Micro-Dosed vs. Traditional Plyometric Training in Elite Youth Soccer
TRMD-PLYO_U19
A Volume-Matched Quasi-Experimental Trial Comparing Micro-Dosed and Traditional Plyometric Training on Speed and Explosive Abilities in Elite Under-19 Soccer Players During the Pre-Season
1 other identifier
interventional
24
1 country
1
Brief Summary
The goal of this clinical trial is to learn if a micro-dosed plyometric training program works as well as a traditional plyometric program for improving speed and explosive abilities in elite under-19 soccer players during the pre-season. The main questions are:
- Traditional Training Group: 2 sessions per week, about 40 minutes each.
- Micro-dosed Group: 3-4 shorter sessions per week, about 20 minutes each. Both groups will complete the same total weekly training volume. Participants will:
- Take part in an 8-week plyometric training program during pre-season.
- Complete performance tests (CM jump tests, a 30-meter sprint, and a 15-0-5 change-of-direction test, broad jump test, drop jump test) before and after 8-week plyometric intervention, . This study will help coaches and players understand if shorter, more frequent plyometric training sessions can be a good alternative to traditional longer sessions when weekly training load is matched.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 8, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 10, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
September 17, 2024
CompletedFirst Submitted
Initial submission to the registry
September 18, 2025
CompletedFirst Posted
Study publicly available on registry
September 26, 2025
CompletedSeptember 26, 2025
September 1, 2025
2 months
September 18, 2025
September 18, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Change in countermovement jump (CMJ) jump height
Change in vertical jump height (cm) measured with dual force plates during a countermovement jump, from baseline (pre-test) to post-intervention (8 weeks).
Baseline and after 8 weeks of intervention.
Change in Sprint Speed (30 m sprint test using 1080 Sprint system)
Change in sprint velocity (m/s) and split times (0-5 m, 0-10 m, 0-30 m).
Baseline and after 8 weeks of intervention.
Change in Drop Jump Reactive Strength Index (RSI)
Change in reactive strength index (jump height / ground contact time) measured during drop jump from 30 cm platform.
Baseline and after 8 weeks.
Secondary Outcomes (3)
Change in Standing Broad Jump Distance (SBJ)
Baseline and after 8 weeks.
Change in Sprint Mechanics (1080 Sprint)
Baseline and after 8 weeks.
Change in Change-of-Direction Performance (15-0-5 test)
Baseline and after 8 weeks.
Study Arms (2)
Traditional Plyometric Training Group
ACTIVE COMPARATORParticipants in this group completed a traditional plyometric training program during the 8-week pre-season period. The program consisted of 2 sessions per week, each lasting about 40 minutes. Exercises included countermovement jumps, drop jumps, broad jumps, and other standard plyometric drills. The total weekly training volume was matched to the micro-dosed group.
Micro-dosed Plyometric Training Group
EXPERIMENTALParticipants in this group completed a micro-dosed plyometric training program during the 8-week pre-season period. The program consisted of 3 to 4 shorter sessions per week, each lasting about 20 minutes. The same types of plyometric exercises were used as in the traditional group (e.g., countermovement jumps, drop jumps, broad jumps). The total weekly training volume was matched to the traditional group.
Interventions
This intervention consists of two supervised plyometric training sessions per week, each lasting about 40 minutes. It represents the traditional approach with fewer but longer sessions. The total weekly training volume is equivalent to the micro-dosed group but distributed differently.
This intervention consists of three to four shorter supervised plyometric sessions per week, each lasting about 20 minutes. It represents a micro-dosed approach, with higher frequency but shorter duration per session. The total weekly training volume is equivalent to the traditional group but distributed across more frequent sessions.
Eligibility Criteria
You may qualify if:
- Active membership in a U19 elite soccer club during the intervention.
- Medical fitness to participate in plyometric training and testing.
- Attendance at ≥75% of training sessions.
- Completion of all mandatory pre- and post-tests.
- Previous experience with plyometric training and testing procedures.
You may not qualify if:
- Medical limitations preventing safe participation in training or testing.
- Attendance lower than 75% of scheduled intervention sessions.
- Failure to complete mandatory baseline or follow-up testing.
- Injury preventing completion of the intervention.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Matej Bel Universitylead
- Masaryk Universitycollaborator
Study Sites (1)
Masaryk University
Brno, Czechia
Related Publications (6)
Afonso J, Nakamura FY, Baptista I, Rendeiro-Pinho G, Brito J, Figueiredo P. Microdosing: Old Wine in a New Bottle? Current State of Affairs and Future Avenues. Int J Sports Physiol Perform. 2022 Oct 6;17(11):1649-1652. doi: 10.1123/ijspp.2022-0291. Print 2022 Nov 1.
PMID: 36202386BACKGROUNDCuadrado-Penafiel V, Castano-Zambudio A, Martinez-Aranda LM, Gonzalez-Hernandez JM, Martin-Acero R, Jimenez-Reyes P. Microdosing Sprint Distribution as an Alternative to Achieve Better Sprint Performance in Field Hockey Players. Sensors (Basel). 2023 Jan 6;23(2):650. doi: 10.3390/s23020650.
PMID: 36679451BACKGROUNDWang J, Wang Y, Jiang Y, Li S, Jia X, Xiao X, Sun W, Wang P, Zhang Q. Datasets-Based IMPDH1 Revisited: Heterozygous Missense Variants for Dominant Retinitis Pigmentosa While Truncation Variants Are Likely Non-Pathogenic. Curr Eye Res. 2024 Aug;49(8):853-861. doi: 10.1080/02713683.2024.2336158. Epub 2024 Apr 11.
PMID: 38604988BACKGROUNDDiStefano LJ, Martinez JC, Crowley E, Matteau E, Kerner MS, Boling MC, Nguyen AD, Trojian TH. Maturation and Sex Differences in Neuromuscular Characteristics of Youth Athletes. J Strength Cond Res. 2015 Sep;29(9):2465-73. doi: 10.1519/JSC.0000000000001052.
PMID: 26313573BACKGROUNDLiu G, Wang X, Xu Q. Microdosing Plyometric Training Enhances Jumping Performance, Reactive Strength Index, and Acceleration among Youth Soccer Players: A Randomized Controlled Study Design. J Sports Sci Med. 2024 Jun 1;23(2):342-350. doi: 10.52082/jssm.2024.342. eCollection 2024 Jun.
PMID: 38841635BACKGROUNDNuzzo JL, Pinto MD, Kirk BJC, Nosaka K. Resistance Exercise Minimal Dose Strategies for Increasing Muscle Strength in the General Population: an Overview. Sports Med. 2024 May;54(5):1139-1162. doi: 10.1007/s40279-024-02009-0. Epub 2024 Mar 20.
PMID: 38509414BACKGROUND
Study Officials
- STUDY CHAIR
Martin Pupiš
Faculty of Sport Science and Health, Matej Bel University
- PRINCIPAL INVESTIGATOR
Marián Škorik
Faculty of Sport Science and Health, Matej Bel University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Masking Details
- Masking was not feasible due to the visible differences in training frequency and scheduling.
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD Candidate, Faculty of Sports Science and Health, Matej Bel University
Study Record Dates
First Submitted
September 18, 2025
First Posted
September 26, 2025
Study Start
July 8, 2024
Primary Completion
September 10, 2024
Study Completion
September 17, 2024
Last Updated
September 26, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ANALYTIC CODE
- Time Frame
- Data and supporting information will be available beginning 12 months after article publication. Data will remain available for at least 5 years after publication.
- Access Criteria
- Qualified researchers will be able to request access to the de-identified dataset and supporting materials by contacting the corresponding author. Access will be granted for scientific purposes only and in accordance with institutional and ethical guidelines.
De-identified individual participant data (IPD), including pre- and post-intervention performance outcomes (e.g., jump height, reactive strength index, sprint performance, change-of-direction test results), will be shared. No personally identifying information will be included. Data will be shared through an open repository such as OSF (Open Science Framework) or Zenodo. The link will be provided upon availability.