orthopedische klacht (surmenage, patellofemorale pijn) patellofemoral pain syndrome
Conditions
Interventions
None listed
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: cases: patellofemoral pain for at least 3 months and minimum pijn score (VAS 3/10) controls: no complaints or surgery in the past (in the leg)
Exclusion criteria
Exclusion criteria: cases and controls: specific knee disorders like meniscus or ligament injury (e.g. ACL)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main outcome measures are changes in oxygenated hemoglobine concentrations (O2Hb), deoxygenated hemoglobine concentrations (HHb), total hemoglobine (THb) and tissue saturation index (TSI). Those parameters will be determined in two protocols, with protocol 1 simulating prolonged sitting and protocol 2 simulating descending stairs. Differences in changes between healthy subjects and patients with PFP will be investigated. | — |
Secondary
| Measure | Time frame |
|---|---|
| Anterior Knee Pain Scale * Dutch Version (AKPS-DV), 13 item questionnaire Tegner Score, 10 item level of physical activity blood pressure prepatellair skinfold thickness measured with Harpenden skinfold caliper patella width measured with caliper Decline step-down test (DSDT) measuring pain-free flexion angle Lower limb range of motion (LLROM) measuring soft tissue flexibility of the kinetic chain Visual Analogue Scale (VAS) measuring pain intensity while performing protocol 1 and 2 | — |
Countries
Netherlands
Outcome results
None listed