Static Stretching Exercises and Ultrasound Elastography Evaluation

Elastography Clinical Trial

Official title:

Acute Effects of Static Stretching Exercises and the Mulligan Bent Leg Raise Technique on Hamstring Muscle Stiffness: an Ultrasound Elastography Evaluation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05981027
• Other study ID #: SuleymanDUtahirkeskin03
• Status: Completed
• Phase: N/A
• Start date: January 5, 2023
• Est. completion date: February 28, 2024

Study information

• Verified date: March 2024
• Source: Suleyman Demirel University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of thid study was to compare two methods applied to increase the flexibility of the hamstring muscles and objectively evaluate changes in muscle stiffness using the two-dimensional shear wave ultrasound elastography (2D SWE) method. Thirty asymptomatic young individuals with hamstring shortness were divided into two groups by simple randomization. The Mulligan bent leg raise (BLR) technique was applied to the first group, and passive static stretching exercises to the second group. Hamstring flexibility was evaluated with the sit-and-reach test, and muscle stiffness with the 2D SWE method.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: February 28, 2024
• Est. primary completion date: April 10, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 20 Years to 25 Years

Eligibility

Inclusion Criteria:

• Having a limitation of more than 25° in the active knee extension test
• Only engaged in recreational sports during the study period

Inclusion Criteria:

• Having a history of lower extremity injury within the last two years
• Not volunteering to participate in the study.

Related Conditions & MeSH terms

• Elastography
• Muscle Stretching Exercise

Intervention

Other:
• Mulligan bent leg raise technique
In this study, while the participant was lying on his back on a high bed, the physiotherapist sat on the lateral side of the leg to be treated, placing the popliteal fossa of the participant's knee on his shoulder. The hip and knee of the leg to be stretched were placed in 90° flexion. Distraction was applied to the lower end of the femur, and the participant was asked to push the physiotherapist's shoulder with his leg and then relax. At this relaxation point, the physiotherapist pushed the flexed knee as far as possible in the direction of the ipsilateral shoulder in a painless range.
• Static stretching exercise
The participant lay on a stretcher in the supine position with his back straight. The physiotherapist placed the participant's leg on his shoulder with the knee in full extension and supported by the ankle and flexed the hip as much as possible until a tension was felt in the posterior thigh. This position was maintained for 30 seconds.

Locations

Country	Name	City	State
Turkey	Süleyman Demirel Üniversitesi	Isparta	Merkez

Sponsors (1)

Lead Sponsor	Collaborator
Suleyman Demirel University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Back-saver sit-and-reach test	The difference between the back-saver sit-and-reach test and the classical sit-and-reach test is that the former is applied unilaterally. The test was administered using the sit-and-reach test box. The participants were asked to sit on a flat surface and rest the sole of one of their feet flat on the end of the box while keeping the other leg flat on the floor by flexing the knee and hips to 90° and 45° sequentially. Maintaining this position, they were asked to place one hand on the other with their palms facing down, slide their hands on the measuring board, slowly reach forward, wait for a second or two at the last point reached	Up to 2 months
Secondary	Two-dimensional Shear Wave Elastography	All 2D SWE examinations were performed by a specialist radiologist using the Philips EPIQ-7 (EPIQ Elite Diagnostic Ultrasound System Release 7.0.5 Philips) device with an 18-4 MHz linear probe. These measurements were made with the patient lying in the prone position, with the knees in full extension, the ankle at the end of the stretcher, and the feet hanging down. The probe was placed longitudinally in the middle 1/3 of the hamstring muscles. The participants were asked to keep their muscles in a relaxed position, and no extra pressure was applied to the probe to avoid tissue compression that could artificially affect the measured tissue stiffness	Up to 2 months