- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07705087
Impact of Plyometric Training Methods on Athletic Performance and Detraining Processes in Youth Female Soccer Players
July 10, 2026 updated by: Fatih GUR, Pamukkale University
Lower extremity strength, explosive power, dynamic balance, and functional range of motion are critical determinants of athletic performance and injury prevention in soccer (football).
While plyometric training is widely used to improve these qualities, the comparative effects of bodyweight plyometric training versus externally loaded plyometric training, and the maintenance of these effects during detraining periods, remain unclear.
This study aims to investigate the effects of two different plyometric training methods on athletic performance and subsequent detraining processes in young female soccer players.
Participants will be randomly assigned to three groups: Bodyweight Plyometric Training Group (BW-PT), External Loading Plyometric Training Group (EL-PT, who will wear vests weighing 10% of their body weight), and Control Group (CG, who will only continue with routine soccer training).
Training interventions will be conducted for 6 weeks, immediately followed by a 4-week detraining period.
To comprehensively assess athletic performance, the following measurements will be taken at baseline (pre-test), immediately after the training period (post-test), and after the detraining period (maintenance test): Isokinetic muscle strength of knee extensors and flexors (peak torque and force development rate at 60°/s and 120°/s), Jumping performance (standing long jump, vertical jump height, and 15-second repeated jump test), Functional range of motion (via Functional Movement Screen - FMS), Dynamic balance (via Y-Balance Test).
The primary objective is to determine which plyometric loading strategy, compared to traditional soccer training, provides superior and longer-lasting physiological and biomechanical adaptations in young female athletes.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
36
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 Contact
- Name: Fatih GUR, PhD
- Phone Number: +90 258 236 14 88
- Email: fatihgur@pau.edu.tr
Study Locations
-
-
Denizli
-
Denizli, Denizli, Turkey (Türkiye), 20160
- Pamukkale University, Faculty of Sport Sciences
-
Contact:
- Fatih GUR, PhD
- Phone Number: +90 258 296 14 88
- Email: fatihgur@pau.edu.tr
-
-
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
- Child
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- No history of surgery due to musculoskeletal injuries within the past 6 months.
- No use of ergogenic supplements within the past 3 months.
- Regular participation in routine team training sessions for at least 2 months prior to the study.
Exclusion Criteria:
- History of any recent injury requiring a recovery period of more than one week.
- Use of ergogenic aids or nutritional supplements during the intervention period.
- Missing two consecutive or four non-consecutive training sessions during the study period.
- Participation in additional structured physical training or exercises outside of the routine team practices and the study protocol.
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: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Body-Weight Plyometric Training Group
Participants in this group will perform plyometric training using only their own body weight.
|
A structured plyometric training program performed twice a week for six weeks.
Exercises include various jumps and bounds using only the participant's body weight.
Each session lasts approximately 30 minutes.
|
|
Experimental: Plyometric Training Group With Additional Load
Participants in this group will perform plyometric training while wearing a weighted vest equal to 10% of their body weight.
|
A structured plyometric training program performed twice a week for six weeks.
Participants will wear a weighted vest equivalent to 10% of their body weight during the exercises.
Each session lasts approximately 30 minutes.
|
|
Active Comparator: Control Group
Participants in this group will continue their routine football training without any additional plyometric exercises.
|
Participants in this group will continue to perform their standard, routine football training sessions.
They will not receive any additional or structured plyometric training program during the intervention period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Absolute Peak Torque (APT) of Knee Extensors and Flexors
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Concentric isokinetic absolute peak torque (APT) of the knee extensors and flexors (dominant leg) will be evaluated at 60°/s and 120°/s angular velocities using a Cybex Humac Norm dynamometer during 5 maximal repetitions.
(Unit of measure: Nm)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
|
Relative Peak Torque (RPT) of Knee Extensors and Flexors
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Concentric isokinetic relative peak torque (RPT) of the knee extensors and flexors (dominant leg) will be evaluated at 60°/s and 120°/s angular velocities using a Cybex Humac Norm dynamometer during 5 maximal repetitions.
(Unit of measure: Nm/kg)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
|
Time to Peak Torque (TPT) of Knee Extensors and Flexors
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Concentric isokinetic time to peak torque (TPT) of the knee extensors and flexors (dominant leg) will be evaluated at 60°/s and 120°/s angular velocities using a Cybex Humac Norm dynamometer during 5 maximal repetitions.
(Unit of measure: milliseconds)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
|
Average Peak Torque (AvPT) of Knee Extensors and Flexors
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Concentric isokinetic average peak torque (AvPT) of the knee extensors and flexors (dominant leg) will be evaluated at 60°/s and 120°/s angular velocities using a Cybex Humac Norm dynamometer during 5 maximal repetitions.
(Unit of measure: Nm)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
|
Average Rate of Force Development (AvRFD) of Knee Extensors and Flexors
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Concentric isokinetic average rate of force development (AvRFD) of the knee extensors and flexors (dominant leg) will be evaluated at 60°/s and 120°/s angular velocities using a Cybex Humac Norm dynamometer during 5 maximal repetitions.
(Unit of measure: Nm/s)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
|
Vertical Jump Height (VJH)
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Vertical jump height calculated from flight time will be evaluated using an electronic contact mat system (Fusion SmartJump, Fusion Sport, Australia).
Participants will perform a countermovement jump without arm swing.
The best value from 3 repetitions, separated by 1-minute rest intervals, will be recorded.
(Unit of measure: cm)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
|
Standing Long Jump (SLJ) Distance
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Horizontal jump distance will be assessed.
Participants will perform a maximum distance jump with two feet from behind a starting line.
The best value from 3 repetitions will be recorded.
(Unit of measure: cm)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
|
15-Second Repeated Jump Test: Average Power (RJ15s-AP)
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Average power (RJ15s-AP) will be evaluated during 15 seconds of continuous maximal vertical jumps using an electronic contact mat system (Fusion SmartJump, Fusion Sport, Australia).
Participants will jump with hands on hips and an upright trunk.
The value is calculated using the Bosco equation.
(Unit of Measure: W)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
|
15-Second Repeated Jump Test: Flight Time (RJ15s-FT)
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Flight time (RJ15s-FT) will be evaluated during 15 seconds of continuous maximal vertical jumps using an electronic contact mat system (Fusion SmartJump, Fusion Sport, Australia).
Participants will jump with hands on hips and an upright trunk.
The value is calculated using the Bosco equation.
(Unit of Measure: ms)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
|
15-Second Repeated Jump Test: Number of Jumps (N-RJ15s)
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
The number of jumps (N-RJ15s) will be evaluated during 15 seconds of continuous maximal vertical jumps using an electronic contact mat system (Fusion SmartJump, Fusion Sport, Australia).
Participants will jump with hands on hips and an upright trunk.
(Unit of Measure: Count)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional Movement Capacity
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Functional movement capacity and potential asymmetries will be evaluated using the Functional Movement Screen (FMS) kit, which consists of 7 movement patterns scored from 0 to 3 (max total score: 21).
(Unit of measure: Score on a scale from 0 to 21)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
|
Dynamic Balance and Neuromuscular Control
Time Frame: Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Dynamic balance will be measured using the Y-Balance Test kit.
Reach distances in three directions will be normalized to the participant's leg length to assess lower extremity neuromuscular control and asymmetry.
(Unit of measure: Percentage)
|
Baseline (Week 0), immediately post-training (Week 6), and after the detraining period (2nd and 4th week).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: GUR, Pamukkale University
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 (Estimated)
July 20, 2026
Primary Completion (Estimated)
October 19, 2026
Study Completion (Estimated)
October 19, 2026
Study Registration Dates
First Submitted
July 2, 2026
First Submitted That Met QC Criteria
July 10, 2026
First Posted (Actual)
July 15, 2026
Study Record Updates
Last Update Posted (Actual)
July 15, 2026
Last Update Submitted That Met QC Criteria
July 10, 2026
Last Verified
July 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- E-60116787-020-811428
- 2026TAP009 (Other Grant/Funding Number: Pamukkale University Scientific Research Projects Coordination Unit)
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.
The informed consent obtained from the participants does not include provisions for public data sharing.
Furthermore, preserving the privacy and complete anonymization of the participants in this small, cohort-specific sports science study is a priority, which restricts the feasibility of sharing individual-level data.
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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