Virtual Reality in Reeducation : Application to Shoulder Affections
The Use of Virtual Reality in Shoulder Reeducation : Interests and Limits.
1 other identifier
interventional
50
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2019
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2019
CompletedFirst Submitted
Initial submission to the registry
March 21, 2019
CompletedFirst Posted
Study publicly available on registry
August 28, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2024
CompletedNovember 29, 2023
November 1, 2023
5.6 years
March 21, 2019
November 28, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Score of Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire
Functional ability and quality of life will be assessed using this questionnaire, with a maximal score of 100
change from baseline at 12 weeks
Secondary Outcomes (4)
Shoulder pain
change from baseline at 12 weeks
EMG activity
Change from baseline at 12 weeks
3D scapular motion
Change from baseline at 12 weeks
Maximum voluntary isometric contraction
Change from baseline at 12 weeks
Study Arms (2)
classical rehabilitation group
ACTIVE COMPARATORvirtual reality group
EXPERIMENTALInterventions
Functional exercises will be done by virtual reality group
Eligibility Criteria
You may qualify if:
- unilateral scapular dyskinesis
- positive scapular assistance test and positive resistance test
- shoulder pain
- ability to play sport despite shoulder pain
- one or more positive tendinous tests
You may not qualify if:
- traumatic history of shoulder injury in the last 6 months
- surgical history at shoulder or cervical location
- scoliosis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Liege
Liège, Liège, 4000, Belgium
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Camille Tooth
University of Liege
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 21, 2019
First Posted
August 28, 2019
Study Start
February 1, 2019
Primary Completion
August 30, 2024
Study Completion
August 31, 2024
Last Updated
November 29, 2023
Record last verified: 2023-11
Data Sharing
- IPD Sharing
- Will not share