D66 D67
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Adult diagnosed with moderate and severe haemophilia A or B. - age = 18 years
Exclusion criteria
Exclusion criteria: - Suffering from other bleeding diseases outside of haemophilia - any invasive joint therapies (e.g., radiosynoviorthesis) or surgeries (e.g., TEP or arthrodesis) up to 6 months before the examination date - acute analgesic drug intake outside of the patient’s regular treatment regime 12 hours before the examination.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the convergent construct validity: The validity of the TUG is assessed by correlating the results of the TUG (time in seconds) with those of the already validated "Haemophilia Joint Health Score" (a test to assess joint health; score range 0-124), and with an established objective clinical test measuring the same construct, namely the Short Physical Performance Battery (SPPB), which includes the 5-time sit to stand test and the 4-meter walk test; score range 0-12). Additionally, the results are correlated with subjective measures of physical function and mobility, including the Haemophilia Activity List (HAL; score range 0-100), the Haemophilia and Exercise Project-Test-Questionnaire (HEP-Test-Q; score range 0-100), and subjective weekly physical activity time (time in minutes per week). | — |
Secondary
| Measure | Time frame |
|---|---|
| - Test-Retest Reliability - Inter-Rater Reliability - Discriminant (known groups) construct validity - Standard error of measurement - Minimum detectable change | — |
Countries
Germany
Contacts
Bergische Universität Wuppertal, Lehrstuhl für Sportmedizin