- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07321496
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
Conditions
Intervention / Treatment
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.
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 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
Keywords
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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