[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100622138":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":11,"centralContacts":11,"locations":19,"responsibleParty":38,"collaborators":11,"id":40,"slug":41,"hasResults":42,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":11,"eligibilityCriteria":46,"healthyVolunteers":42,"sex":47,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":11,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":22,"whyStopped":11,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":73},{"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,"countryCode":25,"cosmosGeoPoint":26,"geoPoint":31,"contacts":32},"King's College Hospital","RECRUITING","London","United Kingdom","UK",{"type":27,"coordinates":28},"Point",[29,30],-0.12574,51.50853,{"lat":30,"lon":29},[33],{"name":34,"role":35,"phone":36,"phoneExt":11,"email":37},"Kendra Shaw","CONTACT","+4420 3299 8330","kendra.shaw@nhs.net",{"type":39,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100622138","brief-intervention-for-fcd-a-feasibility-study-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":51,"type":52},30,"ESTIMATED","INTERVENTIONAL",[55],"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.",[58],"Functional Cognitive Disorder",[58,60,61,62,63],"Brief Interventions","Feasibility","Pilot","Attention Training","2026-01-23",{"date":66,"type":67},"2026-01-30","ACTUAL",{"date":69,"type":67},"2025-11-11",{"date":71,"type":52},"2026-05-01",{"name":5,"class":6},1]