Influence of Acute Daily Workload Changes on Low-frequency Fatigue Morning Scores
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Screening Platform.
- Who it may be relevant to
- Registry conditions: Fatigue Intensity. Basic parameters: 16 years — 21 years · Male.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Influence of Acute Daily Workload Changes on Low-frequency Fatigue Morning Scores Throughout an In-season Soccer Microcycle
Overview
In recent years, the increased demands of both training and competition have heightened the need of load monitoring among soccer players. However, adopting metrics that comprehensively capture the intricacies of neuromuscular fatigue remains a challenge. Assessing low-frequency fatigue may contribute to fill this gap, as it provides an objective measure to evaluate muscle function readiness. Thus, the aim of this study was to examine whether variability in low-frequency fatigue morning scores are related to training external load acute changes throughout the in-season microcycle.
Interventions
- Diagnostic test Screening Platform
assessment of low-frequency fatigue using myocene
Primary outcome measures
- low-frequency fatigue [Time frame: Day 1 (0 hours), Day 2 (24 hours), Day 3 (48 hours), Day 4 (72 hours), Day 5 (96 hours), Day 6 (120 hours)]
Eligibility criteria
Inclusion criteria
- elite soccer players
Exclusion criteria
- injured athletes
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Case-control
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06704854 · ST_Myo_weekly