A real-time biofeedback device for measuring active knee extension range after anterior cruciate ligament reconstruction surgery- An exploratory study
Phase 2
- Conditions
- Health Condition 1: S835- Sprain of cruciate ligament of knee
- Registration Number
- CTRI/2022/09/045297
- Lead Sponsor
- Marwadi University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Subjects who underwent ACL reconstruction surgery
Nineteen years of age or older, with the ability to provide their own consent and have access to a smartphone
Exclusion Criteria
1.History of surgery or traumatic injury to the uninvolved lowernextremity
2.Complication after ACL reconstruction surgery
3.Significant neurologic impairments
4.More than 1 surgery for the treatment of torn AC
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Active Knee extension range of motion in degrees using a real-time biofeedback device <br/ ><br>2. Active and passive Knee range of motion in degrees using universal goniometer.Timepoint: 0-4 weeks
- Secondary Outcome Measures
Name Time Method 1.Visual Analogue Scale (VAS) <br/ ><br>2.International Knee Documentation Committee (IKDC) <br/ ><br>Subjective Knee Evaluation Form.IKDC-SKFTimepoint: 0-4 weeks