[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100618721":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":12,"locations":17,"responsibleParty":36,"collaborators":7,"id":38,"slug":39,"hasResults":40,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":7,"eligibilityCriteria":44,"healthyVolunteers":40,"sex":45,"minAge":46,"maxAge":7,"enrollmentInfo":47,"targetDuration":7,"studyType":50,"phases":7,"briefSummary":51,"conditions":52,"keywords":7,"overallStatus":20,"whyStopped":7,"lastUpdateSubmitDate":54,"lastUpdatePostDateStruct":55,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":63},{"fullName":5,"class":6},"M.D. Anderson Cancer Center","OTHER",null,[9],{"name":10,"affiliation":5,"role":11},"Ann H Klopp, MD, PHD","PRINCIPAL_INVESTIGATOR",[13],{"name":10,"role":14,"phone":15,"phoneExt":7,"email":16},"CONTACT","(713) 563-2444","aklopp@mdanderson.org",[18],{"facility":19,"status":20,"city":21,"state":22,"zip":23,"country":24,"countryCode":25,"cosmosGeoPoint":26,"geoPoint":31,"contacts":32},"The University of Texas M. D. Anderson Cancer Center","RECRUITING","Houston","Texas","77030","United States","US",{"type":27,"coordinates":28},"Point",[29,30],-95.36327,29.76328,{"lat":30,"lon":29},[33,35],{"name":10,"role":14,"phone":34,"phoneExt":7,"email":16},"713-563-2444",{"name":10,"role":11,"phone":7,"phoneExt":7,"email":7},{"type":37,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100618721","care-bia-pilot-study-to-improve-patient-comfort-and-reduce-psychological-distress-during-ia-removal-100618721",false,"NCT07335302","CARE-BI:a Pilot Study to Improve Patient Comfort and Reduce Psychological Distress During IA Removal","CARE-BI (Comfort and Analgesia for Removal of Brachytherapy Implants): a Pilot Study to Improve Patient Comfort and Reduce Psychological Distress During Intracavitary Applicator Removal","Inclusion Criteria:\n\n* Capable of signing informed consent\n* Age ≥ 18 years old\n* Receipt of multiple intracavitary brachytherapy treatments for gynecologic cancer\n* Capable of completing PRO and patient satisfaction surveys and willing to comply with completion of surveys multiple times throughout and after treatment\n\nExclusion Criteria:\n\n* Patients without ability to sign informed consent\n* Patients unwilling or unable to complete PRO and patient satisfaction surveys at the times required by the study","ALL","18 Years",{"count":48,"type":49},36,"ESTIMATED","OBSERVATIONAL","The goal of this research study is to learn about the rate of posttraumatic stress disorder (PTSD) experienced by women after undergoing gynecologic brachytherapy.",[53],"Psychological Distress","2026-07-15",{"date":56,"type":57},"2026-07-16","ACTUAL",{"date":59,"type":57},"2025-12-18",{"date":61,"type":49},"2028-10-20",{"name":5,"class":6},1]