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临床试验/NCT05269303
NCT05269303已完成不适用

Optimizing the Health-related Functions of a Wearable Monitoring Device in the Daily Life of Community-dwelling Older Adults: A Randomized Pilot Study

The Hong Kong Polytechnic University1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2022年7月10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
72
试验地点
1
主要终点
The change of use intention of wearable monitoring device

研究概览

简要总结

The aim is to implement an intervention program to promote the continued use of Wearable Monitoring Devices among older adults through a peer support approach facilitating the incorporation of Wearable Monitoring Devices in daily life.

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)

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
  • own a smartphone
  • able to communicate in Cantonese or Mandarin
  • able to access the Internet at home or elsewhere

排除标准

  • have a confirmed diagnosis of cognitive impairment
  • bed-bound
  • currently own a wearable monitoring device
  • have already engaged in other wearable device studies

结局指标

主要结局

The change of use intention of wearable monitoring device

时间窗: Data collection will be conducted at the 1-month (T1), 3-month (T2), and 6-month (T3) time points

It will be measured using a 4-item, 5-point Likert scale adopted from Bhattacherjee (2001) and Windasari et al. (2021). The five-point scale ranges from 1 = not at all satisfied to 5 = very certain, with higher scores representing a higher chance of continuing to use the WMD.

次要结局

  • The change of health service utilization among baseline (T0) and at the 1-month (T1), 3-month (T2), and 6-month (T3) time points(baseline (T0) and at the 1-month (T1), 3-month (T2), and 6-month (T3) time points)
  • The change of adherence rate of wearing wearable monitoring device(Data collection will be conducted at the 1-month (T1), 3-month (T2), and 6-month (T3) time points)
  • The change in quality of life among baseline (T0) and at the 1-month (T1), 3-month (T2), and 6-month (T3) time points(baseline (T0) and at the 1-month (T1), 3-month (T2), and 6-month (T3) time points)
  • Recruitment rate(baseline pre-intervention)
  • Incidence of reports of adverse events(6-month (T3) time points)
  • Incidence of reports of technical difficulties(6-month (T3) time points)
  • Attrition rate(6-month (T3) time points)
  • The change of perceived usability of the wearable monitoring device before and after the program(baseline pre-intervention, 6-month (T3) time points)

研究者

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

Arkers, Wong

Assistant professor

The Hong Kong Polytechnic University

研究点 (1)

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