The Effect of Lumbar and Sacroiliac Manipulation on Football Players (ELSMFP)

August 21, 2024 updated by: SEFA HAKTAN HATIK

Comparision of Instant Effect of Lumbal and Sacroiliac Spinal Manipulation on Flexibility and Jumping Performance in Licensed Football Players

The purpose of this study was to assess the immediate effects of chiropractic spinal manipulation methods on the lumbar and sacroiliac regions on professional soccer players' flexibility and leaping abilities.

Study Overview

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

Interventional

Enrollment (Actual)

45

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

      • Sinop, Turkey
        • Sefa Haktan Haktik

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

No

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

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: 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.
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
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.
This test was performed 5 minutes before and immediately after the manipulation.
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.
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.
This test was performed 5 minutes before and immediately after the manipulation.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: SEFA HAKTAN HATIK, Sinop University

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)

May 1, 2024

Primary Completion (Actual)

June 1, 2024

Study Completion (Actual)

August 1, 2024

Study Registration Dates

First Submitted

August 21, 2024

First Submitted That Met QC Criteria

August 21, 2024

First Posted (Actual)

August 23, 2024

Study Record Updates

Last Update Posted (Actual)

August 23, 2024

Last Update Submitted That Met QC Criteria

August 21, 2024

Last Verified

August 1, 2024

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

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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