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临床试验/ChiCTR1800015324
ChiCTR1800015324尚未招募Unknown

Combining mind body physical exercise, cognitive training, and nurse-led risk factor modification to enhance cognition among older adults with mild cognitive impairment: a pilot study

未提供1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2018年3月26日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
入组人数
30
试验地点
1
主要终点
feasibility of the intervention

研究概览

简要总结

The aim of this pilot study is to examine the feasibility of a complex intervention: cognitive training, mind body physical exercise, and nurse-led risk factor modification (CPR) on reducing cognitive decline among the older adults aged between 60 and 90 years with MCI when compared to health advice (HA) in primary care.

研究设计

研究类型
Interventional
主要目的
随机平行对照
盲法
The persons who conduct the assessments or data analyses will be blinded to group allocation.

入排标准

年龄范围
60 至 90(—)
性别
All

入选标准

  • for participants will be: (1) aged between 60 years and 90 years; (2) having Montreal Cognitive Assessment Hong Kong version (HK-MoCA) score within 19-21 after adjusting for years of educational (+1 point if < 6 years) suggesting MCI according to published research; and (3) being physically stable, as assessed by the study physician.

排除标准

  • for participants will be: (1) a diagnosis of dementia; (2) concurrent treatment with structured cognitive training, regular physical exercises including Tai Chi or other lifestyle modifications (e.g., diet) although no restrictions will be imposed on leisure activity; (3) a past history of bipolar affective disorder or psychosis; and (4) one or more significant communicative impairments. The use of psychotropic medication; this does NOT constitute an exclusion criterion, but any use of anti-dementia and other psychotropic medications should be kept on a stable dosage for at least three months before enrolment and also throughout the study.

研究组 & 干预措施

3

health advice control (HAC)

1

cognitive training, mind body physical exercise, and nurse-led risk factor modification (CPR)

2

risk factor modification (RFM)

结局指标

主要结局

feasibility of the intervention

时间窗: At 6 months

次要结局

  • The Chinese version of the Alzheimer’s Disease Assessment Scale - cognitive subscale (ADAS-Cog)(At baseline and 6 months)
  • CDR sum of box(At baseline and 6 months)
  • The Disability Assessment for Dementia (DAD)(At baseline and 6 months)
  • Quality of life (EQ5D)(At baseline and 6 months)
  • Depression and anxiety(At baseline and 6 months)
  • Cigarette smoking, alcohol drinking, diet and physical exercise(At baseline and 6 months)
  • Health service utilization(At baseline and 6 months)
  • Common diseases(At baseline and 6 months)
  • Demographic data(At baseline and 6 months)

研究者

发起方
未提供

研究点 (1)

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