跳至主要内容
临床试验/NCT04630912
NCT04630912已完成不适用

Acceptance and Commitment Therapy (ACT) for People With Dementia Experiencing Psychological Distress: a Hermeneutic Single Case Efficacy Design (HSCED) Series

University of Nottingham1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2021年1月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
6
试验地点
1
主要终点
Change in anxiety

研究概览

简要总结

Introduction: People with dementia have a high prevalence of psychological distress but are under-served with evidence-based psychological interventions. To promote choice and improve clinical outcomes, there is a necessity to test different psychological intervention options for this population. Purpose: To investigate the effectiveness and acceptability of Acceptance and Commitment Therapy (ACT) for people with dementia, considering carer-supported, remote delivery and necessary therapy adaptations. Methods: A hermeneutic single case efficacy design (HSCED) series was used to analyse therapy process and change for three clients with dementia and psychological distress. Quantitative and qualitative data was collated ('rich case records') and analysed by three independent psychotherapy experts ('judges') who determined the outcome for each client. Results: Over the course of therapy, it was concluded that one client with dementia made positive changes, specifically reliable reductions in psychological distress, which were largely attributable to Acceptance and Commitment Therapy (ACT). Two clients remained unchanged. Discussion/Conclusion: Where change was achieved, the ACT-specific processes of values, committed action and acceptance, in combination with non-specific therapy factors including a strong client-carer relationship, existing client interests and individualised therapy adaptations, were facilitative of change. Hence, ACT may be feasible and effective by helping carers to better meet the needs of their loved ones with dementia. Future research to optimise ACT delivery in this population may be beneficial. Furthermore, the assessment of carer factors (e.g., their psychological flexibility, the client-carer relationship) may strengthen the evidence-base for systemic ACT-use.

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
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Inclusion criteria for people with dementia
  • Participants were included in the study if they had:
  • A clinical diagnosis of dementia (any type)
  • A clinically significant level of psychological distress (a score of ≥8 on the GAD-7 and ≥10 on the PHQ-9).
  • Ability to give informed consent
  • Inclusion criteria for caregiver of person with dementia
  • Participants were included in the study if they:
  • Cared for someone with a clinical diagnosis of dementia (any type)
  • Were paid or unpaid and regularly supported them with activities of daily living
  • Aged 18+ (no maximum age limit)
  • Able to give informed consent

排除标准

  • Exclusion criteria for people with dementia
  • Participants were excluded if they:
  • Were already receiving psychotherapy
  • Had insufficient English or language abilities to engage in therapy
  • Were unable to consent to and/or engage in therapy
  • Exclusion criteria for caregiver of person with dementia
  • Participants were excluded if they:
  • Had insufficient English or language abilities to support the person with dementia or engage in study/Change Interviews
  • Were unable to consent to and/or engage in study

结局指标

主要结局

Change in anxiety

时间窗: Through study completion, up to 24 weeks

Generalised anxiety disorder questionnaire (GAD-7), scored 0-21, where higher scores indicate a greater severity of anxiety.

Change in depression

时间窗: Through study completion, up to 24 weeks

Patient health questionnaire (PHQ-9), scored 0-27, where higher scores indicate a greater severity of depression.

次要结局

  • Change in psychological flexibility(Through study completion, up to 24 weeks)
  • Change in wellbeing(Through study completion, up to 24 weeks)
  • Change in client problems(Through study completion, up to 24 weeks)
  • Change in therapeutic alliance(Through study completion, up to 12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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