- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06269224
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
Status
Completed
Conditions
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
-
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Altındağ
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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.
Sponsor
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
Keywords
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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