- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03358160
Motor Representations in Orthopedic Patients
Motor Representations in Orthopedic Patients: Pilot Studies
The aim of this study is to investigate the possible effects that a motor limitation at the peripheral level might have on the ability to visually discriminate others' actions.
Previous literature has shown that specific motor skills (motor expertise) facilitate the visual discrimination of domain-specific actions, and that these motor experts' superior abilities might be mediated by areas not only responsible for the visual recognition of movements (as it happens in non-expert subjects) but also involved in motor planning. Similarly, impairment in the motor system due to neurological damage modulates not only the ability to perform movements but also the ability to discriminate and predict the temporal course of observed actions.
Based on these findings, it has been hypothesized that the motor representations of gait, despite being a hyper-learned motor pattern, might be subjected to modification as a result of an impairment of walking caused by a peripheral functional limitation in the lower limbs as the one characterizing orthopaedic patients who underwent a surgical operation for total knee arthroprosthesis. In this protocol, patients are thus required to perform visual discrimination tasks based on the observation of movements performed with either the upper or lower limbs, and their performance is expected to correlated with their functional impairments in movement execution.
These results would indicate that the (in)ability to perform a movement might have an impact on its representation at the central level and on internal motion simulation capabilities, which also influence the ability to visual discriminate others' actions through action-perception transfer: this would suggest that rehabilitation in orthopaedic patients should take into account (and restore) such a central impairment in motor representations.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
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Milan, Italy, 20161
- Recruiting
- IRCCS Galeazzi Orthopedic Hospital
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Principal Investigator:
- Eraldo Paulesu, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Participants must be able to understand instructions and have no history of neurological or psychiatric disorders.
Exclusion Criteria:
- History of neurological or psychiatric disorders.
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
TKA
Orthopaedic patients who underwent surgical operation for total knee arthroprothesis.
|
The investigators will compare the groups' performance during action discrimination tasks related to movements of the upper vs. lower limbs.
|
Rizoarthrosis
Orthopaedic patients who underwent surgical operation to treat chronic arthrosis of the thumb.
|
The investigators will compare the groups' performance during action discrimination tasks related to movements of the upper vs. lower limbs.
|
Healthy Controls
Healthy age-matched controls.
|
The investigators will compare the groups' performance during action discrimination tasks related to movements of the upper vs. lower limbs.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Group Differences in action discrimination performance.
Time Frame: End 2018.
|
Group Differences in action discrimination performance depending on the impairment in movement execution.
|
End 2018.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RMPO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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