate the services she received from the hospital after the diagnosis and to express her expectations beyond the services provided)\n* No mental or psychological disorders that would make it difficult to express oneself,\n* Voluntary participation in the study.\n\nExclusion Criteria:\n\n• Pregnant women who do not meet the inclusion criteria will be excluded from the sample.","FEMALE","18 Years",{"count":60,"type":61},64,"ESTIMATED","INTERVENTIONAL",[64],"NA","This study aims to evaluate the effectiveness of a psychosocial support intervention for women diagnosed with fetal anomaly. A randomized controlled trial design will be used, and women diagnosed with fetal anomaly will be included as participants. The intervention group will receive a structured psychosocial support program, while the control group will receive routine care.",[67,68,69,70,71],"Fetal Diseases","Congenital Abnormalities","Pregnant Women","Psychosocial Support Systems","Mental Health",[73,74,75,76,77,78,79,80,81],"Fetal anomaly","Congenital abnormalities","Psychosocial support","Psychological intervention","Pregnant women","Prenatal diagnosis","Mental health","Coping strategies","Emotional well-being","2025-07-16",{"date":84,"type":85},"2025-07-24","ACTUAL",{"date":87,"type":85},"2025-04-01",{"date":89,"type":61},"2026-03-31",{"name":5,"class":6},1]