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Clinical Trials in Turkey / NCT07072715
Active, not recruiting Not applicable

Plyometrics vs PAPE Training in Football: Effects on Agility, Explosive Power and Speed

NCT07072715 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-06-01
Last updated
2025-07-18

Condition(s) studied

Athletic PerformanceFootball PlayersSports PerformanceSports Physical Therapy

Investigational drug(s) / intervention(s)

PAPE TrainingPlyometric Training

PAPE Training: A neuromuscular activation protocol involving heavy banded squats (\~85% 1RM) to induce post-activation performance enhancement. Applied three times weekly over 8 weeks following the warm-up. Participants then continued with regular football training.

Plyometric Training: A program of depth jumps designed to enhance explosive power, speed, and agility. Applied 3 times weekly over 8 weeks following the warm-up. Participants then continued with their regular football training.

Study summary

The goal of this clinical trial is to compare the effects of 8 week plyometric training and post-activation performance enhancement (PAPE) training on explosive power, agility, acceleration and sprint speed, muscle strength and flexibility in healthy male semi-professional football players aged 18-35.

The main questions it aims to answer are:

Does PAPE training have effects on performance metrics of football players when planned and applied long-term (8 weeks)?

Does long term PAPE training improve agility, acceleration and speed, flexibility, vertical jump height, and muscle strength more effectively than Plyometric training?

Is there a significant difference in performance gains between PAPE and plyometric training compared to a control group receiving only routine football training?

Researchers will compare a plyometric training group, a PAPE training group, and a control group to determine which method most effectively enhances football-specific performance outcomes.

Participants will:

* Be randomly assigned to one of three groups (Plyometric, PAPE, or Control)
* Continue their routine football training as usual
* Receive additional training sessions applied immediately after warm-up and before continuing regular team training alongside the Control group (for PAPE and Plyometric group)
* Undergo an 8-week training program (3 times per week for Plyometric and PAPE groups)

Assessments will be conducted at baseline, week 4, and week 8, including:

* Vertical Jump Test (explosive power)
* 30-Meter Sprint Test, including 10-meter acceleration recording
* Illinois Agility Test
* Isometric strength measurements of quadriceps, hamstrings, and gastrocnemius using a handheld dynamometer
* Sit and Reach Test and Modified Thomas Test (flexibility)

In addition, all participants will complete a sociodemographic and lifestyle assessment form capturing:

Age, height, weight, BMI Football experience and playing position Education level, employment status Sleep duration, training frequency, and training intensity Smoking and alcohol use status.

Eligibility

Sex
MALE
Min age
18 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Male athletes aged between 18 and 35 years * Permission obtained from the team physician to participate in the study * Active participation in a Semi-Professional football team for at least the past 6 months * Participating in football training at least 3 times per week * Willing and able to participate in 8-week training and testing protocol voluntarily Exclusion Criteria: * Current or recent surgery affecting the lower limbs * Current or recent injury affecting the lower limbs * History of neurological, cardiovascular, orthopedic or systemic disease * Inconsistent football training (\<3x per week) * Failure to attend testing or training sessions

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Fatih Karagümrük A.Ş. Istanbul Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07072715 on ClinicalTrials.gov ↗ ← All trials in Turkey