- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05981027
Static Stretching Exercises and Ultrasound Elastography Evaluation
March 20, 2024 updated by: Tahir Keskin , Pt, MSc, Suleyman Demirel University
Acute Effects of Static Stretching Exercises and the Mulligan Bent Leg Raise Technique on Hamstring Muscle Stiffness: an Ultrasound Elastography Evaluation
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.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Merkez
-
Isparta, Merkez, Turkey, 32200
- Süleyman Demirel Üniversitesi
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mulligan bent leg raise technique
A single session of 3 repetitions of Mulligan bent leg raise was applied to the participants.
|
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.
|
|
Experimental: Static stretching exercise
A single session of 5 repetitive stretching exercises was performed on the participants.
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Back-saver sit-and-reach test
Time Frame: Up to 2 months
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Two-dimensional Shear Wave Elastography
Time Frame: Up to 2 months
|
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
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 5, 2023
Primary Completion (Actual)
April 10, 2023
Study Completion (Actual)
February 28, 2024
Study Registration Dates
First Submitted
July 20, 2023
First Submitted That Met QC Criteria
July 31, 2023
First Posted (Actual)
August 8, 2023
Study Record Updates
Last Update Posted (Actual)
March 21, 2024
Last Update Submitted That Met QC Criteria
March 20, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- SuleymanDUtahirkeskin03
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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