Brief Intervention for FCD: A Feasibility Study

Recruiting now · Not applicable

Conditions studied: Functional Cognitive Disorder

In brief

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: What is the impact of a single session intervention on FCD symptoms, functional impairment, and quality of life in people with FCD? What is the feasibility and acceptability of piloting a single session intervention for people with FCD. Participants will: * Complete questionnaires about cognitive concerns, anxiety, depression, functional impairment and quality of life * Visit the clinic for a single session intervention including practicing the Attention Training Technique (ATT) * 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.

Key facts

Study ID

NCT07379723

Run by

King's College Hospital NHS Trust

People needed

30

Starts

2025-11-11

Expected to finish

2026-05-01

Last updated by the study team

2026-01-30

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adults aged 65 or below
• 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)
• Not taking part in any other intervention study or trial

You may not qualify if…

• Aged above 65 years
• Lack capacity to consent
• MRI results not in normal range
• Neurological diagnosis
• Indication of severe low mood or depression (from clinical interview, routine measures)
• Taking part in any other intervention study or trial

Where it is running

• King's College Hospital — London, United Kingdom (enrolling)

Full record on ClinicalTrials.gov

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