Status:
COMPLETED
The Effectıveness Of Structured Myofascial Chain Exercise Training After Anterior Cruciate Ligament Reconstruction
Lead Sponsor:
Bahçeşehir University
Collaborating Sponsors:
Istanbul University - Cerrahpasa
Conditions:
Anterior Cruciate Ligament Injuries
Anterior Cruciate Ligament Rupture
Eligibility:
All Genders
18-45 years
Phase:
NA
Brief Summary
Anterior cruciate ligament reconstruction(ACLR) surgery accepts best choices which condicions are totaly ruptured ACL or partial ruputures when patients with high activity level. Rehabilitation after ...
Eligibility Criteria
Inclusion
- Being between the ages of 18-45
- Being able to establish written and verbal communication in Turkish
- Post-Op rehabilitation after primary ACL surgery with Autograft in reconstruction, at 8 weeks, post op at 12 weeks at the latest.
- To have participated in an exercise-based rehabilitation program structured by a physiotherapist in the early and mid-term after surgery (a standardized program will not be applied in the early and mid-term, and participation in the study after rehabilitation is sufficient)
- Gaining full range of motion in the knee joint in the direction of extension, gaining full range of motion in the flexion direction with a maximum loss of 5 degrees
- BMI greater than 20 and less than 30
- No previous history of surgery involving the lower extremity
- To be able to perform a normal gait pattern without compensatory movements
- m.Quadriceps Femoris Muscle strength of at least 60% of the healthy side
- Having an IKDC score of 55 or higher
- To have sufficient technological device usage skills and fast internet infrastructure to use video communication technologies without any problems.
- Having a device that provides the necessary equipment for video calling
- Having 15 m2 of space to allow exercise in the living area
Exclusion
- Using allograft in reconstruction
- History of any chronic systemic, rheumatological, neurological, vascular disease
- History of traumatic injury to intact extremities and trunk in the last 6 months
- Presence of pain complaints including spine and shoulder pain over 3 according to the Visual Analogue Scale
- Those who use anti-inflammatory drugs
- Presence of cognitive or psychological illness that will prevent cooperation
Key Trial Info
Start Date :
January 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 15 2023
Estimated Enrollment :
52 Patients enrolled
Trial Details
Trial ID
NCT05423184
Start Date
January 1 2022
End Date
August 15 2023
Last Update
September 25 2023
Active Locations (1)
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1
Istanbul University-Cerrahpasa
Istanbul, Turkey (Türkiye)