Validation of the Dutch version of the Hip Outcome Score
Completed
- Conditions
- hip painimpingement hip10023213
- Registration Number
- NL-OMON47747
- Lead Sponsor
- Reinier de Graaf Groep
- Brief Summary
Trial ended prematurely
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 136
Inclusion Criteria
Patients who:
- are 18-65 years of age
- have physical examination and radiological examination suspect for FAI
- Inclusion will not interfere with standard care for FAI
- provided informed consent
- understand the Dutch language
Exclusion Criteria
Patients who:
- have had prior surgery to the hip for FAI
- have pathological fracture or other metastatic pathology
- refuse to particpatie
- do not speak the Dutch language
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary endpoints are internal consistency, reliability, construct validity<br /><br>and content validity of the Dutch version of the HOS.</p><br>
- Secondary Outcome Measures
Name Time Method <p>The secondary endpoints are the smallest detectable change (SDC) and the<br /><br>minimal clinical important difference (MCID), 6 months postoperatively.</p><br>