- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07755345
Weighted vs Unweighted Plyometric Conditioning on Vertical Jump Performance in Young Male Soccer Players (PAPE-JUMP)
Differential Time-Course Effects of Weighted and Unweighted Plyometric Conditioning on Vertical Jump Performance in Young Male Soccer Players
Explosive lower-limb power is essential for soccer performance and contributes to jumping, sprinting, and rapid changes of direction. Plyometric exercises are commonly used during warm-up to improve neuromuscular readiness and may enhance subsequent athletic performance through post-activation performance enhancement (PAPE). However, it remains unclear whether adding external load during plyometric conditioning provides greater benefits than performing the same exercises without additional load.
The purpose of this study is to compare the acute effects of weighted and unweighted plyometric conditioning on vertical jump performance in young male soccer players. Participants complete two experimental sessions separated by 48 hours. In one session, they perform a standardized single-leg plyometric protocol without external load, and in the other session they perform the same protocol while wearing a weighted vest equivalent to 10% of their body mass. Vertical jump height is assessed before exercise and at several time points after the conditioning activity to examine the time course of performance changes.
The findings of this study are expected to improve understanding of the optimal use of weighted plyometric conditioning during warm-up and provide practical guidance for coaches and sports practitioners seeking to maximize explosive performance before training and competition.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Istanbul
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Istanbul, Istanbul, Turkey (Türkiye), 34290
- Istanbul Gelisim University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy male soccer players aged 18 to 30 years.
- Actively participating in organized soccer training.
- Minimum of 2 years of structured plyometric training experience.
- Competing at the regional development league level.
- Free from lower-limb musculoskeletal injury during the previous 4 months.
- Able to perform maximal jumping tasks.
- Provided written informed consent prior to participation.
Exclusion Criteria:
- History of lower-extremity surgery within the previous year.
- Current lower-limb pain or discomfort during jumping activities.
- Neurological, cardiovascular, or orthopedic disorders affecting neuromuscular performance.
- Use of performance-enhancing substances.
- Failure to comply with study procedures or testing instructions.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Weighted Plyometric Conditioning
Participants performed a standardized single-leg plyometric conditioning protocol while wearing a weighted vest equivalent to 10% of their body mass.
Vertical jump performance was assessed at baseline and at 15 seconds, 2 minutes, 4 minutes, and 8 minutes after the conditioning activity.
|
Participants completed three sets of ten single-leg plyometric repetitions while wearing a weighted vest corresponding to 10% of their body mass.
Sessions were separated by 48 hours, and jump performance was measured before and after the conditioning protocol.
|
|
Active Comparator: Unweighted Plyometric Conditioning
Participants performed the same standardized single-leg plyometric conditioning protocol without external load.
Vertical jump performance was assessed at baseline and at 15 seconds, 2 minutes, 4 minutes, and 8 minutes after the conditioning activity.
|
Participants completed the identical single-leg plyometric conditioning protocol without external load.
Vertical jump performance was measured before and after the conditioning protocol using the same assessment schedule.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Vertical Jump Height
Time Frame: Baseline, 15 seconds, 2 minutes, 4 minutes, and 8 minutes after each intervention session
|
Vertical jump height (cm) measured before the plyometric conditioning protocol (baseline) and at 15 seconds, 2 minutes, 4 minutes, and 8 minutes after weighted and unweighted plyometric conditioning.
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Baseline, 15 seconds, 2 minutes, 4 minutes, and 8 minutes after each intervention session
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Area Under the Curve (AUC) of Vertical Jump Performance
Time Frame: Immediately after completion of each intervention session
|
Cumulative vertical jump performance across the post-activation period.
|
Immediately after completion of each intervention session
|
|
Performance Slope
Time Frame: Immediately after completion of each intervention session
|
Rate of change in vertical jump height across the post-activation period.
|
Immediately after completion of each intervention session
|
|
Peak Vertical Jump Height
Time Frame: 15 seconds to 8 minutes after each intervention session
|
Highest vertical jump height achieved during the post-activation assessment period.
|
15 seconds to 8 minutes after each intervention session
|
|
Time to Peak Performance
Time Frame: 15 seconds to 8 minutes after each intervention session
|
Time required to reach the highest vertical jump performance following each conditioning protocol.
|
15 seconds to 8 minutes after each intervention session
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- PAPE-PLYO-2025-01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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