Validation of Kujala German
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Purpose
The field of patellofemoral disorders and accordant therapeutical interventions is a high turnover research field. It is important to verify the clinical outcome with appropriate measuring tools. There is evidence that the Kujala score is a reliable and widely used measuring instrument of patellofemoral disorders. Indeed, the Kujala score was already used in many studies investigating patellofemoral disorders - also in german speaking patient groups. Unfortunately, we are not aware of a validated german version of the Kujala score. Other relevant knee outcome scores were already successfully translated into german language and validated by previous investigators.
So, it is the aim of our study to cross-culturally adapt and then to validate the Kujala score for use in German-speaking individuals with patellofemoral instability. It is hypothesized that the german version of the Kujala score shows:
- High divergent construct validity as determined by significant differences between patients and controls (hypothesis 1)
- High convergent construct validity as determined by significant correlations with other relevant scoring systems (hypothesis 2)
- High reliability (hypothesis 3)
- High responsiveness (hypothesis 4)
| Condition | Intervention |
|---|---|
|
Validation of Kujala Score German Version in Patients With Patellofemoral Instability and Scheduled MPFL-reconstruction |
Procedure: MPFL- Reconstruction |
| Study Type: | Observational |
| Study Design: | Observational Model: Case-Only Time Perspective: Prospective |
| Official Title: | Cross-cultural Adaptation and Validation of the German Version of the Kujala Score in Patients With Patellofemoral Instability - a Prospective Multi-centric Study |
- Kujala Score
- KOOS (Knee Injury and Osteoarthritis Outcome Score)
- Marx Activity Scale
- SF-12 (Short - Form 12)
- VAS pain
- Lysholm Score
| Study Start Date: | November 2011 |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| Patellofemoral Instability | Procedure: MPFL- Reconstruction |
Eligibility| Ages Eligible for Study: | 10 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Sampling Method: | Non-Probability Sample |
Patients with patellofemoral instability & scheduled MPFL-reconstruction
Inclusion Criteria:
- german speaking
- MPFL-reconstruction planed
Exclusion Criteria:
Contacts and Locations| Contact: Michael C Liebensteiner, MD, PhD | +43 512 504 80547 | michael.liebensteiner@i-med.ac.at |
| Austria | |
| Dept. Orthop. Surgery, Medical Univ. Innsbruck | Recruiting |
| Innsbruck, Tyrol, Austria, 6020 | |
| Contact: Martin Krismer, Prof. +43 512 504 22691 martin.krismer@uki.at | |
| Principal Investigator: Michael C Liebensteiner, MD, PhD | |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT01495507 History of Changes |
| Other Study ID Numbers: | Kuj-Germ-1 |
| Study First Received: | December 19, 2011 |
| Last Updated: | June 25, 2012 |
| Health Authority: | Austria: Ethikkommission |
ClinicalTrials.gov processed this record on June 17, 2013