- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06568666
The Effect of Lumbar and Sacroiliac Manipulation on Football Players (ELSMFP)
Comparision of Instant Effect of Lumbal and Sacroiliac Spinal Manipulation on Flexibility and Jumping Performance in Licensed Football Players
Study Overview
Status
Intervention / Treatment
Detailed Description
The study included 45 professional soccer players who were previously informed about the study and met the inclusion criteria. The 45 participants were then randomly divided into three groups: lumbar manipulation group (n=15), sacroiliac joint manipulation group (n=15) and control group (n=15).
The V-Sit Reach Test was used to assess flexibility, the vertical jump test (on the wall) was used to assess vertical jump, and horizontal jump was assessed with the help of a tape on the hall floor. Each test was repeated twice and the best result was recorded in centimeters (cm.). Five minutes after the initial tests were performed, the lumbar spinal manipulation group underwent lumbar spinal manipulation on the identified dysfunctional segment, the sacroiliac joint manipulation group underwent sacroiliac joint manipulation on the dysfunctional side, and the control group did not receive any treatment.
The same tests were then repeated without any waiting period and the best result was recorded.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Sinop, Turkey
- Sefa Haktan Haktik
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Signing the voluntary consent form
- Being a male
- Being between ages of 18 - 35
- Playing professional soccer for a minimum of 6 months
- Asymptomatic dysfunction of the lumbar spine or sacroiliac joint.
Exclusion Criteria:
- Having an injury in the lower extremities
- Lumbar spine and sacroiliac region in the last 6 months
- Having a contraendication to the chiropractic treatments
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Lumbar manipulation group
Lumbar spinal manipulation was also performed in the lateral recumbent position and HVLA thrust was applied to the segment where dysfunction was detected.
The spinal process was determined as the contact point and the direction of HVLA thrust was from posterior to anterior.
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Lumbar spinal manipulation was performed in the lateral recumbent position and HVLA thrust was applied to the segment where dysfunction was detected.
The spinal process was determined as the contact point and the direction of HVLA thrust was from posterior to anterior.
|
|
Experimental: Sacroiliac Joint Manipulation Group
The participant lies on his/her side on the healthy side; the lower knee is in extension while the upper knee is flexed and placed in the popliteal fossa of the lower knee.
The participant's hands are left free on the ribs at the lower level.
The practitioner crosses the movement barrier with the stabilizing hand, allowing the tissues to relax.
The practitioner performs HVLA thrust of the iliac bone into posterior or anterior rotation (in the opposite direction of dysfunction) with the stabilizing hand.
|
The participant lies on his/her side on the healthy side; the lower knee is in extension while the upper knee is flexed and placed in the popliteal fossa of the lower knee.
The participant's hands are left free on the ribs at the lower level.
The practitioner crosses the movement barrier with the stabilizing hand, allowing the tissues to relax.
The practitioner performs HVLA thrust of the iliac bone into posterior or anterior rotation (in the opposite direction of dysfunction) with the stabilizing hand
|
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No Intervention: Control Group
No treatment has been carried out.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
V-Sit Reach Test
Time Frame: This test was performed 5 minutes before and immediately after the manipulation.
|
The participant is advised to sit on the floor with his legs straight front.
The toes are pointed up, the heels are in touch with the ground, and there is about a 30-centimeter distance between them.
A line is drawn connecting the spots where the heels strike the ground, and this line is used as the zero line for measurements.
The patient is urged to reach forward with his hands as far as he can while keeping his knees extended.
The distance between the attained point and the zero point is measured in centimeters.
The numerical value is preceded by (+) and (-), which denote the location relative to the zero point.
The knees should be kept in extension during the test.
To obtain a measurement result, the tested person repeats the movement twice and the practitioner records the best result (+) or (-) in cm.
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This test was performed 5 minutes before and immediately after the manipulation.
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Vertical Jump
Time Frame: This test was performed 5 minutes before and immediately after the manipulation.
|
The athlete stands facing the platform allocated for the test.
With one arm, he/she reaches the highest point possible, and the test administrator marks the platform.
The athlete jumps and touches the highest place he or she is able to reach, and is then noted.
The test administrator measures the distance between these two spots and notes it in centimeters.
The test must be taken twice.
The best results are considered.
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This test was performed 5 minutes before and immediately after the manipulation.
|
|
Horizontal Jump
Time Frame: This test was performed 5 minutes before and immediately after the manipulation.
|
It is a test that assesses athletes' balance, jumping strength, and lower extremity strength in both vertical and horizontal planes.
The test starting location is marked on the floor with a marker.
In this stance, the individual being tested waits for the required acceleration.
They leap as far as possible utilizing their single and double legs, as directed by the test administrator.
The distance from the starting position to the leap point is measured.
The test is repeated twice, and the best result is recorded in centimeters.
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This test was performed 5 minutes before and immediately after the manipulation.
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: SEFA HAKTAN HATIK, Sinop University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- CMT003
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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