- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05691673
Upper Extremity Force-velocity Profile in Swimmers
January 10, 2023 updated by: Ferhat Öztürk, Hacettepe University
The Effect of Training Periodization on the Upper Extremity Force-velocity Profile in Swimmers During a Macro Cycle
The aim of this study was to measure the changes in the upper extremity force-velocity profile of young swimmers at different training periods during a training season
Study Overview
Detailed Description
Tested at each experimental test time point (Baseline: E1, post-general preparation: E2, post-specific E3 and post-competition season: E4).
To measure the upper extremity force-velocity parameters, the countermovement push-up test was performed using the force plate
Study Type
Observational
Enrollment (Actual)
20
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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Ankara, Turkey, 06100
- Hacettepe 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
15 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Health young swimmers in competitive club
Description
Inclusion Criteria:
- 15-18 age
- go to training regularly
Exclusion Criteria:
- upper extremity surgery in the last 1 year
- pain during the 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
- Observational Models: Case-Control
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The change in the parameters of the force (Newton) obtained from the force platform with countermovement push up from the baseline to the end of the season.
Time Frame: Baseline: E1, (week 0) post-general preparation: E2 (week 6), post-specific E3 ( week12) and post-competition season: E4 (week 16).
|
Tested at each experimental test time point (Baseline: E1, post-general preparation: E2, post-specific E3 and post-competition season: E4).
To measure the upper extremity force-velocity parameters, the countermovement push-up test was performed using the force plate.
|
Baseline: E1, (week 0) post-general preparation: E2 (week 6), post-specific E3 ( week12) and post-competition season: E4 (week 16).
|
|
velocity (m/s)
Time Frame: Baseline: E1, (week 0) post-general preparation: E2 (week 6), post-specific E3 ( week12) and post-competition season: E4 (week 16).
|
Tested at each experimental test time point (Baseline: E1, post-general preparation: E2, post-specific E3 and post-competition season: E4).
To measure the upper extremity force-velocity parameters, the countermovement push-up test was performed using the force plate.
|
Baseline: E1, (week 0) post-general preparation: E2 (week 6), post-specific E3 ( week12) and post-competition season: E4 (week 16).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 13, 2021
Primary Completion (Actual)
August 19, 2022
Study Completion (Actual)
October 15, 2022
Study Registration Dates
First Submitted
December 16, 2022
First Submitted That Met QC Criteria
January 10, 2023
First Posted (Actual)
January 20, 2023
Study Record Updates
Last Update Posted (Actual)
January 20, 2023
Last Update Submitted That Met QC Criteria
January 10, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GO 21/1151
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
IPD Plan Description
Undecided
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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