跳至主要内容
临床试验/NCT03463122
NCT03463122已完成不适用

Virtual Reality Based Visual Perception Evaluation and Rehabilitation-pilot Study

National Rehabilitation Center, Seoul, Korea2 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2014年8月1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
发起方
入组人数
56
试验地点
2
主要终点
Change in Field of regard-response time

研究概览

简要总结

Head-mounted display based virtual reality rehabilitation for hemispatial neglect.

详细描述

The investigators examine about the efficacy of field-of-regard-focused visual exploration therapy implemented using a head-mounted display virtual reality system for hemispatial neglect rehabilitation following stroke.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • presence of left hemispatial neglect as demonstrated by a score above the cut-off on the line bisection test or star cancellation test of the Behavioral Inattention Test, or mild-to-moderate neglect-related functional impairment defined by a score of 1-20 points on the Catherine Bergego Scale
  • age 19 to 65 years
  • first-time right hemispheric ischemic or haemorrhagic stroke as evidenced by brain imaging and medical records
  • a score >25 on the Mini-Mental State Examination

排除标准

  • presence of oculomotor palsies or visual defects as assessed via standard neurological examination
  • orthopaedic disorders affecting neck movement
  • inability to maintain a seated position.

研究组 & 干预措施

Training first

Other

This group completed 20 sessions of a field of regard-focused visual exploration therapy program using an head mount display (five daily sessions per week over a period of four weeks) in addition to conventional therapy followed by four weeks of conventional therapy

干预措施: field of regard-focused visual exploration therapy (Device)

Training first

Other

This group completed 20 sessions of a field of regard-focused visual exploration therapy program using an head mount display (five daily sessions per week over a period of four weeks) in addition to conventional therapy followed by four weeks of conventional therapy

干预措施: conventional therapy (Other)

Waiting first

Other

This group completed four weeks of conventional therapy followed by 20 sessions of a field of regard-focused visual exploration therapy program using an head mount display (five daily sessions per week over a period of four weeks) in addition to conventional therapy.

干预措施: field of regard-focused visual exploration therapy (Device)

Waiting first

Other

This group completed four weeks of conventional therapy followed by 20 sessions of a field of regard-focused visual exploration therapy program using an head mount display (five daily sessions per week over a period of four weeks) in addition to conventional therapy.

干预措施: conventional therapy (Other)

结局指标

主要结局

Change in Field of regard-response time

时间窗: Baseline, 4 weeks from baseline, 8 weeks from baseline

time interval between target onset and response with field of regard setting

Change in Field of regard-success rate

时间窗: Baseline, 4 weeks from baseline, 8 weeks from baseline

percentage of correct responses (clicking the left or right mouse button in response to a blue or red target, respectively) with field of regard setting

Change in Field of regard-head movement

时间窗: Baseline, 4 weeks from baseline, 8 weeks from baseline

sum of all quantified head-rotations with field of regard setting

次要结局

  • Field of view-response time(Baseline, 4 weeks from baseline, 8 weeks from baseline)
  • Field of view-success rate(Baseline, 4 weeks from baseline, 8 weeks from baseline)
  • Line bisection test(Baseline, 4 weeks from baseline, 8 weeks from baseline)
  • Star cancellation test(Baseline, 4 weeks from baseline, 8 weeks from baseline)
  • Catherine Bergego Scale(Baseline, 4 weeks from baseline, 8 weeks from baseline)

研究者

发起方
National Rehabilitation Center, Seoul, Korea
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Joon-Ho Shin

Team manager of Department of Neurorehabilitation

National Rehabilitation Center, Seoul, Korea

研究点 (2)

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