- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06890845
Body Posture, Joint Mobility, and Trunk Muscle Endurance Related to Lower Back Pain in Tennis Players
Body Posture, Joint Range of Motion and Trunk Muscle Endurance in Relation to Low Back Pain in Tennis Players
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Warsaw, Poland, 01-126
- Mirai Clinic
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- provided written consent to participate in the study
For Study Group:
- playing tennis at least 3 times per week for the past 2 years
- experiencing back pain in the last 6 months that prevented playing tennis
For Comprarison Group I:
- playing tennis at least 3 times per week for the past 2 years
- no lower back pain (confirmed via survey) in the last 6 months that would have prevented playing tennis
For Comparison Group II:
- no lower back pain (confirmed via survey)
- regular physical activity at least 3 times a week
- no participation in asymmetrical sports
Exclusion Criteria:
- lack of written consent to participate in the study,
- history of surgical procedures involving the spine or torso,
- severe musculoskeletal pathologies in the medical history, such as previous cancers in the torso area, vertebral fractures, structural scoliosis,
- inability to assume the required test positions.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Study Group (SG)
Women and men amateur tennis players with LBP
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Comparison Group I (CGI)
Women and men amateur tennis players without LBP
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Comparison Group II (CGII)
Physically active women and men not engaged in asymmetric sports without LBP
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Hip range of motion
Time Frame: Baseline
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The hip range of motion was measured using a digital inclinometer. During hip rotation measurement, the subject lay prone with the pelvis stabilized by a strap. The tested hip was in a neutral position with the knee flexed to 90 degrees. The inclinometer was zeroed along the tibial axis when the tibial plateau was parallel to the ground. The range of motion was the angular difference between the initial and final positions. For flexion, the subject lay supine with the non-tested lower limb stabilized. The inclinometer was zeroed parallel to the ground. The final position was where the thigh could no longer move further into flexion. For extension, the subject .lay supine with the pelvis at the edge of the table. The subject maximally flexed both hips. The subject held the non-tested lower limb with both hands. On the tested side, the lower limb hung freely off the table. The inclinometer was zeroed on a surface parallel to the ground, and in the final position of the test. |
Baseline
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Spine range of motion
Time Frame: Baseline
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The measurement was conducted using a Baseline bubble inclinometer. For flexion, the patient stood in a relaxed position. The spinous processes of Th12 and S1 were palpated and marked. The inclinometer was zeroed at Th12, and the patient executed a full forward bend. The same was repeated at S1. The lumbar flexion range was the difference between readings at Th12 and S1. For extension, the patient also stood relaxed. Before measuring, the patient performed three maximum lumbar extensions. The inclinometer was zeroed at Th12, and the patient executed a maximum extension. The same procedure was repeated at S1. The lumbar extension range was the difference between readings at Th12 and S1. For lateral trunk flexion, the measurement was the distance between a point on the lateral thigh, where the tip of the third finger reached in a relaxed standing position, and a point on the thigh/shin after performing maximum lateral flexion. |
Baseline
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Modified sit and reach test
Time Frame: Baseline
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To perform the test, the subject sat on the examination table in such a way that one lower limb rested on the floor with the knee flexed at 90 degrees, while the other limb was placed on the table with the knee joint extended.
The subject positioned their hands in front of them, thumbs joined and palms facing down.
With elbows fully extended, the subject reached as far forward as possible, placing their hands on the table.
The distance from the tip of the third finger to the heel line was measured.
Positive results indicated that the tip of the third finger extended beyond the heel line, while negative results indicated that it was positioned before the heel line.
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Baseline
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Body posture
Time Frame: Baseline
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Posture assessment was conducted using the Diers Formetric 4D system, a non-invasive method with proven accuracy and reproducibility. This system employs surface topography for three-dimensional mapping of the subject's torso. The measurement followed the manufacturer's methodology. The subject stood 2 meters from the projector and camera, with foot placement marked on the treadmill. The back and neck were exposed, and undergarments adjusted to reveal the upper gluteal cleft. The subject assumed a relaxed standing position without posture correction. The examiner adjusted the projector height so that the central reference stripe aligned with the lower angle of the scapula. The device performed 12 scans in 6 seconds (2 Hz). The Diers software analyzed approximately 50,000 points on the subject's back, presenting a three-dimensional model of the spine with posture parameters. |
Baseline
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Trunk muscle endurance
Time Frame: Baseline
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The protocol for assessing trunk muscle endurance was based on the McGill et al. (1999) method.
[McGill, S. M., Childs, A., & Liebenson, C. (1999).
Endurance times for low back stabilization exercises: Clinical targets for testing and training from a normal database.
Archives of Physical Medicine and Rehabilitation, 80(8), 941-944.
https://doi.org/10.1016/s0003-9993(99)90087-4]
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Baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Oswestry Disability Index
Time Frame: Baseline
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The survey assessed the level of pain and disability associated with LBP.
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Baseline
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Custom survey for individuals not playing tennis
Time Frame: Baseline
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The survey covered spinal pain, health status, physical activity, and the presence of chronic diseases
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Baseline
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Custom survey for tennis players
Time Frame: Baseline
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The survey covered training volume, engagement in general conditioning and stretching exercises, presence of chronic diseases, history of injuries, and the level of spinal pain
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Baseline
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Collaborators and Investigators
Publications and helpful links
General Publications
- Chun SW, Lim CY, Kim K, Hwang J, Chung SG. The relationships between low back pain and lumbar lordosis: a systematic review and meta-analysis. Spine J. 2017 Aug;17(8):1180-1191. doi: 10.1016/j.spinee.2017.04.034. Epub 2017 May 2.
- Avman MA, Osmotherly PG, Snodgrass S, Rivett DA. Is there an association between hip range of motion and nonspecific low back pain? A systematic review. Musculoskelet Sci Pract. 2019 Jul;42:38-51. doi: 10.1016/j.msksp.2019.03.002. Epub 2019 Mar 30.
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- Research#Group no 4
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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