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Athletic PerformanceUnlocking PAPENCT07511348

Neuromuscular Adaptations Following Eight Weeks of French Contrast Training in Elite Youth Football Players: Implications for Athlete Health and Performance

A study testing French Contrast Training + Standard football training (8 weeks) in people with Athletic Performance and Neuromuscular Adaptations, run by Gümüşhane Universıty at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This randomized controlled trial aimed to investigate the effects of an 8-week French Contrast Training (FCT) intervention on reactive strength index (RSI), sprint performance, and anaerobic profile in elite youth football players Read more about this study

Who is it for?
Ages 18 to 25 years, men onlyHealthy volunteers can take part
What is being tested?
French Contrast Training + Standard football training (8 weeks)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
28 participants
Where
1 siteTurkey (Türkiye)
Study dates
10 Apr 2026to 30 Jun 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 25 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Minimum 3 years football training
  • ≥80% training attendance
  • Injury-free for 6 months
  • Licensed academy player

Who cannot join

  • Musculoskeletal injury
  • Neurological disorder
  • Additional training programs
  • Ergogenic aid use

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Gumushane Univetsity

    Gümüşhane, Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane, 29600

Other trials in Turkey (Türkiye)

About this study

This randomized controlled trial aimed to investigate the effects of an 8-week French Contrast Training (FCT) intervention on reactive strength index (RSI), sprint performance, and anaerobic profile in elite youth football players

Read the detailed description

This study was designed as a parallel-group, randomized controlled trial to evaluate the chronic effects of French Contrast Training on neuromuscular performance and anaerobic capacity. A total of 28 elite male youth football players were randomly assigned to experimental and control groups. The intervention lasted 8 weeks, with performance assessments conducted pre- and post-intervention.

Being tested
French Contrast Training + Standard football training (8 weeks), Control
Keywords
Football, French Contrast Training, PAPE, Reactive Strength Index, Anaerobic Power

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • French Contrast Training + Standard football training (8 weeks)Other

    Also called French Contrast Training

    Participants in the experimental group performed French Contrast Training twice per week for 8 weeks, including heavy resistance, plyometric, loaded power, and assisted exercises.

  • ControlOther

    Also called Standard football training

    Standard football training

Study groups in NCT07511348
Study groupRoleWhat they receive
French Contrast Training + Standard football training (8 weeks)ExperimentalParticipants in the experimental group performed French Contrast Training twice per week for 8 weeks, including heavy resistance, plyometric, loaded power, and assisted exercises.
Receives: Other: French Contrast Training + Standard football training (8 weeks); Other: Control
Control GroupNo interventionStandard football training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Reactive Strength Index

    The pre-test and post-test Relative Strength Index (RSI) values of the sample group were obtained using the countermovement jump (CMJ) test. Participants started from an upright standing position on the platform with their feet shoulder-width apart and hands placed on their hips to eliminate arm swing. From this position, they were instructed to perform a rapid downward movement by flexing the hips and knees, immediately followed by a maximal vertical jump without any pause between the eccentric and concentric phases. Participants were required to keep their hands on their hips throughout the movement and to take off and land with both feet while attempting to jump as high as possible.

    Measured: 8 weeks

  2. Anaerobic Power

    Anaerobic profile (anaerobic capacity and fatigue index values) of the football players were assessed using a mechanically braked cycle ergometer connected to a computer and compatible software Wingate 894E test system. Prior to testing, the saddle height and pedal position were individually adjusted for each athlete to ensure an approximately 10% knee flexion angle at the lowest pedal position. After entering the athletes' descriptive information into the computer, the resistance load was automatically calculated by the system as 75 g per kg of body mass and subsequently applied to the ergometer's braking mechanism

    Measured: 8 week

Secondary outcomes (2)
  1. Sprint Performance (10-meter)

    The 10-meter sprint performance of the football players was assessed using a photocell timing system (Optojump, Microgate, Italy). Two pairs of photocells connected to an electronic timing system with dual-beam functionality and a measurement accuracy of ±0.001 s were positioned at the start and finish lines along a straight 10-meter track, with the sensors mounted 90 cm above the ground to ensure precise detection of the participants' movements. Participants began each trial from a standing start position, with one foot placed slightly forward, positioned 50 cm behind the starting photocell gate to standardize the initial stance.

    Measured: 8 week

  2. Fatigue Index

    Wingate Test

    Measured: 8 week

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Apr 2026
  2. Study start10 Apr 2026
  3. Primary completion25 Jun 2026
  4. Study completion30 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
This randomized controlled trial aimed to investigate the effects of an 8-week French Contrast Training (FCT) intervention on reactive strength index (RSI), sprint performance, and anaerobic profile in elite youth football players.
Masking
Double blind
Who is masked
Care provider, Outcomes assessor
Enrolment
28 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07511348
Sponsor's protocol ID
E-95674917-108.99-379723
Acronym
Unlocking PAPE
Status last verified
Oct 2026
First submitted
28 Mar 2026
Last updated
16 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data (IPD) will not be shared to protect participant privacy and in accordance with institutional ethical guidelines.

Questions about this trial

What is this clinical trial studying?

A study testing French Contrast Training + Standard football training (8 weeks) in people with Athletic Performance and Neuromuscular Adaptations, run by Gümüşhane Universıty at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Reactive Strength Index (time frame: 8 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Oct 2026.

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