- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04713696
Core Stability for Baseball Batting in Adolescents
January 14, 2021 updated by: Yi Liang Kuo, National Cheng-Kung University Hospital
Using Functional Movement Patterns to Investigate the Impact of Core Stability on Hitting Mechanics and Bat Swing Velocity in High School Baseball Players
Baseball batting is important to winning the games.
Baseball batting is achieved by proximal-to-distal sequencing of body movements and controlled by the neuromuscular system.
Poor lumbopelvic control could influence production and transfer of energy in the kinetic chain.
This study aims to investigate the effects of functional movement training on hitting mechanics and bat swing velocity in high school baseball players.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
60
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 Contact
- Name: Yi-Liang Kuo, PT, PhD
- Phone Number: 6251 +88662353535
- Email: yiliangkuo@mail.ncku.edu.tw
Study Locations
-
-
-
Tainan, Taiwan, 701
- Recruiting
- National Cheng Kung University
-
Contact:
- He-Xin Cheng, PT, BS
- Phone Number: 5930 +8862353535
- Email: tyagr14@gmail.com
-
-
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
12 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Sport specialization in baseball batting
- Active players on baseball teams
Exclusion Criteria:
- History of surgery in the lumbar area
- Severe musculoskeletal or neurological symptoms that interfere with participation in competition, training or tests
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Functional training
Participants received functional training
|
Functional training refers to exercises that targets the muscles of the lumbopelvic-hip complex in order for them to more appropriately support and control the spine.
|
Active Comparator: Routine training
Participants received routine training
|
Routine training refers to general exercises that perform before and after practice, including jogging, stretching and strengthening exercises for upper and lower extremities
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Bat-swing velocity
Time Frame: Changes from baseline to 8 weeks post intervention
|
Maximal bat swing velocity during baseball batting measured by the VICON motion analysis system
|
Changes from baseline to 8 weeks post intervention
|
Batting movement
Time Frame: Changes from baseline to 8 weeks post intervention
|
Batting movement measured by the VICON motion analysis system
|
Changes from baseline to 8 weeks post intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dynamic balance
Time Frame: Changes from baseline to 8 weeks post intervention
|
Dynamic balance measured by the Y-balance Test (YBT)
|
Changes from baseline to 8 weeks post intervention
|
Functional performance
Time Frame: Changes from baseline to 8 weeks post intervention
|
Functional performance measured by Functional Movement Screen (FMS)
|
Changes from baseline to 8 weeks post intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Yi-Liang Kuo, PT, PhD, National Cheng Kung 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)
December 12, 2020
Primary Completion (Anticipated)
July 1, 2023
Study Completion (Anticipated)
December 1, 2023
Study Registration Dates
First Submitted
January 3, 2021
First Submitted That Met QC Criteria
January 14, 2021
First Posted (Actual)
January 19, 2021
Study Record Updates
Last Update Posted (Actual)
January 19, 2021
Last Update Submitted That Met QC Criteria
January 14, 2021
Last Verified
January 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- B-ER-108-072
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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