跳至主要内容
临床试验/NCT03750526
NCT03750526招募中不适用

Investigate the Effectiveness of Augmented Reality and Repetitive Transcranial Magnetic Stimulation Technology in Persons With Stroke

Taipei Medical University Hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2018年7月31日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Change of Time Up Go test (TUG)

研究概览

简要总结

This study is to investigate the combined effects of repetitive Transcranial Magnetic Stimulation (rTMS) and Augmented Reality (AR) intervention on cortical excitability, balance, gait, activity in individuals with stroke. Forty participants will be recruited in this study. They will be allocated to four group: rTMS and AR group (10), sham rTMS and AR group (10), AR group (10), and conventional physiotherapy group (10).

详细描述

Participants will be randomized allocated to four groups: rTMS and AR group, sham rTMS and AR group, AR group ,and conventional physiotherapy group in current study. All participants underwent four weeks, 3 sessions per week, and 60 minutes per session training program. Motor evoked potential (MEP), Time up go test (TUG), Berg Balance Scale (BBS), Fugl-Meyer Assessment (FMA), Multi-directional Reach Test (MDRT),The Postural Assessment Scale for Stroke Patients (PASS), and Taiwanese Depression Questionnaires (TDQ) will be assessed before and after intervention in all participants.

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
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Cognitive ability is sufficient to understand the nature of study (Mini-Mental State Examination score was above 23).
  • •Participants suffer from unilateral hemiplegia caused by a first-ever stroke.
  • •Participants are stable in medical and psychological condition.

排除标准

  • •Participants have other neurologic problems that can affect balance and walking ability.
  • •Participants take of drugs or have other medical condition that can affect balance and function.
  • •Participants have contraindications for rTMS intervention such as pacemaker, cochlear implants, metal in the brain or skull, open wound of brain, or history of epilepsy.

研究组 & 干预措施

rTMS and AR group

Experimental

Ten participants in group A will undergo repetitive transcranial magnetic stimulation (real, 1 Hz, 15 minutes), follow by a session of augmented reality exercise (45 minutes), 3 days per week for 4 weeks.

干预措施: rTMS and AR (Behavioral)

Sham rTMS and AR group

Active Comparator

Ten participants in group B will receive repetitive transcranial magnetic stimulation (sham,1 Hz, 15 minutes), follow by a session of augmented reality exercise (45 minutes), 3 days per week for 4 weeks.

干预措施: Sham rTMS and AR (Behavioral)

AR group

Active Comparator

Ten participants in group C will undergo augmented reality exercise 60 minutes a day and 3 days per week for four weeks.

干预措施: AR (Behavioral)

Conventional physiotherapy group

Active Comparator

Ten participants allocated to the group D will receive conventional physiotherapy 60 minutes a day and 3 days per week for four weeks.

干预措施: Conventional physiotherapy (Behavioral)

结局指标

主要结局

Change of Time Up Go test (TUG)

时间窗: Measurement before and after intervention ( week 0 and at the end of week 4) in four groups

The TUG test will ask participants to stand up, walk for 3 m, turn, walk back and sit down as fast as they can during the test, and the time requires for each patient to complete the test is recorded.

次要结局

  • Change of Berg Balance Scale (BBS)(Measurement before and after intervention ( week 0 and at the end of week 4) in four groups)
  • Change of Motor evoked potential (MEP)(Measurement before and after intervention ( week 0 and at the end of week 4) in four groups)
  • Change of Fugl-Meyer Assessment (FMA)-Lower extremity(Measurement before and after intervention ( week 0 and at the end of week 4) in four groups)
  • Change of Multi-directional Reach Test (MDRT)(Measurement before and after intervention ( week 0 and at the end of week 4) in four groups)
  • Change of The Postural Assessment Scale for Stroke Patients (PASS)(Measurement before and after intervention ( week 0 and at the end of week 4) in four groups)
  • Change of Taiwanese Depression Questionnaires (TDQ)(Measurement before and after intervention ( week 0 and at the end of week 4) in four groups)

研究者

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

Lai chien hung

Professor

Taipei Medical University Hospital

研究点 (1)

Loading locations...

相似试验