dysfunctions in the lower extremity (knee) (pain, reduced range of motion...) Healthy volunteers
Conditions
Interventions
Group 1: In one measurement session, two assessment procedures are conducted for all participants. The results of these assessments are compared. The participants get no intervention.
Sponsors
Professur für Konservative und Rehabilitative Orthopädie, Technische Universität München
Eligibility
Sex/Gender
All
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: We include participants (m/f/d) between 18 and 40 years with current dysfunctions in the lower extremity (knee).
Exclusion criteria
Exclusion criteria: Participants are excluded if they suffer from current musculoskeletal pain in the shoulder girdle, the neck or the elbows as well as from other nonspecific musculoskeletal disorders, e.g. fibromyalgia or any rheumatic disorder. In addition, participants are excluded if they are pregnant, in the nursing period, diagnosed with any neurological disorder or take medication that affects perception or proprioception.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary aim of our study is to estimate the proportion of patients with dysfunctions (evaluated via Bunkie Test), who also show a positive comparison test (isokinetic measurement) as well as the sensitivity of the Bunkie Test The following outcome measurements are conducted therefore: 1. isokinetic measurement: Hcon/Qcon ratio 2. Bunkie Test: Performance in seconds Both assessments are evaluated in a single 60-minute measurement procedure | — |
Countries
Germany
Contacts
Public ContactAnna Gabriel
Professur für Konservative und Rehabilitative Orthopädie, Technische Universität München
Outcome results
None listed