Effect of rehabilitation treatment in dynamic valgus of lower limb

Effect of comprehensive rehabilitation treatment on pain, muscle force, physical function and quality of life in officer students with dynamic valgus of the lower limb

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200825048523N1

Enrollment

Registered

2022-11-17

Start date

2023-01-21

Completion date

Unknown

Last updated

2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Genu Valgum (Knock knee). Valgus deformity, not elsewhere classified, knee

Interventions

Intervention 1: Intervention group: knee strengthening exercises (specific strengthening of vastus medialis oblique muscle), hip strengthening exercises (specific strengthening of hip abductor and ext

Eligibility

Sex/Gender

Male

Age

18 Years to 30 Years

Inclusion criteria

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

Exclusion criteria: Trauma to knee Injury to anterior cruciate ligament

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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.

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Secondary

Measure	Time frame
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.	—

Measure

Time frame

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.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaeed Mikaili

Shahid Beheshti University of Medical Sciences

saeed.mikaely@yahoo.com+98 21 8863 1084

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026