Schem-TMS: Body Schema Alterations in Musculoskeletal Disorders : Effect of Laterality

Sponsor
University Hospital, Angers (Other)
Overall Status
Unknown status
CT.gov ID
NCT03567109
Collaborator
(none)
120
1
11.2
10.7

Study Details

Study Description

Brief Summary

This study assess ocular movements in a hand laterality judgment task in a population of musculoskeletal disorders. Reaction time, error rate and visual strategy are compared between musculoskeletal disorders and healthy patients, and between the different locations of the disorder.

Condition or Disease Intervention/Treatment Phase
  • Other: hand laterality judgment task

Detailed Description

Musculoskeletal disorders are a major public health issue. Recent studies showed that body schema alterations are involved in the chronification of those disorders. Those alterations bring the opportunity for new exploration or therapeutic solutions. Our hypothesis is that musculoskeletal disorders lead to motor imagery alterations relative to body schema disorders. Reaction time extension et error rate increase in a hand laterality judgment task would confirm that hypothesis. It is assumed that body schema alterations of patients suffering from musculoskeletal disorders could change with localisation, dependant on disorder's laterality and distality.

It is a monocentric, prospective, case-control trial, with 4 subgroups of 30 patients :

shoulder rotator cuff tendinopathy, carpal tunnel syndrome, chronic low back pain, healthy subjects. We compare reaction time and error rate on a hand laterality judgement task. In that task, participants are asked to identify hand right or left laterality, when those hand is presented on a computer screen, by answering with the keyboard. Hands are shown on palmar or dorsal view and with 12 different angles of rotation. An eye-tracking device register participant eye movements during the task.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
120 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Body Schema Alterations in Patients Suffering From Musculoskeletal Disorders. Does Disorder Laterality Influence Recruitment of Cerebral Areas Involved in Voluntary Motricity?
Actual Study Start Date :
May 24, 2018
Anticipated Primary Completion Date :
Nov 1, 2018
Anticipated Study Completion Date :
May 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Shoulder rotator cuff tendinopathy

unilateral rotator cuff tendinopathy, 3 months or more duration, confirmed by imagery,

Other: hand laterality judgment task
participants are asked to identify laterality of the hand presented on the screen

chronic low back pain

non specific chronic (3 months) low back pain

Other: hand laterality judgment task
participants are asked to identify laterality of the hand presented on the screen

carpal tunnel syndrome

unilateral carpal tunnel syndrome, confirmed by electromyogram, 3 months or more duration

Other: hand laterality judgment task
participants are asked to identify laterality of the hand presented on the screen

control

healthy subjects

Other: hand laterality judgment task
participants are asked to identify laterality of the hand presented on the screen

Outcome Measures

Primary Outcome Measures

  1. error rate at the hand laterality judgment task [1 hour]

    number of errors divided by the total number of hands presented

  2. reaction time [1 hour]

    time to press on the keyboard the answer "Right" or "Left" after the hand was presented

Secondary Outcome Measures

  1. visual strategy [1 hour]

    assessment of the image's areas most fixed with the eyes

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • normal visual acuity

  • social security affiliation

  • signing consent

  • rotator cuff tendinopathy, chronic low back pain, carpal tunnel syndrome or healthy subject

Exclusion Criteria:
  • recent trauma or surgery

  • psychiatric or neurological disorder

  • psychotropic consumption

  • previous experience with motor imagery

  • bad french comprehension

  • protected persons

  • other painful affection than the inclusion criteria

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Angers Angers France 49100

Sponsors and Collaborators

  • University Hospital, Angers

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Angers
ClinicalTrials.gov Identifier:
NCT03567109
Other Study ID Numbers:
  • 2018-A00354-51
First Posted:
Jun 25, 2018
Last Update Posted:
Jun 25, 2018
Last Verified:
Jun 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 25, 2018