跳至主要内容
临床试验/NCT06401564
NCT06401564招募中不适用

Improving Functional and Cognitive Outcomes After Ischemic Stroke Using Virtual Reality Based Rehabilitation

Stony Brook University2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2023年4月17日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
15
试验地点
2
主要终点
Simulator sickness questionnaire

研究概览

简要总结

Use the template below as a guide to write a brief study description in plain language. Tailor the text that appears in brackets and yellow to your research study. To finalize, delete the text in italics.

The goal of this single-arm study is to explore the use of early virtual reality-based rehabilitation as an adjunct to conventional physical/occupational therapy in adult patients with acute ischemic stroke. The main question it aims to answer is:

Feasibility and tolerability of using immersive Virtual Reality technology-based therapy for patients suffering from acute ischemic stroke in an inpatient hospital setting Participants will receive 1 or 2 virtual reality therapy sessions and complete surveys at the end of each session.

研究设计

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

  • Age > 18
  • MRI or CT imaging confirmed ischemic stroke
  • Able to follow multistep commands

排除标准

  • Plegia in both arms
  • Previous reported history of vertigo or inner ear dysfunction
  • Patients with epilepsy
  • Patients who cannot begin therapy during admission
  • Patients who are pregnant
  • Patients with a pre-existing condition that interferes with virtual reality usage (e.g., visual impairment, limitation of either upper extremity or neck).

结局指标

主要结局

Simulator sickness questionnaire

时间窗: After each session up to 5 weeks

An evaluation tool for assessing the subjective severity of simulator sickness symptoms. A 16-item questionnaire evaluating different symptoms on a scale from 0 (not at all) to 4 (severe).

Feasibility survey

时间窗: After each session up to 5 weeks

The User Satisfaction Evaluation Questionnaire (USEQ) is a 14-item questionnaire evaluating satisfaction on a scale from 1 (not at all) to 5 (severely).

次要结局

  • NIHSS(Hospital discharge, an average of 7 days)
  • Modified Rankin Scale (mRS)(Hospital discharge, an average of 7 days)
  • Duration of sessions(After each session up to 1 week)
  • Adverse events(After each session up to 5 weeks)
  • Time spent by therapist(After each session up to 1 week)

研究者

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

Jason Mathew

Assistant Professor

Stony Brook University

研究点 (2)

Loading locations...

相似试验