Examining Factors Influencing Thoracolumbar Mobility in Runners

February 20, 2024 updated by: Kübra Sarıoğlu, Hacettepe University

Examining Factors Influencing Thoracolumbar Mobility in Amateur Runners and Sedentary Individuals

The presence of to is thoracolumbar (TL) mobility a significant aspect in the context of running. Most of the factors may be related to certain kinematic parameters of the lumbopelvic-hip complex during running.

Study Overview

Detailed Description

Context: The presence of to is thoracolumbar (TL) mobility a significant aspect in the context of running. Most of the factors may be related to certain kinematic parameters of the lumbopelvic-hip complex during running. Objective: To compare the TL mobility of individuals at different running levels and sedentary individuals. Design: Cross-sectional. Participants: The first group consisted of 35 runners who had been running for the last two years (RTY) while the second group had 35 runners who had been running for the last six months (RSM). The third group had 35 sedentary individuals. Main Outcomes Measures: Sports-related and sociodemographic information was recorded. The Myoton device was used over the Latissimus Dorsi (LD) muscle on both dominant and nondominant sides to measure muscle tone (Hz), elasticity, and stiffness (N/m) values. Trunk flexibility and flexibility of lumbar extensor muscles were measured with tape measurement (cm). The trunk range of motion (ROM, ˚) was measured using goniometer. Thoracolumbar Fascia Length Test and Modified Schober Test were used for thoracolumbar (TLF) fascia flexibility. Analysis of variance was used for statistical analysis. SPSS version 17.0 was used for all statistical analyses. The primary outcome was defined as lumbar extensor tightness. Numeric data obtained from the subjects were presented as mean, standard deviation (mean±SD) and percentage (%). The primary outcome was defined as lumbar extensor tightness. The sample size for each group was calculated to be 30 with a power of 80% and a significance level of 0.05. Considering potential dropouts, 35 participants were included in each group. The groups were not homogenous. As a nonparametric test, the 'Kruskal-Wallis test' was employed for the three-group comparison. The Mann-Whitney U test was used for the two-group comparison. Statistical significance was set at P < .05.

Study Type

Observational

Enrollment (Actual)

90

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

    • Altındağ
      • Ankara, Altındağ, Turkey, 06100
        • Hacettepe University

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

Sampling Method

Probability Sample

Study Population

The participants were recreational runners who run between 20 to 50 km weekly. The first group consisted of 35 runners who had been running for the last two years (RTY) while the second group had 35 runners who had been running for the last six months (RSM).

The third group was composed of 35 sedentary individuals identified using the Sedentary Behavior Questionnaire.

Description

Inclusion Criteria:

  • The participants were within the age range of 30 to 45.

Exclusion Criteria:

  • The history of lower extremity or lumbar-related surgery within the last year and a body mass index (BMI) exceeding the normal threshold of 24.5 kg/m².

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
There are 3 groups. 2 groups consist of runners and 1 group consists of sedentary individuals.
Participants were recreational runners who run between 20 to 50 km weekly; one group consisted of 35 runners who had been RTY, the second group consisted of 35 runners who had been running for RSM; the third group was composed of 35 sedentary individuals identified using the Sedentary Behavior Questionnaire. Participants were within the age range of 30 to 45. Exclusion criteria encompassed a history of lower extremity or lumbar-related surgery within the last year and a body mass index (BMI) exceeding the normal threshold of 24.5 kg/m².
The Myoton device was used over the Latissimus Dorsi (LD) muscle on both dominant and nondominant sides to measure muscle tone (Hz), elasticity, and stiffness (N/m) values. Trunk flexibility and flexibility of lumbar extensor muscles were measured with tape measurement (cm). The trunk range of motion (ROM, ˚) was measured using goniometer. Thoracolumbar Fascia Length Test and Modified Schober Test were used for thoracolumbar (TLF) fascia flexibility. The weekly training distance (km), duration (h) and daily water consumption (lt) rates were recorded. The percentage of individuals experiencing lower extremity injuries and lower back pain within the RSM group was calculated.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Myoton Assessment
Time Frame: 1 month
The passive mechanical properties of the muscle (Tone, Stiffness, and Elasticity) were measured using the Myoton-3 myotonometer medical device (Myoton Ltd., Estonia, EU) (ICC: 0.80-0.93). The patients were positioned prone with a thin rolled towel placed under their foreheads and their arms in a 180˚ flexion position for a fifteen-minute period of rest. In our study, a point 5 cm below the lower tip of the scapula was identified along the imaginary line of the LD muscle. The probe was at a 90˚ angle to the skin. The measurements were repeated ten times at one-second intervals and the average values were recorded. These values were then calculated for dominant and nondominant sides.
1 month

Collaborators and Investigators

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

Investigators

  • Study Director: Hacettepe University, 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)

September 1, 2022

Primary Completion (Actual)

January 1, 2023

Study Completion (Actual)

January 1, 2024

Study Registration Dates

First Submitted

February 11, 2024

First Submitted That Met QC Criteria

February 19, 2024

First Posted (Actual)

February 21, 2024

Study Record Updates

Last Update Posted (Actual)

February 22, 2024

Last Update Submitted That Met QC Criteria

February 20, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • HU-FTR-KS-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

I don't study for a doctorate. I want the data to remain private. But I will share my results. I think it will be enough to give my opinion in the discussion part.

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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