Body Schema Alterations in Musculoskeletal Disorders : Effect of Laterality
NCT ID: NCT03567109
Last Updated: 2024-06-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
71 participants
OBSERVATIONAL
2018-07-13
2022-07-12
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of the Impact of Laterality on Cerebral Activation During a Motor Task of the Upper Limb in Healthy Subjects
NCT05428917
Evaluation of the Impact of Laterality on Brain Activation During a Virtual Mirror Therapy Task in Healthy Subjects
NCT05793762
Vestibular and Multisensory Influence on Bodily and Spatial Representations
NCT02072460
Combining Motor Imagery With Action Observation Does Not Lead to a Greater Autonomic Response Than Motor Imagery Alone During Simple and Functional Movements: a Randomized Controlled Trial.
NCT03232879
Rehabilitation Protocol for Disorders on Hand Sensitivity in Multiple Sclerosis Patients.
NCT01866878
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Shoulder rotator cuff tendinopathy
unilateral rotator cuff tendinopathy, 3 months or more duration, confirmed by imagery,
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
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
hand laterality judgment task
participants are asked to identify laterality of the hand presented on the screen
control
healthy subjects
hand laterality judgment task
participants are asked to identify laterality of the hand presented on the screen
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
hand laterality judgment task
participants are asked to identify laterality of the hand presented on the screen
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* social security affiliation
* signing consent
* rotator cuff tendinopathy, chronic low back pain, carpal tunnel syndrome or healthy subject
Exclusion Criteria
* psychiatric or neurological disorder
* psychotropic consumption
* previous experience with motor imagery
* bad french comprehension
* protected persons
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Angers
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CHU Angers
Angers, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2018-A00354-51
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.