- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02326688
Quantification of Arm Non-Use After a Stroke
December 22, 2014 updated by: University Hospital, Montpellier
Reliability of Kinematic Analysis in Assessment and Rehabilitation of the Upper Arm of Stroke Patients Following a Cerebral Vascular Accident, Hemiparetic Subjects
Reproducibility assessment of a quantitative measure of the amount of trunk compensation by kinematic analysis in a grasping task in stroke patients.This "maladaptive trunk compensation" is suspected to be underlined by "arm non-use" in some patients, since this abnormal movement impairs the ability of patients to correctly flex their shoulder and extend their elbow during grasping.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
144
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Montpellier, France, 342095
- Recruiting
- UH Montpellier
-
Contact:
- isabelle laffont, md
- Phone Number: 0467338681
- Email: i-laffont@chu-montpellier.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
· Patient hemiparetic
- Hemiplegic Patient
- Patient can perform a global task with the gripping limb
Exclusion Criteria:
Patient can not actively tender elbow of the affected limb,
- Patient who can not actively flex the shoulder of the affected limb,
- Patient with a passive extension deficit elbow> 30 °,
- Patient with a shoulder flexion passive deficit> 60 °,
- Patient with severe neglect
- Patient bearer severe cognitive impairment
- A patient with aphasia understanding disorders
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: stroke patients
Kinematic measurement of the amount of trunk displacement during a grasping task
|
|
Experimental: control patients
Kinematic measurement of the amount of trunk displacement during a grasping task
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Kinematic measurement of trunk displacement by the maladaptive index trunk compensation
Time Frame: 1 day
|
The Maladaptive Index Trunk Compensation (MTC) is the difference between the compensation index (CI) in the free trunk condition and to the fixed core condition.
The compensation index is the core of the movement of the report on the movement of the hand.
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2014
Primary Completion (Anticipated)
December 1, 2016
Study Completion (Anticipated)
December 1, 2016
Study Registration Dates
First Submitted
December 15, 2014
First Submitted That Met QC Criteria
December 22, 2014
First Posted (Estimate)
December 29, 2014
Study Record Updates
Last Update Posted (Estimate)
December 29, 2014
Last Update Submitted That Met QC Criteria
December 22, 2014
Last Verified
December 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 9368
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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