[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100622138":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":11,"centralContacts":11,"locations":19,"responsibleParty":37,"collaborators":11,"id":39,"slug":11,"hasResults":40,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":11,"eligibilityCriteria":44,"healthyVolunteers":40,"sex":45,"minAge":46,"maxAge":47,"enrollmentInfo":48,"targetDuration":11,"studyType":51,"phases":52,"briefSummary":54,"conditions":55,"keywords":57,"overallStatus":22,"whyStopped":11,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},{"fullName":5,"class":6},"King's College Hospital NHS Trust","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Intervention","EXPERIMENTAL",null,[13],"Behavioral: Brief psychological intervention including attention training",[15],{"type":16,"name":17,"description":17,"armGroupLabels":18,"otherNames":11},"BEHAVIORAL","Brief psychological intervention including attention training",[9],[20],{"facility":21,"status":22,"city":23,"state":11,"zip":11,"country":24,"cosmosGeoPoint":25,"geoPoint":30,"contacts":31},"King's College Hospital","RECRUITING","London","United Kingdom",{"type":26,"coordinates":27},"Point",[28,29],-0.12574,51.50853,{"lat":29,"lon":28},[32],{"name":33,"role":34,"phone":35,"phoneExt":11,"email":36},"Kendra Shaw","CONTACT","+4420 3299 8330","kendra.shaw@nhs.net",{"type":38,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100622138",false,"NCT07379723","Brief Intervention for FCD: A Feasibility Study","Feasibility Pilot Study of a Brief Intervention in Functional Cognitive Disorder","Inclusion Criteria:\n\n* Adults aged 65 or below\n* Meet criteria for diagnosis of FCD (criteria include normal MRI results with no neurological diagnosis, and symptoms that are not explained by any other medical condition, performance at routine pre-baseline neuropsychological assessment within the service)\n* Not taking part in any other intervention study or trial\n\nExclusion Criteria:\n\n* Aged above 65 years\n* Lack capacity to consent\n* MRI results not in normal range\n* Neurological diagnosis\n* Indication of severe low mood or depression (from clinical interview, routine measures)\n* Taking part in any other intervention study or trial","ALL","18 Years","65 Years",{"count":49,"type":50},30,"ESTIMATED","INTERVENTIONAL",[53],"NA","The goal of this study is to learn if a single session intervention for people with Functional Cognitive Disorder (FCD) is feasible and acceptable. The main questions it aims to answer are:\n\nWhat is the impact of a single session intervention on FCD symptoms, functional impairment, and quality of life in people with FCD?\n\nWhat is the feasibility and acceptability of piloting a single session intervention for people with FCD.\n\nParticipants will:\n\n* Complete questionnaires about cognitive concerns, anxiety, depression, functional impairment and quality of life\n* Visit the clinic for a single session intervention including practicing the Attention Training Technique (ATT)\n* Complete 2 telephone calls with a researcher to discuss their use of the intervention and to complete the same questionnaires from their clinic visit, and a questionnaire about their experience of the study and intervention.",[56],"Functional Cognitive Disorder",[56,58,59,60,61],"Brief Interventions","Feasibility","Pilot","Attention Training","2026-01-23",{"date":64,"type":65},"2026-01-30","ACTUAL",{"date":67,"type":65},"2025-11-11",{"date":69,"type":50},"2026-05-01",{"name":5,"class":6},1]