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临床试验/NCT06222554
NCT06222554已完成不适用

Pilot/Feasibility Study Examining the Use of a Novel Immersive Motion Tracking Upper Extremity Exercise Program for Acute Hospitalized Patients

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2024年8月6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
12
试验地点
1
主要终点
Number of Adverse Events

研究概览

简要总结

The objective of this study is to evaluate the feasibility of the MoveMend Health software program as an integrated supplement to traditional acute care/in-hospital occupational therapy for patients following liver and kidney transplants, as determined by recruitment rates, program completion, intervention adherence, safety incidence, and patient feedback on device/program performance.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Device Feasibility
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
否

入选标准

  • •English speaking (software program is currently only available in English)
  • •Status post kidney or liver transplant this admission
  • •Physician orders for occupational therapy evaluation and treatment
  • •Orientation Log > 25
  • •Negative for delirium per the Confusion Assessment Method

排除标准

  • •Orthopedic or surgical precautions that limits shoulder range of motion beyond 90 degrees
  • •Upper extremity hemiplegia with inability to lift upper extremity against gravity
  • •Accommodation code of Intensive Care Unit

研究组 & 干预措施

Patients Hospitalized following Kidney or Liver Transplant

Experimental

Patients in the study will be introduced to the exercise software program and provided with a demonstration. Measurements will be taken at baseline (post-operation) and at the final study visit. Participants will remain in the study until the end of their hospital stay, typically no longer than 6 months post-operation.

干预措施: MoveMend Health (Device)

结局指标

主要结局

Number of Adverse Events

时间窗: Up to Month 6 Post-Operation

Measured using data from participant's electronic medical record.

Percentage of Participants who Adhere to Intervention

时间窗: Up to Month 6 Post-Operation

Measured by session duration and frequency, as recorded by the device. Participants will be classified as "adhering" or "not adhering."

Recruitment Rate

时间窗: Up to Month 6 Post-Operation

Calculated by dividing the number of participants enrolled by the total number of patients contacted or screened.

Percentage of Participants who Complete Exercise Program

时间窗: Up to Month 6 Post-Operation

Percentage of enrolled participants who complete the interventional program.

次要结局

  • Change in EuroQol 5-Dimension 5-Level (EQ-5D-5L) Questionnaire Index Score(Baseline, End of Hospital Stay (typically no more than 6 months post-operation))
  • Change in Activity Measure for Post-Acute Care (AMPAC) Score(Baseline, End of Hospital Stay (typically no more than 6 months post-operation))
  • Upper Extremity Range of Motion (ROM) Change(Baseline, End of Hospital Stay (typically no more than 6 months post-operation))
  • Change in Grip Strength(Baseline, End of Hospital Stay (typically no more than 6 months post-operation))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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