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Developing a machine-based training program in rehabilitation after reconstruction of the anterior cruciate ligament

Not Applicable
Recruiting
Conditions
Anterior cruciate ligament tear.
Sprain of anterior cruciate ligament of knee
Registration Number
IRCT20191013045090N1
Lead Sponsor
Tarbiat Modares University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
20
Inclusion Criteria

Unilateral ACL injury with specialist physician diagnosis and MRI approval
At least 3 months after ACL reconstruction surgery (With Bone-Patellar-Tendon-Bone Surgery Type)
Male
Full consent to participate in the research
Having a referral from an orthopedic specialist
Complete cardiovascular health of patients with physician approval
Balanced state of mind

Exclusion Criteria

Unfinished treatment programs and assessment
The occurrence of any sudden systemic disorder during rehabilitation according to the patient
The patient's willingness to withdraw from the study and unfinished treatment
Performing exercises outside the prescribed schedule according to the patient
Receive any treatment other than the treatment plans prescribed in this research plan
Injury to other ligaments and knee joint structures with orthopedic specialist approval
Previous surgery or injury in the knee of the opposite side and other joints of the lower extremities with orthopedic specialist approval
Taking painkillers, anti-inflammatory drugs, etc
Chronic illness or other known condition that may affect research research

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Static Balance. Timepoint: Pre and Post Intervention. Method of measurement: Balance Error Scoring System ?Test.;Dynamic Balance. Timepoint: Pre and Post Intervention. Method of measurement: Modified Star Excursion Balance Test.;Physical Function. Timepoint: Pre and Post Intervention. Method of measurement: Single leg hop for time & One leg hop for distance.
Secondary Outcome Measures
NameTimeMethod
Pain Intensity. Timepoint: Pre and Post Intervention. Method of measurement: Visual Analogue Scale.;Knee range of motion. Timepoint: Pre and Post Intervention. Method of measurement: Goniometery.;Thigh Atrophy. Timepoint: Pre and Post Intervention. Method of measurement: Measurement of thigh circumference with Cm tape measure.
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