Assessment of the Safety and Performance of an Elbow Brace in the Prevention of Injuries During Sports Practice
- Conditions
- EpicondylitisTendonitis ElbowElbow Injury
- Interventions
- Device: Elbow SOFT 300Other: Control group
- Registration Number
- NCT05552235
- Lead Sponsor
- Decathlon SE
- Brief Summary
Decathlon has developed the Elbow soft300 which is a medical device that must be positioned around the elbow to keep a physical activity on a regular basis in case of chronic epicondylitis, pain associated with tendonitis or chronic instability.
The objective of this multicentre study is to collect data on the related clinical complications and clinical outcomes of market-approved Decathlon Elbow soft 300 product to demonstrate safety and performance of this device in a real-world setting.
Outcome data collected from this study will provide the basis for Post-Market Surveillance (PMS) reporting, Clinical Study Report (CSR), Clinical Evaluation Report (CER) on Decathlon ElbowSoft300 device and support peer-reviewed publications on products performance and safety.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 30
- Subject is aged ≥ 18 years old
- Subject has a chronic epicondylitis (>3 months) OR elbow pain associated with tendonitis OR chronic elbow instability (>3 months)
- The current condition of his/her elbow allows the subject to continue usual physical activity
- Subject has been informed and is willing to sign an informed consent form
- Subject is willing to comply with protocol requirements and return to the study center for all clinical evaluations and required follow-up (6 weeks)
- Subject is affiliated to the French social security regime
- Subject has conditions that may interfere with his/her ability to understand protocol requirements, participate in scheduled visits, or provide his/her informed consent
- Subject has worn a support (elbow brace or articulated orthosis) in the last month during his/her sport practice
- Subject has any medical condition that could impact the study at investigator's discretion
- Subject has a known hypersensitivity or allergy to the components of the device (polyamide, elastodiene, polyester, elastane)
- Adult subject to legal protection measure
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Orthosis group Elbow SOFT 300 Use of Elbow Soft 300 device during sport practice Control group Control group No medical device used during sport practice
- Primary Outcome Measures
Name Time Method Functionnal score Change from Baseline functionnal score at 6 weeks Comparison of the Patient Rated Elbow Evaluation (20-item questionnaire with a global score from 0=best outcome to 100=worst outcome) between the baseline and last follow-up visit in each group (orthosis vs control)
- Secondary Outcome Measures
Name Time Method Confidence level (confidence questionnaire related to physical activity) Change from Baseline confidence level at 6 weeks Gap in the confidence level related to physical activity (6-item questionnaire with a global score from 0=worst outcome to 100=best outcome), between the baseline and last follow-up visit in each group (orthosis vs control)
Safety (adverse events) 6 weeks of follow-up Comparison of adverse events rates between the groups (orthosis vs control)
Elbow pain Change from Baseline elbow pain at 6 weeks Comparison of elbow pain, assessed through a Numerical Rating Scale (NRS) ranging from 0=best outcome to 10=worst outcome, between the groups (orthosis vs control)
Elbow instability Change from Baseline elbow instability at 6 weeks Comparison of elbow instability, assessed through a Numerical Rating Scale (NRS) ranging from 0=best outcome to 10=worst outcome, between the groups (orthosis vs control)
Trial Locations
- Locations (2)
Centre Hospitalier de Boulogne-sur-Mer
🇫🇷Boulogne-sur-Mer, France
Centre Hospitalier Universitaire de Lille
🇫🇷Lille, France