[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100608667":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":18,"centralContacts":23,"locations":34,"responsibleParty":64,"collaborators":10,"id":66,"slug":10,"hasResults":67,"nctId":68,"briefTitle":69,"officialTitle":69,"acronym":70,"eligibilityCriteria":71,"healthyVolunteers":67,"sex":72,"minAge":73,"maxAge":10,"enrollmentInfo":74,"targetDuration":77,"studyType":78,"phases":10,"briefSummary":79,"conditions":80,"keywords":82,"overallStatus":37,"whyStopped":10,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":95},{"fullName":5,"class":6},"Centre Paul Strauss","OTHER",[8],{"label":9,"type":10,"description":10,"interventionNames":11},"Patient with cervical cancer with an indication for uterovaginal brachytherapy",null,[12],"Other: Prospective questionnaires",[14],{"type":6,"name":15,"description":16,"armGroupLabels":17,"otherNames":10},"Prospective questionnaires","Post-traumatic stress disorder Checklist version DSM-5 (PCL-5) and quality of life questionnaires",[9],[19],{"name":20,"affiliation":21,"role":22},"George NOEL, MD, PhD","ICANS, CPS","PRINCIPAL_INVESTIGATOR",[24,30],{"name":25,"role":26,"phone":27,"phoneExt":28,"email":29},"Valérie SARTORI","CONTACT","368767223","33","promotion-rc@icans.eu",{"name":31,"role":26,"phone":32,"phoneExt":28,"email":33},"Claire VIT","388258529","c.vit@icans.eu",[35,52],{"facility":36,"status":37,"city":38,"state":10,"zip":39,"country":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"Groupement Hospitalier Sud - Hopital Lyon Sud","RECRUITING","Pierre-Bénite","69495","France",{"type":42,"coordinates":43},"Point",[44,45],4.82424,45.70359,{"lat":45,"lon":44},[48],{"name":49,"role":26,"phone":50,"phoneExt":10,"email":51},"Ionela CARAIVAN, MD","0478864251","promotion-rc@institut-strauss.fr",{"facility":53,"status":37,"city":54,"state":10,"zip":55,"country":40,"cosmosGeoPoint":56,"geoPoint":60,"contacts":61},"ICANS","Strasbourg","67033",{"type":42,"coordinates":57},[58,59],7.74553,48.58392,{"lat":59,"lon":58},[62],{"name":20,"role":26,"phone":63,"phoneExt":28,"email":29},"368766767",{"type":65,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100608667",false,"NCT07204535","Post-TRaUmatic STress Disorder Induced by Gynecological Brachytherapy","TRUST-GB","Inclusion Criteria:\n\n* Confirmed diagnosis of cervical cancer with an indication for High-dose rate (HDR) or pulse-dose rate (PDR) uterovaginal brachytherapy;\n* Squamous cell carcinoma or other histological types;\n* WHO ≤ 2;\n* Ability to complete validated questionnaires in French;\n* Informed consent to participate in the study;\n* Patients over 18 years old\n\nExclusion Criteria:\n\n* Inability to understand or respond to questionnaires due to a cognitive disorder, intellectual disability, language barrier, or psychiatric disorder that impairs judgment;\n* Patient under juridic protection;\n* Pregnant or breastfeeding woman","FEMALE","18 Years",{"count":75,"type":76},80,"ESTIMATED","60 Months","OBSERVATIONAL","This is a multicenter, prospective study aimed at providing information on the psychological effects (including post-traumatic stress symptoms) of utero-vaginal brachytherapy in patients with cervical cancer using self-administered questionnaires. The study also aims to assess the persistence of these symptoms over time, up to 5 years after brachytherapy. The results could help identify patients at risk of post-traumatic stress in this context and develop appropriate psychological interventions to improve their psychological well-being during and after treatment.",[81],"Uterine Cervical Neoplasms",[83,84,85],"Brachytherapy","Post-TRaUmatic STress Disorder","Cervical cancer","2026-06-03",{"date":88,"type":89},"2026-06-04","ACTUAL",{"date":91,"type":89},"2025-11-17",{"date":93,"type":76},"2031-11-17",{"name":5,"class":6},2]