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The effect of kinesiotyping on reaction time in anterior cruciate ligament surgery

The effect of kinesiotyping on reaction time in people with anterior cruciate ligament tear surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221030056342N5
Enrollment
30
Registered
2024-11-06
Start date
2024-12-30
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Rupture of the anterior cruciate ligament. Sprain of anterior cruciate ligament of unspecified knee

Interventions

Intervention 1: Intervention group: In the intervention group (kinesiotype), an English Y-shaped kinesiotype will be connected from the origin of the rectus femoris with a tension of 25 to 30% to its

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Unilateral damage Anterior cruciate ligament tear with or without meniscal tear confirmed by MRI and orthopedics. Six months have passed since the ligament reconstruction operation and the patient has received rehabilitation during this period.

Exclusion criteria

Exclusion criteria: People with knee cartilage damage such as osteoarthritis People with injuries and tears of the posterior and lateral medial and lateral ligaments History of back pain in the last six months Any pathological deviation in the knee, including genovarum and genovalgoma Feeling any pain and discomfort in the knee that the pain scale is more than two. Because pain can affect posture control as a confounding variable. Consumption of sedatives or alcohol up to 48 hours before treatment, history of dizziness, fainting, nausea, visual impairment, history of head trauma in the past six months. General hypermobility syndrome by Beaton's criteria and obtaining a score of five and above The difference in the length of the lower limbs Any disease that causes impaired motor or cognitive performance

Design outcomes

Primary

MeasureTime frame
Lower extremity reaction time. Timepoint: Before and immediately after treatment. Method of measurement: The reaction time of the knee is measured with the help of the reaction time measuring device, which is designed for this purpose. First, the designed software will be displayed on the monitor in front of the patient, and as soon as the desired image is seen on the monitor screen, the person will be asked to press the pedal placed under his foot once for the involved leg and once for the other leg. Non-involved press. These tests will be repeated 3 times for both legs. 5 to 7 minutes of rest will be included between each stage and the best score of the tests will be considered as the reaction time of the lower limbs of the participants.

Secondary

MeasureTime frame
Upper extremity reaction time. Timepoint: Before and immediately after treatment. Method of measurement: To measure reaction time in the upper limb, a computer program called DLRT software will be used. The working method will be that the participants will be asked to press a button on the keyboard as soon as they see a certain symbol on the monitor screen, so that the reaction time of their upper limbs is determined. Both upper limbs will do this. Each test was repeated 3 times. 5 to 7 minutes rest was included between each stage and the best score of the tests was considered as the reaction time of the participants.;Error ratio in the upper limb. Timepoint: Before and immediately after treatment. Method of measurement: The error rate (the number of wrong answers in image recognition) in the upper limb reaction time test, which will be implemented by the DLRT software, will be calculated by each person. Then the number of errors will be divided by the number of tests.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfsaneh Zeinalzadeh

Mashhad University of Medical Sciences

sps.Dean@mums.ac.ir+98 51 3884 6710

Outcome results

None listed

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