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临床试验/NCT04556591
NCT04556591已完成不适用

Mobile Technology and Data Analytics to Identify Real-time Predictors of Caregiver Well-Being

University of Michigan1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2020年11月5日最近更新:
适应症
干预措施

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
Feasibility and Acceptability as Measured by the Percentage of Agree or Strongly Agree Responses to the Individual Items on the Feasibility Questionnaire

研究概览

简要总结

The purpose of this study is to test whether personalized messages from an easy-to-use mobile app improve mood and stress among care partners and to see if care partners like using the app.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • •Care Partner Inclusion Criteria:
  • •Provide emotional, physical, and/or financial support/assistance to an individual with spinal cord injury (SCI), Huntington's Disease (HD), or hematopoietic cell transplantation (HCT)
  • •Have access to necessary resources for participating in a technology-based intervention (smartphone/tablet and internet access) and be willing to use their personal equipment/internet for this study, including downloading the study app and the Fitbit® app on their mobile device
  • •Care partners of persons with HD: Be caring for an adult (18 years or older) with a clinical diagnosis of HD
  • •Care partners of persons with SCI: Be caring for an adult (18 years or older) that is ≥1 post-injury and sustained a medically documented SCI at age 16 or older
  • •Care partners of persons with HCT: Be caring for an adult (18 years or older) who is receiving, has received or is scheduled to receive HCT

排除标准

  • •Is a professional, paid caregiver (e.g., home health aide)

研究组 & 干预措施

Control

Active Comparator

Participants will wear the Fitbit® and provide daily reports of health related quality of life (HRQOL) over a three-month (90 day) period (without the personalized feedback).

干预措施: Control (Behavioral)

Just-in-time adaptive intervention (JITAI)

Experimental

Participants will wear the Fitbit®, provide daily reports of health related quality of life (HRQOL) and receive personalized pushes over a three-month (90 day) period.

干预措施: Just-in-time adaptive intervention (JITAI) (Behavioral)

结局指标

主要结局

Feasibility and Acceptability as Measured by the Percentage of Agree or Strongly Agree Responses to the Individual Items on the Feasibility Questionnaire

时间窗: 3 months of wearing the Fitbit and completing the surveys

Items are scaled from 1 to 5 to indicate the level of agreement, where "1" indicates "strong disagreement" and "5" indicates "strong agreement". Percentages shown are the combined percentage of participants who selected "agree" or "strongly agree" or their equivalent (as labeled).

次要结局

  • Attrition as Measured by the Percent of Participants Completing the Study(3 months of wearing the Fitbit and completing the surveys)
  • Adherence as Measured by the Percentage of Contributed Data Over the Course of the Study(3 months of wearing the Fitbit and completing the surveys)

研究者

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

Noelle E Carlozzi

Associate Professor of Physical Medicine and Rehabilitation

University of Michigan

研究点 (1)

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