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临床试验/NCT06645132
NCT06645132进行中(未招募)不适用

Pilot Study to Understand the Feasibility of Implementing a Wearable Device Cueing System Following Bone Marrow Transplant

Medical College of Wisconsin2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2024年10月28日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
15
试验地点
2
主要终点
Pilot evaluation of intervention efficacy

研究概览

简要总结

The purpose of this study is to pilot test the feasibility of providing patients diagnosed with a hematologic malignancy, undergoing an allogeneic bone marrow transplant, a wearable device and smartphone app (similar to a Fitbit), that would send personalized reminders to move during their post-transplant inpatient hospital stay to promote physical recovery and well-being.

详细描述

Enrolled patients who have been diagnosed with a hematologic malignancy and are scheduled to undergo an allogeneic bone marrow transplant will use a custom-designed wearable device and smartphone application as a behavioral intervention to cue exercise. Participants will be asked to wear the wearable device for the duration of their post-transplant inpatient hospital stay.

Aim 1. To examine the potential efficacy of the wearable device + smartphone application to prompt alloBMT patients to move.

Aim 2. To receive participant feedback on their experience participating in the study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
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

入选标准

  • At least 18 years of age
  • Diagnosed with hematologic malignancy
  • Scheduled to receive an alloBMT
  • Physician consent to participate in the study

排除标准

  • Inability to complete 15 minutes walking unassisted

结局指标

主要结局

Pilot evaluation of intervention efficacy

时间窗: cumulative percent from day 1 through discharge from hospital, on average day 30

Efficacy will be evaluated by examining the percentage of time participants responded to the cued exercise prompts.

Patient feedback from participation in the study

时间窗: day 10

Patient experience will be evaluated by looking at the central tendencies of the ratings from the post-participation evaluation survey.

次要结局

未报告次要终点

研究者

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

Whitney Morelli

Principal Investigator

Medical College of Wisconsin

研究点 (2)

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