Return to sport after ACL replacement surgery: can a sensor for function-based follow-up with reproducible biofeedback improve outpatient rehabilitation after knee injuries?

Not Applicable

Conditions: S83.53

Registration Number: DRKS00024359

Lead Sponsor: Arcus Kliniken

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 80

Inclusion Criteria

acute unilateral rupture of the anterior cruciate ligament
- Indication for surgical reconstruction (arthroscopic, semitendinosus-gracilis tendoplasty)
- Participants are capable of giving consent, have full legal capacity and understand the nature, extent, significance and consequences of the examination
- Rupture and surgery less than 6 months

Exclusion Criteria

- bucket handle lesion of a meniscus
- cartilage damage >ICRS II
- complete second ligament injury with indication for intervention
- multi-ligament injury
- Rupture and surgery more than 6 months apart
- Neurological damage and underlying disease
- Pre-operations on the lower extremities
- Pregnancy
- Underlying rheumatic disease
- Non-compliance

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Validation of the Orthelligent system related to the subjective IKDC (International Knee Documentation Committee) after 3 months.

Secondary Outcome Measures

Name	Time	Method
Validation of the Orthelligent system related to subjective IKDC after 6 months.<br><br>Equivalence or superiority of sensor-assisted post-treatment compared to standard therapy, related to subjective IKDC and sensor-assisted function test after 3,6 and 12 months.<br><br><br>Function, pain level, quality of life, return to work, return to sport.