Actively Recruiting
Brief Intervention for FCD: A Feasibility Study
Led by King's College Hospital NHS Trust · Updated on 2026-01-30
30
Participants Needed
1
Research Sites
24 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Brief Intervention for FCD: A Feasibility Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 65 or below
- Meet criteria for diagnosis of Functional Cognitive Disorder including normal MRI results with no neurological diagnosis
- Symptoms 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 will not qualify if you...
- Aged above 65 years
- Lack capacity to consent
- MRI results not in normal range
- Neurological diagnosis
- Indication of severe low mood or depression
- Taking part in any other intervention study or trial
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
King's College Hospital
London, United Kingdom
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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