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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06009406
Other study ID # graston
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2023
Est. completion date June 1, 2023

Study information

Verified date March 2024
Source Mugla Sitki Koçman University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In our study, we aimed to compare the effects of both Graston technique and static stretching on ankle range of motion and vertical jump performance in the light of the literature. Our study will guide clinicians about the uncertainty in the application of Graston technique and static stretching to the gastrocnemius, soleus muscles and Achilles tendon and examine the applicability of Graston in athletes. It is also aimed to investigate the relationship between ankle range of motion and vertical jump performance.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 1, 2023
Est. primary completion date May 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - The participant has volunteered and agreed to participate with the consent form - The participant is between the ages of 18-40 - The participant is able to perform the squat movement pattern - Participant must be an active and licensed athlete Exclusion Criteria: - Health problem that will affect the participant's mobility or jump performance - The participant has had a surgical procedure involving the ankle and knee in the last 6 months - The presence of orthopedic injury of the participant's foot and ankle - Participant has a neurological diagnosis - The participant is pregnant - The participant has an acute lower extremity injury

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Physiotherapy
This group will be applied to the soleus, gastrocnemius muscle and Achilles tendon with Graston, an instrumental myofascial mobilization technique, until they feel warmth in the skin and tonus relaxation in the target muscles. The control group will be subjected to 3 repetitions of passive stretching for 30 seconds for the same structures.

Locations

Country Name City State
Turkey FizyoMove Istanbul Üsküdar

Sponsors (1)

Lead Sponsor Collaborator
Mugla Sitki Koçman University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Vertical Jump Test (VJT) It is a test with a high reliability rate for determining the athlete's jumping power. It was developed by Dr. Dudley Allen Sargent in 1921. In the test, a tape measure is attached to the wall. Stand upright with the feet shoulder-width apart and the dominant side facing the wall. Without lifting the feet off the floor, the highest point that can be reached on the tape measure is marked. Then, immediately after bending down by bending the hips and knees, the highest point that can be reached by jumping is asked to be marked by hand. The distance difference between both points is determined. The test is repeated three times and the best result is recorded in centimeters. Change from Baseline VJT at 10 minutes
Primary Universal Goniometric Measurement (UGM) The participant lies supine with the knee extended and the ankle hanging over the end of the table. Inversion, eversion, dorsi flexion and plantar flexion active ankle range of motion can be assessed using a goniometer. In the universal goniometric measurement, the 90-degree right angle between the 5th metatarsal and fibula is considered the starting position of the ankle at 0 degrees for dorsi and plantar flexion. Since the gastrocnemius covers two joints, the muscle should be relaxed by placing a thin pillow under the knees during the measurement. The pivot point of the goniometer is placed on the lateral malleolus. The fixed arm is held parallel to the lateral midline of the fibula. The movable arm follows the lateral midline of the 5th metatarsal bone. Care is taken to avoid inversion and eversion of the foot during measurement. Change from Baseline UGM at 10 minutes
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