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临床试验/NCT03937297
NCT03937297已完成不适用

A Culturally Appropriate Multimodal Non-pharmacological Intervention for Chinese People With Mild-to-Moderate Dementia

The University of Hong Kong1 个研究点 分布在 1 个国家目标入组 216 人开始时间: 2019年4月23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
216
试验地点
1
主要终点
Changes in cognitive performance

研究概览

简要总结

This is a mixed-methods research that includes a single-blind three-arms randomized control trials and a focus group study. The quantitative study aims to investigate the additional clinical benefits of the Six Arts intervention over an evidence-based non-pharmacological intervention translated from western culture, cognitive stimulation therapy (CST). The qualitative part aims to explore the acceptance and understanding of family caregiver of the Six Arts intervention and CST.

It is hypothesized that 1) the group who have received Six Arts intervention would show superior quality of life; 2) both Six Arts and CST groups would show superior cognitive improvement compared with usual care; 3) the Six Arts group would show greater improvement in behavioral and neuropsychological symptoms and functioning compared with the groups receiving CST or usual care.

详细描述

Dementia is a disabling chronic condition affecting over 47 million people worldwide. Chinese population will be one of the main driver in the increasing trend in dementia prevalence. Accumulating evidence suggests effectiveness of certain non-drug interventions in maintaining cognition and quality of life in people with mild-to-moderate dementia, such as cognitive stimulation therapy (CST). These interventions are designed and tested in western populations with issues of cultural adaptation when applied in Chinese. Culturally appropriate and effective interventions for Chinese people with mild-to-moderate dementia are lacking.

The Six Arts stem from ancient Confucian philosophy, which promotes behaviours that can impact on multiple mind-body functional domains. These domains correspond to social, physical, and cognitive activities with theoretical basis and empirical evidence of benefits in cognition, functioning, and quality of life. Using the Six Arts as a cultural framework, a group-based multimodal intervention has been developed in Hong Kong for Chinese people with mild-to-moderate dementia.

The study will recruit 240 people with mild-to-moderate dementia in a randomized single-blind controlled trial consisting of three groups: (1) Six Arts intervention; (2) CST; and (3) usual care. Neuropsychological and clinical assessments will be conducted at randomization (T0/baseline) and upon completion of the 24-session, twice-weekly intervention (T1/3 months), by an assessor unaware of group membership. Focus groups will be conducted after completion of the intervention in 60 family caregivers who have observed at least one session of the Six Arts intervention or CST.

This study will provide evidence on the effectiveness of two intervention protocols with potentials for large-scale implementation in the growing Chinese population with dementia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

The assessor would not be told if the participant is in the intervention or control group

入排标准

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

入选标准

  • aged 60 or above
  • have clinical diagnosis of dementia or a Clinical Dementia Rating (CDR) of 1-2 suggestive of mild-to-moderate disease;
  • able to communicate and understand communication, see and hear well enough to participate in a meaningful assessment;
  • person with dementia and/or his/her caregiver can provide informed consent

排除标准

  • suffering from major physical illness or disability that affect participation;
  • had experience with the 24-session of CST or Six Arts intervention protocols
  • Caregivers (for the focus group study)
  • Inclusion Criteria:
  • provide care to the person of dementia for more than 8 hours per week
  • have observed at least one intervention session of either CST or Six Arts intervention

结局指标

主要结局

Changes in cognitive performance

时间窗: T0 (baseline), T1 (up to 4 months)

measure by using the Alzheimer's Disease Assessment Scale - Cognitive section (ADAS-Cog), a standard cognitive test commonly used in clinical trials for people with dementia

Changes in quality of life of people with dementia

时间窗: T0 (baseline), T1 (up to 4 months)

measure by using a 13-item self-rating and proxy rating scale, the Quality of Life in Alzheimer's Disease (QoL-AD)

次要结局

  • CDAD(T0 (baseline), T1 (up to 4 months))
  • NPI-Q(T0 (baseline), T1 (up to 4 months))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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