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临床试验/NCT07638462
NCT07638462招募中不适用

RIsEStroke (Recovery Insights Into Early Mobility Post Stroke)

Wake Forest University Health Sciences1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年7月8日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
1

研究概览

简要总结

This study is designed to better understand how patients with severe stroke move during their hospital stay. It will track their activity using a small wearable device (activPAL) along with standard mobility information already collected in clinical care. The goal is to learn what typical movement patterns look like early after a stroke and how well patients meet mobility goals while in the hospital. What is learned from this study may allow determination of how treatment for stroke patients may be improved to improve patient long-term mobility.

详细描述

Acute Ischemic Stroke (AIS) is a leading cause of disability and death in the United States. However rehabilitation after stroke has shown to reduce the risk of medical and neurological complications and improved brain recovery. There has been extensive research on early mobilization and advanced therapy after AIS in low to moderate stroke severity patients. There has been little research in the mobility of severe AIS patients.

Research studies have utilized several different devices to track movement of subjects. The activPAL device has been used extensively in research studies in a variety of diseases and age groups. The activPAL4pro provides data on posture, limb movement, sleep, sitting and ambulatory movement. For this reason, the activPAL4pro device will be utilized to provide extensive data on our AIS patients.

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

  • Adults aged 18 years and older
  • Hospitalized patients with acute ischemic stroke
  • Initial National Institutes of Health Stroke Scale (NIHSS) score of 10 or greater
  • Baseline modified Rankin Scale (mRS) score of 0-2
  • Current modified Rankin Scale (mRS) score of 3-5

排除标准

  • Current or expected End-of-life discussions
  • Current plans for surgical intervention
  • Patients with pre-mRS of 3-5
  • Patients with orthopedic, musculoskeletal, integumentary injury that would prevent safe weight bearing, mobility or equipment use
  • Uncontrolled cardiorespiratory dysfunction or disease
  • Active/uncontrolled seizures
  • Isolation status that would prevent mobility outside of the room
  • Weight that exceeds the safe limits of mobility equipment

研究组 & 干预措施

Severe Acute Ischemic Stroke Patients

Experimental

Hospitalized adult patients with severe acute ischemic stroke who are observed prospectively for mobility patterns during hospitalization using the activPAL4pro device and routine clinical mobility assessments.

干预措施: activPAL device (Device)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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RIsE Stroke Mobility Study | 临床试验