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Randomized Controlled ACL Injury Prevention Study

Randomized Controlled ACL Injury Prevention Study - Randomized Controlled ACL Injury Prevention Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON33770
Enrollment
60
Registered
2009-12-15
Start date
2009-09-01
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

orthopedische aandoening anterior cruciate ligament injury

Interventions

Subjects will undergo a dynamic visual feedback intervention.

Sponsors

Rijksuniversiteit Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) Subjects must be between 18 years or older 2) Subjects with no history of major lower extremity injury or surgery 3) Subjects with no current or recent (6 months) injury to the entire lower extremity 4) Playing soccer in the NBB "Rayon Noord Hoofdklasse* 5) Currently able to participate in training and games for 100%

Exclusion criteria

Exclusion criteria: 1) Subjects with insulin dependent diabetes mellitus, rheumatologic disorder, cerebral vascular disorder, or any other central or peripheral disease that might interfere with sensory input 2) Previous history of cardiovascular or pulmonary disease 3) Uncontrolled metabolic disorder 4) Subjects with previous compartment syndrome or any vascular conditions to their lower leg 5) Subjects with any pain with maximal muscle contractions 6) Subjects with any skin irritations or abrasion and/or any history of allergy to adhesive tape 7) Subjects with any known central and/or peripheral nervous system disorders 8) Subjects with any known current lower extremity injury (eg. fracture, meniscal, ACL, posterior cruciate ligament, medial collateral ligament or lateral collateral ligament injury) 9) Subjects with previous history of major lower extremity injury (eg. fracture) or surgery

Design outcomes

Primary

MeasureTime frame
Kinematic and kinetic data of the hip, knee and ankle and EMG activity of the quadriceps, hamstrings and gastrocnemius.

Secondary

MeasureTime frame
History on injuries and / or surgeries Activity between intervention and follow up tests Tegner activity level questionnaire

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)