- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06555185
Acute Responses to a Potentiation Warm-up Protocol in Female Football Players.
August 12, 2024 updated by: University of Tromso
Acute Responses to a Potentiation Warm-up Protocol on Sprint and Change of Direction in Female Football Players: a Randomized Controlled Study
This study aims to determine if the performance of female football players is affected after exposure to a potentiation protocol.
It is hypothesized that performance in the selected physical tests will improve significantly and meaningfully after performing the chosen potentiation protocol compared to the control group's warm-up.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
17
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 Locations
-
-
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Famalicao, Portugal
- Futebol Clube de Famalicão
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- players from any playing position (except goalkeepers) able to train without limitations.
Exclusion Criteria:
- players with any existing medical conditions that could compromise participation.
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: Experimental group
Potentiation warm-up protocol with jumps combined with sprints with change of direction.
|
The intervention protocol consisted of i) 1st set - six hurdle jumps, with a distance of 70 cm between each, followed by a 15-m sprint with COD; (ii) 2nd set - six lateral hurdle jumps (three to the left and three to the right) followed by a 10-m sprint with COD; (iii) 3rd set - six bouncy strides, followed by a 15-m sprint with COD; (iv) 4th set - six broad jumps followed by a 10-m sprint with COD.
All COD circuits had different configurations, changing the sprint distance and the angle of the COD curve.
All repetitions and sets were separated by 90-second recovery intervals, and each set was performed three times.
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|
Active Comparator: Control group
Usual warm-up exercises as previously used by the whole team.
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The usual warm-up consisted of (i) The first phase included dynamic stretching and drills to increase body temperature.
This phase lasted 5-min and included slow jogging, light skipping, and dynamic stretches for hip flexors, glutes, quads, hamstrings, abductors, gastrocnemius and lower limb joints.
(ii) The second phase was composed of exercises that intended to mimic specific movements of the football match, both with and without ball possession.
This phase lasted 15 minutes and included exercises with and without possession of the ball, such as acceleration, COD, jumping over hurdles, and playful games with ball possession.
In this group, the players only rested in a slow jog when they moved from the first to the second phase.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Agility T-test
Time Frame: First moment: beginning of the first training session; Second moment: at the end of the third week, after the fourth protocol session had been completed.
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Used to determine speed with directional changes such as forward sprinting, left and right side shuffling.
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First moment: beginning of the first training session; Second moment: at the end of the third week, after the fourth protocol session had been completed.
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40-m sprint test
Time Frame: First moment: beginning of the first training session; Second moment: at the end of the third week, after the fourth protocol session had been completed.
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After a 5 s countdown, the participants ran forward following the route marked by cones, one at 0m indicating the start place and the other at 40m indicating the finish place.
Participants started the test from a standing start position with the front foot approximately 2 cm behind the first cone.
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First moment: beginning of the first training session; Second moment: at the end of the third week, after the fourth protocol session had been completed.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: Ivan Baptista, PhD, Faculty of Science and Technology, UiT The Arctic University of Norway
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)
April 30, 2023
Study Completion (Actual)
April 30, 2023
Study Registration Dates
First Submitted
August 12, 2024
First Submitted That Met QC Criteria
August 12, 2024
First Posted (Actual)
August 15, 2024
Study Record Updates
Last Update Posted (Actual)
August 15, 2024
Last Update Submitted That Met QC Criteria
August 12, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2022/03
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Raw data used for the study will be available in a public repository.
IPD Sharing Time Frame
Raw data is already uploaded into a public repository and is intended to stay available without a date limit.
IPD Sharing Access Criteria
No access criteria will be established.
Study Data/Documents
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Individual Participant Data Set
Information identifier: 10.17632/2cwcz2vx4v.1
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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