- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06252740
Investigation of Regional Interdependence of the Hip and Spine in Baseball Players With Low Back Pain
February 1, 2024 updated by: National Cheng-Kung University Hospital
Low back pain (LBP) is a common musculoskeletal symptom in athletes.
More than 40% percent of high school baseball players reported incidents of LBP during the previous year.
University baseball athletes were 3.23 times more likely to have lumbar intervertebral disk degeneration than the nonathletic university students.
According to the regional interdependence model, a patient's chief complaints may be directly or indirectly related to or influenced by physical impairments from various body systems and regardless of proximity to the primary symptom(s).
Athletes with a chief complaint of LBP frequently demonstrate with mobility restrictions in the thoracic spine and hips, which may contribute to compensatory hypermobility in the lumbar spine and subsequently lead to LBP.
Few studies have examined the relationship between thoracic spine mobility and LBP, while many studies investigating the relationship between hip joint mobility and LBP in athletes showed inconsistent results.
The inconsistent results may be due to different types of sports and measurement methods.
Therefore, the objectives of this research project are to: (1) examine if baseball players with a history of LBP have mobility restriction in the thoracic spine and hips and movement coordination within the spine and hip regions during baseball batting that are different from those without a history of LBP; (2) identify thoracic spine and hip joint mobility and coordination related predictors for batting velocity and LBP in baseball players.
This 2-year research project plans to recruitment a total of 110 male baseball players aged between 18 and 30 years from university and community recreational league baseball teams (55 players with a history of LBP and 55 age-matched players without a history of LBP).
Participants will receive physical examination for the thoracic spine and hip joints (joint mobility and muscle stiffness) and 3D motion analysis for baseball batting.
The results of this research project will guide the development of more specific and effective treatment and preventative training for baseball players with LBP and enhance their batting performance.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
40
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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Tainan, Taiwan, 701
- National Cheng Kung University
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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
Yes
Sampling Method
Non-Probability Sample
Study Population
university and recreational leagues baseball teams
Description
Inclusion Criteria:
• Baseball players who had experienced at least 2 episodes of LBP that limits their performance for a period of greater than 3 days in the previous year.
Exclusion Criteria:
- Current LBP symptoms including weakness and numbness in the lower extremities
- Previous surgery to the back, upper or lower extremities
- Marked spinal deformity (e.g., scoliosis, or kyphosis)
- Any other orthopedic or medical problem that would have limited their ability to fully participate in baseball training and competition in the last year.
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 |
|---|---|
|
control group
Baseball players without a history of low back pain
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Comare the difference in batting mechanics, hip and thoracic spine mobility, and muscle stiffness in baseball players with and without a history of low back pain
|
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experimental group
Baseball players with a history of low back pain
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Comare the difference in batting mechanics, hip and thoracic spine mobility, and muscle stiffness in baseball players with and without a history of low back pain
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Angular displacement of spine during baseball batting
Time Frame: immediately after enrollment
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Measured by the Vicon motion analysis system in the horizontal plane
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immediately after enrollment
|
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Angular displacement of hip during baseball batting
Time Frame: immediately after enrollment
|
Measured by the Vicon motion analysis system in the horizontal plane
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immediately after enrollment
|
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Angular velocity of spine during baseball batting
Time Frame: immediately after enrollment
|
Measured by the Vicon motion analysis system in the horizontal plane
|
immediately after enrollment
|
|
Angular velocity of hip during baseball batting
Time Frame: immediately after enrollment
|
Measured by the Vicon motion analysis system in the horizontal plane
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immediately after enrollment
|
|
Thoracic spine mobility
Time Frame: immediately after enrollment
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Measured by the Vicon motion analysis system in sitting
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immediately after enrollment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hip joint mobility
Time Frame: immediately after enrollment
|
Ranges of hip internal and external rotation measured by inclinometer in sitting
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immediately after enrollment
|
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Stiffness of biceps femoris muscle
Time Frame: immediately after enrollment
|
Measured by the hand-held MyotonPRO device in N/m
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immediately after enrollment
|
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Stiffness of rectus femoris muscle
Time Frame: immediately after enrollment
|
Measured by the hand-held MyotonPRO device in N/m
|
immediately after enrollment
|
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Stiffness of tensor fasciae latae muscle
Time Frame: immediately after enrollment
|
Measured by the hand-held MyotonPRO device in N/m
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immediately after enrollment
|
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Stiffness of glutues maximus muscle
Time Frame: immediately after enrollment
|
Measured by the hand-held MyotonPRO device in N/m
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immediately after enrollment
|
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Stiffness of thoracic erector spinae muscle
Time Frame: immediately after enrollment
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Measured by the hand-held MyotonPRO device in N/m
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immediately after enrollment
|
|
FABER's test
Time Frame: immediately after enrollment
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Measured as distance between knee and bed in cm
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immediately after enrollment
|
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Straight leg raising test
Time Frame: immediately after enrollment
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Measured as hip flexion angle (with knee extended) in degree
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immediately after enrollment
|
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Modified Thomas test
Time Frame: immediately after enrollment
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Measured as hip flexion angle (with knee flexed) in degree
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immediately after enrollment
|
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Ober test
Time Frame: immediately after enrollment
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Measured as hip adduction angle in degree
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immediately after enrollment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
November 2, 2022
Primary Completion (Estimated)
July 31, 2024
Study Completion (Estimated)
July 31, 2024
Study Registration Dates
First Submitted
May 16, 2023
First Submitted That Met QC Criteria
February 1, 2024
First Posted (Actual)
February 12, 2024
Study Record Updates
Last Update Posted (Actual)
February 12, 2024
Last Update Submitted That Met QC Criteria
February 1, 2024
Last Verified
November 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- A-ER-110-579
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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