At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- Brief psychological intervention including attention training (behavioural)
- How long the study runs
- Study runs about 6 months (dates as stated)
- About the drug or intervention
- Brief psychological intervention including attention training — behavioural: Brief psychological intervention including attention training
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 18 Years to 65 Years
- Who
- All
- Number of participants
- 30
- Started
- 2025-11-11
- Last checked
- 2026-01
Plain English Summary
What is this study?
- • Testing a new treatment for functional cognitive disorder
- • NA - 30 participants
- • The goal of this study is to learn if a single session intervention for people with Functional Cognitive Disorder (FCD) is feasible and acceptable
Who can take part?
- • Ages 18 Years to 65 Years
- • Diagnosed with functional cognitive disorder
Where?
- • London - King's College Hospital
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
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.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 18 Years - 65 Years
- Who can join: All genders
What the study is looking for
- ✓Adults aged 65 or below
- ✓Not taking part in any other intervention study or trial
Who cannot take part
- ✗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)
See the full criteria
Where Is This Study? (1 UK site)
King's College Hospital
London, United Kingdom