The Most Demanding Match Periods: Should GPS Data be Normalized

December 20, 2025 updated by: Filipe Silvano Pinto Maia, University of Maia

The Most Demanding Match Periods: Should GPS Data be Normalized for Performance and Fatigue Monitoring in Soccer?

To date, the characterization of Most Demanding Periods (MDPs) in soccer has relied almost exclusively on absolute metrics, suggesting that the peak demands currently reported in the scientific literature are inherently shaped by these fixed thresholds. This reliance on such absolute metrics may lead to an under- or overestimation of the true relative intensity experienced by each player, thus limiting the accuracy of MDPs interpretation. Therefore, exploring whether normalized thresholds alter the magnitude of MDPs across a range of time windows (1, 3 and 5 minutes) is crucial to better understand how the most demanding passages of match play manifest when player-specific capacities are considered. Consequently, the aim of the present study was to compare the MDPs derived from absolute and normalized thresholds for HSR and sprinting.

Study Overview

Status

Active, not recruiting

Study Type

Observational

Enrollment (Estimated)

50

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

      • Maia, Portugal
        • Universidade da Maia

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

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Male Soccer players competing at the highest national level, free from injuries during the period of data analysis.

Description

Inclusion Criteria:

  • Soccer players competing at the highest national level

Exclusion Criteria:

  • Injured athletes

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Soccer Players
Soccer players enrolled in the research project
The most demanding periods will be compared over 3 different time windows: 1, 3 and 5 minutes. Both High speed running and sprint distances will be observed.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Distance covered
Time Frame: 1 minute, 3 minute, 5 minute
1 minute, 3 minute, 5 minute

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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, 2025

Primary Completion (Estimated)

December 30, 2025

Study Completion (Estimated)

January 30, 2026

Study Registration Dates

First Submitted

December 20, 2025

First Submitted That Met QC Criteria

December 20, 2025

First Posted (Actual)

January 7, 2026

Study Record Updates

Last Update Posted (Actual)

January 7, 2026

Last Update Submitted That Met QC Criteria

December 20, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • MDP_01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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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