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临床试验/NCT04168463
NCT04168463已完成不适用

Exploring Use of Companion Robot Pets for Older Adults in Care Homes, an 8-month Stepped-wedge, Cluster Randomised Control Trial.

University of Plymouth2 个研究点 分布在 1 个国家目标入组 83 人开始时间: 2020年1月1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
83
试验地点
2
主要终点
Neuropsychiatric Inventory (Nursing Home Version) (Cummings, 1994)

研究概览

简要总结

This study will assess the use and impact of the affordable 'Joy for All' robot pets for older people with and without dementia living in the care homes in South West England.

Robot pets such as Paro have shown potential in improving wellbeing (including reduced agitation, loneliness, medication use, anxiety and depression), however previous work conducted by the investigators suggests Paro is less acceptable to older adults than alternative devices; the Joy for All cat and dog. Paro is also much more expensive (£5000 compared to £100) limiting its use within the real world, and limiting the number of people able to benefit.

The investigators therefore wish to explore the potential of these more affordable robots in achieving wellbeing benefits.

详细描述

This study will be an eight month stepped-wedge, cluster randomised control trial exploring the use and impact of 'Joy for All' robot pets with older people living in care homes in South West England. Participants will include individuals with and without dementia.

The study aims to:

  • See if affordable robot pets lead to improved wellbeing and are robust and engaging over 4-8 months in care homes and nursing homes.
  • Identify under what circumstances, for which care home residents, and with what impact the robot pets are used.

The wellbeing outcomes to be explored include; neuropsychiatric symptoms, challenging behaviour, communication and loneliness.

Additional outcomes include monitoring of medication use, 1:1 care applications, and maintenance of a usage chart.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

盲法说明

N/A not possible

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

  • Any resident at a collaborating care home or nursing home that has consent to participate.

排除标准

  • Any resident at a collaborating home without consent to participate.

结局指标

主要结局

Neuropsychiatric Inventory (Nursing Home Version) (Cummings, 1994)

时间窗: Measured at baseline, 4 months and 8 months

Will be used to assess any changes in neuropsychiatric symptoms of care home residents. For each domain, there are four scores; frequency (0-4, with higher scores being most frequent), severity (0-3, with higher scores being most severe), total score (frequency x severity), and caregiver distress (0-5, higher scores signal more distress)

次要结局

  • Challenging Behaviour Scale (Moniz-Cook et al., 2001)(Measured at baseline, 4 months and 8 months)
  • Campaign to End Loneliness Measurement Tool (3-item) (Campaign to End Loneliness, n.d.)(Measured at baseline, 4 months and 8 months)
  • Holden Communication Scale (Strøm et al., 2016)(Measured at baseline, 4 months and 8 months)
  • Medication Use Review(Will be reviewed for the 4 weeks prior to study commencement, 4 weeks prior to 4 month post study commencement and the 4 weeks prior to study completion at 8 months)
  • 1:1 Care Applications(Will be reviewed for the 4 weeks prior to study commencement, 4 weeks prior to 4 month post study commencement and the 4 weeks prior to study completion at 8 months)
  • Qualitative Impact Review(Dairies will be maintained during intervention phases (8 months for cluster 1, 4 months for cluster 2), interviews and summative review will be conducted at 8 months)

研究者

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

Hannah Bradwell

Principal Investigator

University of Plymouth

研究点 (2)

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