- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07511348
Unlocking PAPE in Football: Effects of Eight Weeks of French Contrast Training on RSI, Sprint Performance, and Anaerobic Profile (Unlocking PAPE)
April 3, 2026 updated by: Coşkun YILMAZ, Gümüşhane Universıty
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
Study Overview
Status
Completed
Conditions
Intervention / Treatment
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.
Study Type
Interventional
Enrollment (Actual)
28
Phase
- Not Applicable
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
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Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane
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Gümüşhane, Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane, Turkey (Türkiye), 29600
- Gumushane Univetsity
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-
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
Description
Inclusion Criteria:
- Minimum 3 years football training
- ≥80% training attendance
- Injury-free for 6 months
- Licensed academy player
Exclusion Criteria:
- Musculoskeletal injury
- Neurological disorder
- Additional training programs
- Ergogenic aid use
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
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: French Contrast Training + Standard football training (8 weeks)
Participants in the experimental group performed French Contrast Training twice per week for 8 weeks, including heavy resistance, plyometric, loaded power, and assisted exercises.
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Participants in the experimental group performed French Contrast Training twice per week for 8 weeks, including heavy resistance, plyometric, loaded power, and assisted exercises.
Other Names:
Standard football training
Other Names:
|
|
No Intervention: Control Group
Standard football training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anaerobic Power
Time Frame: 8 week
|
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
|
8 week
|
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Reactive Strength Index
Time Frame: 8 weeks
|
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.
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8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Fatigue Index
Time Frame: 8 week
|
Wingate Test
|
8 week
|
|
Sprint Performance (10-meter)
Time Frame: 8 week
|
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.
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8 week
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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)
December 5, 2025
Primary Completion (Actual)
February 15, 2026
Study Completion (Actual)
February 20, 2026
Study Registration Dates
First Submitted
March 28, 2026
First Submitted That Met QC Criteria
March 28, 2026
First Posted (Actual)
April 6, 2026
Study Record Updates
Last Update Posted (Actual)
April 9, 2026
Last Update Submitted That Met QC Criteria
April 3, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- E-95674917-108.99-379723
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data (IPD) will not be shared to protect participant privacy and in accordance with institutional ethical guidelines.
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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