se of auditory feedback to improve a patients compliance with partial weight bearing
- Conditions
- Anterior cruciate ligament reconstruction
- Registration Number
- NL-OMON29061
- Lead Sponsor
- niversity Medical Center Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
Patients recovering from ACL reconstruction
- Younger than 65 years of age
Exclusion Criteria
- Significant orthopeadic disturbances or pain
- serious co-morbidities
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Percentage of incorrect steps: This parameter will be used to evaluate the difference in fractions of incorrect steps, with or without the use of the ABF device. <br /><br>2. Time interval between incorrect steps (exeeding either the maximum or minimum allowed weight): This parameter will be used to indicate the learning curve involved in adapting to the use of an ABF device.<br>
- Secondary Outcome Measures
Name Time Method An interview will be conducted after the seccond session, giving an indication of user acceptance of the auditory biofeedback training in general and the tested ABF device.