Effect of rehabilitation treatment in dynamic valgus of lower limb

Not Applicable

Conditions: Genu Valgum (Knock knee).
Valgus deformity, not elsewhere classified, knee
M21.06

Registration Number: IRCT20200825048523N1

Lead Sponsor: Bagheiat-allah University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Pending

Sex: Male

Target Recruitment: 80

Inclusion Criteria

People with knee rotation syndrome along with valgus
Pain at least 3 score based on the numerical pain scale
Knee pain when running, jumping sitting, and standing up

Exclusion Criteria

Trauma to knee
Injury to anterior cruciate ligament

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain intensity. Timepoint: Measurement of pain intensity at the beginning of the study (before the intervention) and at the end of the study (6 weeks after the intervention). Method of measurement: Numerical pain rating scale.;Maximum muscle isometric contraction force. Timepoint: Measurement of maximum muscle isometric contraction force at the beginning of the study (before the intervention) and at the end of the study (6 weeks after the intervention). Method of measurement: Hand dynamo-meter.;Physical performance level. Timepoint: Measurement of physical performance level at the beginning of the study (before the intervention) and at the end of the study (6 weeks after the intervention). Method of measurement: Lower extremity functional scale.;Quality of life. Timepoint: Measurement of level of quality of life at the beginning of the study (before the intervention) and at the end of the study (6 weeks after the intervention). Method of measurement: 36-question quality of life questionnaire.

Secondary Outcome Measures

Name	Time	Method
Thickness and angle fibers of vastus medialis and leteralis oblique muscles. Timepoint: Measurement of thickness and angle of muscle fibers at the beginning of the study (before the intervention) and at the end of the study (6 weeks after the intervention). Method of measurement: Ultrasonography.;Joint distance of knee. Timepoint: Measurement of joint distance at the beginning of the study (before the intervention) and at the end of the study (6 weeks after the intervention). Method of measurement: Ultrasonography.