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Brief Intervention for FCD: A Feasibility Study

K

King's College Hospital NHS Trust

Status

Enrolling

Conditions

Functional Cognitive Disorder

Treatments

Behavioral: Brief psychological intervention including attention training

Study type

Interventional

Funder types

Other

Identifiers

NCT07379723
IRAS Reference: 354504

Details and patient eligibility

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.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Intervention
Experimental group
Treatment:
Behavioral: Brief psychological intervention including attention training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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