ClinicalTrials.gg
RecruitingNCT06458166Updated Jun 13, 2024

Associations Between Low Frequency Fatigue, Jump Height and Perceptual Measures of Muscle Soreness, Fatigue and Recovery

An observational study in Fatigue and Physical Exercise, sponsored by University of Maia. Recruiting at 1 site in Portugal. Open to male participants aged 16 Years to 21 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-13.

Sponsored by University of Maia · Observational

From the registry’s dates

  • Primary completion was expected by Aug 2024, 2 years 2 months ago, but the record still lists the study as recruiting.
Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
40
Ages
16 Years to 21 Years
Sex
Male
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 11 studies in Fatigue with a site in Portugal — 3 open to participants now, 4 under way, 1 of them phase 3. Fatigue · Portugal.

Started
2024
with 2 others
Observational
5 of 11
2 open now
Registered
7th of 11
by date
Lead sponsor
1 of 11
University of Maia

Among the 11 studies in Fatigue with a site in Portugal, this one is one of 3 that started in 2024, is one of 5 observational ones, and was the 7th registered.

Fatigue

2,229 studies on the registry are indexed under Fatigue; 426 are open to participants now.

Browse Fatigue studies →

Open to participants now

3 of the 11 studies in Fatigue with a site in Portugal are open now. Recruiting first, the newest first:

All 3 open studies →

A study can be open while its sites in Portugal have not opened yet or have stopped. Only those recruiting at a site in Portugal →

Who these studies take

Of the 240 Fatigue studies recruiting now, 112 (47%) set no upper age limit and 98 (41%) stop at 75 or younger; 24 take children under 18; 74 take healthy volunteers.

This study: 16 Years to 21 Years · male · healthy volunteers too.

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02

Study summary

Over the recent years, the increased competitive demands in elite competitive athletes has sparked a heightened interest in monitoring fatigue. Given the nature of the soccer game, athletes may experience low-frequency fatigue. Until recently, this assessment was restricted to in-lab. However, the emergence of new instruments aiming to allow low-frequency assessment to be carried out on a daily basis, in the context of professional teams. This study aimed to analyze the recovery of low-frequency fatigue, jump height and perceptual responses following competition and investigate possible associations between the objective and subjective parameters.

03

Conditions studied

  • Fatigue
  • Physical Exercise

Keywords

  • sports
  • soccer
  • low frequency fatigue
04

Who can participate

Ages eligible
16 Years to 21 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Players at the highest division of the portuguese national championships in their respective age group.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Elite level youth soccer players, competing in the highest portuguese division

Exclusion criteria

Exclusion Criteria:

  • Older adults
  • none elite soccer player
  • Play less than 70 minutes of match
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
40 participants (estimated)
Patient registry
No

Interventions

  • OtherAssessment of low frequency fatigue using low frequency eletrical stimulation

    Pre-programmed muscle electrical stimuli will be applied via Myocene® software using 3 electrodes: 1 cathode (5 x 10 cm) placed transversely over the proximal quadriceps femoris, and 2 anodes (5 x 5 cm) over the distal vastus medialis and vastus lateralis. Sixteen sets of stimuli will be administered with 5 seconds between sets. Each set consists of a single pulse, a train of 5 stimuli at 20 Hz, and a train of 18 stimuli at 120 Hz, with 1-second intervals between. The stimulation intensity starts at 25 mA and increases by 1 mA per set, reaching 40 mA in the final set. The Myocene® software calculates the ratio of low- to high-frequency evoked forces within each set. The outcome (Powerdex) is the median value of these 16 ratios for each leg. This evaluation will be conducted on both legs, taking 2 minutes per leg.

06

What researchers measure

Primary outcomes

  1. Differences in Low frequency fatigue measured using Myocene (eletrical stimulus and force measurement)

    Assessment using myocene. Muscles are stimulated with low-frequency electrical pulses. The response of the muscle (force or torque) output, is recorded. A decrease in force output compared to baseline levels indicates fatigue.

    Time frame: 2 hours before the match; 30 minutes following the match, 24 hours following the match; 48 hours following the match

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jul 2024; primary completion for Aug 2024, 1 month later.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 1, 2024
First posted
Jun 13, 2024
StartEst.
Jul 1, 2024
Primary completionEst.
Aug 21, 2024
CompletionEst.
Sep 30, 2024
Last update
Jun 13, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 13, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06458166
Lead sponsor
University of Maia
Responsible party
Filipe Silvano Pinto Maia (Principal Investigator, University of Maia) — Principal investigator
First posted
Jun 13, 2024
Start date
Jul 1, 2024 (estimated)
Primary completion
Aug 21, 2024 (estimated)
Completion
Sep 30, 2024 (estimated)
Last update
Jun 13, 2024

Study contacts

Filipe Maia
Contact
FMAIA.dcd@umaia.pt
22 986 6000

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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