跳至主要内容
临床试验/NCT04068454
NCT04068454进行中(未招募)不适用

The Use of Virtual Reality in Shoulder Reeducation : Interests and Limits.

University of Liege2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2019年2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
进行中(未招募)
入组人数
50
试验地点
2
主要终点
Score of Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire

研究概览

简要总结

The objective of this study is to assess the interest and the efficiency of virtual reality in functional rehabilitation of shoulder pain and shoulder injuries. Participants will follow a 12-week rehabilitation program based either on exercises or on a program integrating virtual reality. Results obtained with classical rehabilitation will be compared with the one obtained virtual reality.

详细描述

Fifty people will be included in the study. Then, they were randomly separated in two groups : 25 people will do the "classical rehabilitation" and the other 25 will have a treatment with virtual reality.

Each group (virtual reality and "classical rehabilitation") is going to follow 12 weeks of rehabilitation, at a rate of 2x 30 minutes per week. In "virtual reality group", each session will be divided in two parts : 15 minutes of virtual reality exercises and 15 minutes of exercises from "classical program". Exercises suggested in the classical program have been chosen among evidence based exercises described in literature.

Before the beginning of rehabilitation sessions, participants will be assessed at the Laboratory of Human Motion Analysis of the University of Liege. At this place, EMG activity of periscapular muscles (upper trapezius, lower trapezius and serratus anterior) (Delsys Trigno) , 3D scapular kinematics (Codamotion) will be assessed on the painful side when doing shoulder elevations in sagittal and in frontal planes. Maximum isometric strength will also be assessed using handheld dynamometer (MicroFet2) in 3 different positions (SeatedU90°, SeatedU125°, Prone-v-thumbs up)

This first evaluation will be done after the 12 week of rehabilitation too, with the same method.

Participants will also have to complete Dash (Disability of the Arm, Shoulder and Hand) questionnaire 3 times during the study (at the beginning, at 6 weeks and at the end of the study). Moreover, pain score will be asked to participants at each rehabilitation session.

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
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

classical rehabilitation group

Active Comparator

干预措施: EBM rehabilitation exercises (Other)

virtual reality group

Experimental

干预措施: Virtual reality device (Device)

结局指标

主要结局

Score of Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire

时间窗: change from baseline at 12 weeks

Functional ability and quality of life will be assessed using this questionnaire, with a maximal score of 100

次要结局

  • 3D scapular motion(Change from baseline at 12 weeks)
  • Maximum voluntary isometric contraction(Change from baseline at 12 weeks)
  • Shoulder pain(change from baseline at 12 weeks)
  • EMG activity(Change from baseline at 12 weeks)

研究者

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

Camille Tooth

Principal Investigator

University of Liege

研究点 (2)

Loading locations...

相似试验