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The Effect of McKenzie exercises in treatment of anterior knee pain

Comparing the effect of exercise therapy with Mckenzie versus Common methods in treatment of patients with Anterior Knee Pain (AKP): A randomized controlled trial.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150314021459N5
Enrollment
22
Registered
2018-02-13
Start date
2017-07-03
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Condition 1: Anterior Knee Pain. Condition 2: anterior knee pain. Other disorders of the musculoskeletal system and connective tissue

Interventions

Intervention2: First the subjects have physiotherapy including hot pack with defined TENS. The place for electrodes are according to acupuncture points. Therapeutic exercise includes strengthening of

Sponsors

Vice chancellor for Research and Technology, Iran University of Medical Sciences,
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 40 Years

Inclusion criteria

Inclusion criteria: Their age is between 16 and 40 years old. Have at least two months pain in front of knee. The pain rate is at least 3 cm by virtue of linear Visual Analog Scale. At least 2 of the questionnaire Kujala give a positive response.

Exclusion criteria

Exclusion criteria: Dissatisfaction of patient in each step of the study Having a history of real locking of the knee Having a history of dislocation of the patella. Having the joint inflammation. Having active infections The presence of any abnormalities in knee joint radiography Having the ligament injuries. Having the malignancy. Having the actual length difference of the lower extremities. Taking of any tranquilizer medication during the 48 hours before the evaluation. The presence of any abnormalities in the chest, upper and lower extremities. The previous history of physiotherapy for knee.

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: At the beginning of the study, 10 days and one month after the start of the study. Method of measurement: Linear scale VAS.;Function. Timepoint: At the beginning of the study, 10 days and one month after the start of the study. Method of measurement: Kujala questionnaire.;Range of motion of knee. Timepoint: At the beginning of the study, 10 days and one month after the start of the study. Method of measurement: Goniometer.

Secondary

MeasureTime frame
Lenght of the hamstring muscles. Timepoint: At the beginning of the study, 10 days and one month after the start of the study. Method of measurement: Clinometer.;Lenght of the quadriceps muscle. Timepoint: At the beginning of the study, 10 days and one month after the start of the study. Method of measurement: Clinometer.;Hamstring muscle strenght. Timepoint: At the beginning of the study, 10 days and one month after the start of the study. Method of measurement: Hand Dynamometer.;Quadriceps muscle strenght. Timepoint: At the beginning of the study, 10 days and one month after the start of the study. Method of measurement: Hand Dynamometer.;The fear avoidance beliefs. Timepoint: At the beginning of the study, 10 days and one month after the start of the study. Method of measurement: FABQ questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMojtaba Kamyab

Vice research, School of Rehabilitation Sciences, Iran University of Medical Sciences

kamyab@iums.ac.ir+98 21 2225 8769

Outcome results

None listed

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