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Clinical Trials/NCT02464293
NCT02464293CompletedNot Applicable

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

Lancaster University1 site in 1 country16 target enrollmentStarted: June 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
16
Locations
1
Primary Endpoint
depression at 3 months

Study Overview

Brief Summary

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.

Detailed Description

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •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

Exclusion Criteria

  • •Active suicidal intent

Arms & Interventions

mindfulness-based cognitive therapy

Experimental

Intervention: Mindfulness-based cognitive therapy (Other)

Outcomes

Primary Outcomes

depression at 3 months

Time Frame: 3 months post-intervention

Change in HADS depression score pre to 3 months post intervention

depression post intervention

Time Frame: 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

Time Frame: 1 year post-intervention

Change in HADS depression score pre to 1 year post intervention

Secondary Outcomes

  • anxiety at 3 months(3 months 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)
  • 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)
  • stress at 1 year(1 year post-intervention)
  • mindfulness at 1 year(1 year post-intervention)
  • sleep at 3 months(3 months 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)
  • 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)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr Jane Simpson

Research Director, Doctorate in Clinical Psychology

Lancaster University

Study Sites (1)

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