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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NOT_YET_RECRUITING
160 participants
OBSERVATIONAL
2025-05-12
2027-03-27
Brief Summary
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Our primary objective is to compare pain levels and shoulder function one year after your initial consultation with your general practitioner for this episode. We also seek to assess which healthcare professionals you consult for your shoulder management, the treatments you receive (e.g., analgesics), and any imaging studies you undergo (if prescribed).
We will send you notifications to remind you of the survey completion schedule and provide the link to access the questionnaire.
Participation in this study requires your commitment and adherence to the timeline, as missing data may compromise the analysis of results.
Non-participation in the study will not affect your current medical care.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Primary care non-traumatic shoulder pain
Patients will be enrolled if they receive care in France for non-traumatic shoulder disorder, that is related to the rotator cuff.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Consultation with a general practitionner for this disorder in the 6 weeks prior to the inclusion
Exclusion Criteria
* Neurologic or rheumatismal shoulder disorder
* Frozen shoulder (current or past)
* History of advanced glenohumeral athritis
* History of shoulder surgery (on the affected side)
18 Years
ALL
No
Sponsors
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Conseil National de l'Ordre des Masseur Kinésithérapeutes (CNOMK)
UNKNOWN
GIRCI Auvergne Rhône-Alpes
UNKNOWN
University Hospital, Grenoble
OTHER
Responsible Party
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Principal Investigators
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Thomas LATHIERE, PT, PhDc
Role: PRINCIPAL_INVESTIGATOR
Grenoble Alpes University Hospital
Central Contacts
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Other Identifiers
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2024-A01019-38
Identifier Type: -
Identifier Source: org_study_id
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