NCT07861269

Not Yet Recruiting

Characterization of Hamstring and Quadriceps Neuromuscular F...

University Hospital, Strasbourg, France Source

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Other study identifiers

Sponsor study identifier

RC26_0128

Study Type

interventional

Estimated enrollment

20

Locations

0 countries

Sites

N/A

Timeline

Study Start

November 1, 2026

Estimated

Planned date reported by the registry; this milestone is not confirmed as achieved.

Primary Completion

June 2028

Estimated

Planned date reported by the registry; this milestone is not confirmed as achieved.

Study Completion

July 2028

Estimated

Planned date reported by the registry; this milestone is not confirmed as achieved.

Brief Summary

This is a monocentric study assessing hamstring and quadriceps neuromuscular fatigue after 3 consecutive soccer trainings. The purpose of this study was:

1.To quantify the difference of isometric force immediately after a simulated soccer training.
2.To characterize peripheral and central fatigue between hamstring and quadriceps muscles.
3.To compare the level neuromuscular fatigue before each session, to assess the cumulative effect of neuromuscular fatigue
4.To highlight correlation between neuromuscular fatigue and performance markers.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: not yet recruiting
Estimated enrollment: 20 participants
Study completion date: July 2028
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.
Listed locations: 0 countries · 0 sites

Trial Relationships

Click on a node to explore related trials.

Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
September 30, 2026
Actual (reported)
First Posted
October 6, 2026
Actual (reported)
Study Start
November 1, 2026
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.
Primary Completion
June 2028
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.
Study Completion
July 2028
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.

Last Updated: October 6, 2026
Status Verified: September 2026
Last Update Submitted: September 30, 2026

Conditions

Muscle Fatigue

Outcome Measures

Primary Outcomes (1)

Pre- to Post-Exercise Change in Maximal Isometric Knee Flexor and Extensor Strength
Before and immediately post exercise (i.e., during the first minute after cessation of exercise).

Study Arms (1)

Physical exercices arm

EXPERIMENTAL

Other: a simulated soccer training

Interventions

a simulated soccer trainingOther

contractions and electric impulses

Physical exercices arm

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age16 Years - 30 Years

Sexmale

Healthy VolunteersNo

Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

to be a soccer player, licensed to the French Football Federation
affiliation to the social health insurance scheme

You may not qualify if:

Sponsors & Collaborators

University Hospital, Strasbourg, France
Otherlead

Study Design

Study Type: interventional
Phase: not applicable
Allocation: NA
Masking: NONE
Purpose: BASIC SCIENCE
Intervention Model: SINGLE GROUP
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

September 30, 2026

First Posted

October 6, 2026

Study Start

November 1, 2026

Estimated

Planned date reported by the registry; this milestone is not confirmed as achieved.

Primary Completion

June 2028

Estimated

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Not ApplicableUnknown

NCT03460639

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Not ApplicableUnknown

impossibility to give the subject enlightened information (subject in emergency situation, difficulties in understanding the study, …)
subject under the protection of justice
subject under guardianship or curatorship
lower limbs musculotendinous or articular problems
smoker or having been a smoker in the last 5 years
subject wearing a pacemaker
drug treatment in progress and impossibility to stop it within 7 days before the beginning of the study.

Contact the study team to confirm eligibility.

Planned date reported by the registry; this milestone is not confirmed as achieved.

Study Completion

July 2028

Estimated

Planned date reported by the registry; this milestone is not confirmed as achieved.

Last Updated

October 6, 2026

Record last verified: 2026-09

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

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Registry identifier: NCT07861269
Data provider: ClinicalTrials.gov
Source updated: 2026-10-06
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:19:37 UTC

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Study Arms (1)

Physical exercices arm

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Design

Study Record Dates

Source record