Prevention of anterior cruciate ligament injuries
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Healthy female and male participants (2) Untrained (no strength training on regular basis during the last year)
Exclusion criteria
Exclusion criteria: (1) Metal-containing or electrically conductive objects in the body (e.g., spiral, solid braces, clips, vessel clips, pacemakers or joint prostheses). (2) Injuries of the anterior cruciate ligament or other ligaments, menisci, cartilage of the knee joint (3) Regular smokers (4) Cachexia or obesity (BMI 30 kg/m²). (5) Active or suspected infection (6) Severe heart failure and COPD or a high risk of thrombosis (7) Acute spinal disease (e.g., lumboischialgia, disc prolapse, spinal stenosis). (8) Severe joint, muscular or systemic diseases (9) Neurological diseases affecting cognition (10) Manifest tumour or other severe chronical diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome of this study is the alteration of the anterior cruciate ligament volume. It is measured before and after the intervention period (16 weeks) using magnetic resonance imaging (MRI). | — |
Secondary
| Measure | Time frame |
|---|---|
| Additional outcomes measured before and after the intervention period are: muscle volume (MRI) and maximal voluntary muscle strength of the thigh muscles (by means of dynamometry) as well as the maximal muscle activity during this maximum voluntary contraction (by means of electromyography). | — |
Countries
Germany
Contacts
Forschungslabor für Biomechanik und Implantattechnologie, Orthopädische Klinik und Poliklinik, Universitätsmedizin Rostock