Traduction and Validation of the Central Sentitization Inventory Into French
NCT ID: NCT02270775
Last Updated: 2014-10-21
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
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UNKNOWN
150 participants
OBSERVATIONAL
2014-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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Fibromyalgia Patients
The central Sensitization questionnaire will be filled in by each patients included.
After One week, patients will filled it the questionnaire again to study the reliability.
No interventions assigned to this group
Ankle sprain Patients
The central Sensitization questionnaire will be filled in by each patients included.
No interventions assigned to this group
Healthy Volunteers
The central Sensitization questionnaire will be filled in by each volunteer included.
After One week, volunteers will filled it the questionnaire again to study the reliability.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Clinical Diagnosis of a Acute of Subacute Ankle Spain (Group 2)
* Healthy Volunteer (Group 3)
Exclusion Criteria
18 Years
65 Years
ALL
Yes
Sponsors
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Cliniques universitaires Saint-Luc- Université Catholique de Louvain
OTHER
Responsible Party
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Locations
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Cliniques Universitaires Saint-Luc
Brussels, Brussels Capital, Belgium
Countries
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Other Identifiers
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CSI-French
Identifier Type: -
Identifier Source: org_study_id
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