跳至主要内容
临床试验/NCT05667480
NCT05667480进行中(未招募)不适用

Utilization of Immersive Virtual Reality in Computerized Script Training for People with Aphasia: a Feasibility Study

The Hong Kong Polytechnic University2 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2023年4月10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
26
试验地点
2
主要终点
Percentage correct in reading aloud the sentences included in the trained scripts

研究概览

简要总结

The goal of this intervention study is to investigate the effects of immersive virtual reality in rehabilitation of language and communication of individuals with post-stroke aphasia. The main research questions are:

  1. Is VR-based script training a feasible treatment to Cantonese-speaking PWA?
  2. Will VR-based script training, when compared to conventional script training, better enhance treatment outcomes in functional communication of PWA?

Participants will be assessed before, in the middle of, immediately after treatment and 8-week post treatment in terms of their performance on:

  1. Accuracy and time for producing trained scripts.
  2. Accuracy and time for producing un-trained scripts
  3. Standardized aphasia test on severity of language impairment
  4. Standardized aphasia test on functional communication

The participants will be randomly allocated to receive one of the treatment:

  1. Virtual reality-based computerized script training; or
  2. Computerized script training without virtual reality Researchers will compare the treatment outcomes of the two treatment conditions and see if treatment with virtual reality would better promote outcomes when compared to training without virtual reality.

研究设计

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

入排标准

年龄范围
30 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • a stroke onset more than six months, with an Aphasia Quotient (AQ) below 96.4, as evaluated by the Cantonese version of Western Aphasia Battery (CAB; Yiu, 1992),
  • premorbid fluent Cantonese speakers,
  • aged between 30 and 80 years,
  • no reported progressive neurogenic disorders such as dementia or Parkinson's disease,
  • no motor speech disorders of moderate to severe level, and
  • normal or corrected-to-normal vision and hearing functions

排除标准

  • concurrent participation in other aphasia treatment trials, and
  • incompatibility with immersive VR exposure such as complains of nausea, headache, or other severe discomforts during trial use of a head-mounted device during screening.

结局指标

主要结局

Percentage correct in reading aloud the sentences included in the trained scripts

时间窗: From baseline up to 1-week post training

Trained scripts will be shown in written form while the PWA will be asked to read aloud the scripts.

Time required in read aloud of trained scripts

时间窗: From baseline up to 1-week post training

Total time to read aloud the trained scripts

Percentage correct in spontaneous production of the sentences included in the trained scripts

时间窗: From baseline up to 1-week post training

No written cue will be provided while the PWA will produce the scripts upon questions.

Time required for spantaneous production of trained scripts

时间窗: From baseline up to 1-week post training

No written cue will be provided while the PWA will produce the scripts upon questions.

次要结局

  • CAB(From baseline up to 1-week post training)
  • Percentage correct in producing untrained but related scripts(From baseline up to 1-week post training)
  • CANELT(From baseline up to 1-week post training)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验