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Clinical Trials/NCT06555185
NCT06555185CompletedNot Applicable

Acute Responses to a Potentiation Warm-up Protocol on Sprint and Change of Direction in Female Football Players: a Randomized Controlled Study

University of Tromso2 sites in 1 country17 target enrollmentStarted: September 1, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
17
Locations
2
Primary Endpoint
Agility T-test

Study Overview

Brief Summary

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 Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Sex
Female
Accepts Healthy Volunteers
No

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.

Outcomes

Primary Outcomes

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.

Used to determine speed with directional changes such as forward sprinting, left and right side shuffling.

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.

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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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