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临床试验/NCT07379723
NCT07379723招募中不适用

Feasibility Pilot Study of a Brief Intervention in Functional Cognitive Disorder

King's College Hospital NHS Trust1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年11月11日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
30
试验地点
1
主要终点
Participant recruitment, feasibility and retention from baseline to follow-up

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

研究组 & 干预措施

Intervention

Experimental

干预措施: Brief psychological intervention including attention training (Behavioral)

结局指标

主要结局

Participant recruitment, feasibility and retention from baseline to follow-up

时间窗: From enrollment to follow-up 6 weeks post-intervention.

• Number of participants recruited and retention rate (number and percentage of participants completing post-intervention measures) will be recorded.

次要结局

  • Acceptability of the study intervention at follow-up(Post-intervention follow-up at 6 weeks.)
  • Change in symptoms of depression from enrolment to post-intervention follow-up(At enrolment and at follow-up 6 weeks post-intervention)
  • Change in symptoms of anxiety from enrolment to post-intervention follow-up(At enrolment and at follow-up 6 weeks post-intervention)
  • Change in functional impairment from enrolment to post-intervention follow-up(At enrolment and at follow-up 6 weeks post-intervention)
  • Change in quality of life from enrolment to post-intervention follow-up(At enrolment and at follow-up 6 weeks post-intervention)
  • Change in self-reported cognitive symptoms from enrolment to post-intervention follow-up(At enrolment and at follow-up 6 weeks post-intervention)

研究者

发起方
King's College Hospital NHS Trust
申办方类型
Other
责任方
Sponsor

研究点 (1)

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