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临床试验/NCT02464293
NCT02464293已完成不适用

A Pilot Evaluation of Mindfulness-based Cognitive Therapy for People With Huntington's Disease

Lancaster University1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2015年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
1
主要终点
depression at 3 months

研究概览

简要总结

This is a pilot study to see whether mindfulness-based cognitive therapy, which is a type of psychological therapy, is able to improve the psychological wellbeing of people who have the gene for Huntington's disease.

详细描述

Huntingdon's disease (HD) is a genetic neurodegenerative condition which causes problems with movement, coordination and cognitive functioning, and emotional difficulties are also commonly experienced. It is believed to affect around five to ten in 100,000 people of European descent, with recent UK estimates as high as 11.2-13.5. Each child of an affected person has a 50% chance of inheriting the condition. As age of diagnosis is typically around 35-55, with time from diagnosis to death around 20 years, those who are diagnosed have often seen their parents affected by the condition.

Many people at various stages of HD (including those who carry the gene but are pre-symptomatic) experience low mood, anxiety and other psychological difficulties. Indeed, alongside functional capacity, mood may be one of the main factors which contributes to health related quality of life, more so than discrete motor problems, or cognitive impairment. In addition, reports from patients suggest emotional and social concerns are important for individuals with the condition at the pre-symptomatic stage, and these concerns remain throughout the disease course. Medication may be effective to alleviate psychological difficulties for some people, but its efficacy has not been conclusively proven and it is not suitable for all. Psychological interventions may provide an alternative or additional way of alleviating distress.

Although it is commonly presumed that biological factors are the main determinants of psychological distress in people with HD, several studies have indicated that, while these may indeed be important, psychological factors are also significant. For example beliefs about the disease and coping mechanisms are associated with poorer mental health and higher levels of depression. Such psychological beliefs and coping patterns can be adaptively changed using psychological interventions, for example cognitive-based psychological therapies.

Little progress has been reported on the development of psychological interventions in HD despite the fact that people with HD have expressed an interest in psychological approaches and these are currently being successfully developed for people with other neurological conditions (e.g., in people with Parkinson's disease). It is therefore proposed to pilot mindfulness-based cognitive therapy (MBCT) which, although originally developed to help people with remitted depression from relapse, has been increasingly used to help people with current difficulties. It has also been piloted with people with Parkinson's disease who found it an acceptable intervention and reported improvements in self-management and psychological wellbeing. In general, MBCT has also recorded other gains including improved sleep quality and social functioning. It has also received sufficient evidence for it to be a recommended approach in the UK NICE guidelines for people with a history of depression. MBCT can also reduce anxiety and provides group support. There are also indications that mindfulness training can improve neurocognitive functioning, even in people with neurodegenerative disease. Finally, a psychological therapy subgroup within the European Huntington's Disease Network has recently been formed, thus indicating the rise of interest in psychological approaches and the timely nature of this work.

Hence this study will provide the first indication of whether MBCT, a therapeutic approach with an established evidence base, would be acceptable and useful for people with HD. In order to meet this aim, MBCT will be delivered to two groups, one to individuals who carry the gene but are pre-symptomatic and one to individuals who have begun to experience symptoms but are at an early stage of the disease course.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • For those with HD:
  • Patient at Manchester Centre for Genomic Medicine (UK)
  • All participants will have had genetic testing and shown to have the requisite CAG expansion on the huntingtin gene.
  • Participants must be pre-symptomatic or at stage 1 (still able to function at home and at work and handle financial affairs)
  • Clinical sign of depression (score on HADS of 7 or above)
  • No significant medication changes in 6 weeks prior to starting the course
  • For those who are relatives or friends of those with HD:
  • Must be a relative or friend of someone participating in the MBCT course

排除标准

  • Active suicidal intent

结局指标

主要结局

depression at 3 months

时间窗: 3 months post-intervention

Change in HADS depression score pre to 3 months post intervention

depression post intervention

时间窗: immediately post-intervention (up to two weeks afterwards)

Change in Hospital Anxiety and Depression Scale (HADS) depression score pre to post intervention (People with HD only)

depression at 1 year

时间窗: 1 year post-intervention

Change in HADS depression score pre to 1 year post intervention

次要结局

  • anxiety mid-course(4 weeks after start of intervention)
  • anxiety post intervention(immediately post-intervention (up to two weeks afterwards))
  • stress mid course(4 weeks after start of intervention)
  • sleep at 3 months(3 months post-intervention)
  • stress at 1 year(1 year post-intervention)
  • mindfulness at 1 year(1 year post-intervention)
  • relationship satisfaction at 1 year(1 year post-intervention)
  • depression mid-course(4 weeks after start of intervention)
  • anxiety at 1 year(1 year post-intervention)
  • sleep at 1 year(1 year post-intervention)
  • anxiety at 3 months(3 months post-intervention)
  • stress post intervention(immediately post-intervention (up to two weeks afterwards))
  • stress at 3 months(3 months post-intervention)
  • quality of life post intervention(immediately post-intervention (up to two weeks afterwards))
  • quality of life at 3 months(3 months post-intervention)
  • quality of life at 1 year(1 year post-intervention)
  • positive affect at 1 year(1 year post-intervention)
  • coping at 3 months(3 months post-intervention)
  • carer burden at 1 year(1 year post-intervention)
  • mindfulness mid-course(4 weeks after start of intervention)
  • mindfulness post intervention(immediately post-intervention (up to two weeks afterwards))
  • mindfulness at 3 months(3 months post-intervention)
  • sleep post intervention(immediately post-intervention (up to two weeks afterwards))
  • positive affect post intervention(immediately post-intervention (up to two weeks afterwards))
  • coping post intervention(immediately post-intervention (up to two weeks afterwards))
  • coping at 1 year(1 year post-intervention)
  • relationship satisfaction at 3 months(3 months post-intervention)
  • positive affect at 3 months(3 months post-intervention)
  • carer burden at 3 months(3 months post-intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Jane Simpson

Research Director, Doctorate in Clinical Psychology

Lancaster University

研究点 (1)

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