- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04695067
The Influence of Central and Peripheral Fatigue on Sports Performance and Prevention of Sports Injury
April 16, 2024 updated by: National Taiwan University Hospital
Cooperation Between NTU and NTUS: Integrated Precision Approach to Improve Baseball Skills, Tactics and Competition Performance-The Influence of Central and Peripheral Fatigue on Sports Performance and Prevention of Sports Injury
This is an observational study that assess the baseball pitchers' fatigue status.
The purpose of this study is to find the pitching mechanic change and the fatigue point to provide guidance for coaches to schedule training items .
It is expected that earlier detect the pitchers' fatigue point could be able to prevent overuse injury caused by compensatory actions.
Study Overview
Detailed Description
The expected outcomes of this study include providing more reliable scientific evidence of the effects of fatigue on baseball players' performance and movement control, which can help to improve muscle endurance and the quality of movement control.
Moreover, fatigue that resulted from the prolonged practice can be reduced and recovered faster after exercise, as well as more understanding on the ideal pitching posture and compensatory action that caused by fatigue, providing a guideline for exercise training.
This will not only help to prevent fatigue and reduce risk of injury, but also strengthen weak muscle groups and improve movement strategies before matches, as well as lengthen the time of being a baseball player.
Study Type
Observational
Enrollment (Actual)
29
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: Wei-Li Hsu, PhD
- Phone Number: +886-2-3366-8149
- Email: wlhsu@ntu.edu.tw
Study Locations
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-
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Taipei, Taiwan, 100
- Taiwan
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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
18 years to 35 years (Adult)
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
baseball pichers
Description
Inclusion Criteria:
- healthy baseball pitchers
- age between 18~35 years old
Exclusion Criteria:
- surgery history in pitching arm
- Musculoskeletal disease
- Neuromuscular disease
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
heart rate variability (HRV)
Time Frame: 8 weeks
|
test HRV during pitches
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Wei-Li Hsu, PhD, National Taiwan 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)
October 8, 2018
Primary Completion (Actual)
July 31, 2023
Study Completion (Actual)
July 31, 2023
Study Registration Dates
First Submitted
December 31, 2020
First Submitted That Met QC Criteria
January 4, 2021
First Posted (Actual)
January 5, 2021
Study Record Updates
Last Update Posted (Actual)
April 18, 2024
Last Update Submitted That Met QC Criteria
April 16, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201807126RINA
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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