- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07418892
Effects of Resisted Versus Unresisted Sprint Training on Sprint Force-Velocity Profile in Youth Footballers (RST-FV Youth F)
Effects of Resisted Versus Non-resisted Sprint Training on Countermovement Jump and Sprint Force-velocity Profile in Youth Footballers: a Randomised Controlled Trial
This randomised, controlled, two-arm trial evaluates whether light resisted sprint training (sled towing at 20% of body mass) produces superior improvements in 30 m sprint mechanical outputs compared with matched-dose unresisted sprint training in youth footballers.
Participants complete two supervised sessions per week for six consecutive weeks, integrated into normal academy microcycles on the same artificial-turf surface. Primary outcomes are changes in sprint-derived force-velocity-power profile parameters and 30 m sprint performance, with secondary outcomes including countermovement jump height and anthropometrics.
Study Overview
Status
Intervention / Treatment
Detailed Description
The study uses a parallel-group randomised design. Allocation is stratified by squad category (Under-14 and Juvenile) with simple randomisation within strata using computer-generated random numbers prepared by a researcher not involved in training delivery.
The intervention is delivered on a third-generation artificial-turf pitch at a youth academy integrated within a professional development pathway. Forty-four outfield players from two squads are enrolled.
Both arms complete 20 m maximal sprints with identical volume and rest structure (3 sets × 5 repetitions, 45 s inter-repetition rest, 3 min inter-set rest). The experimental arm performs sled towing at 20% body mass (sled tare 3 kg plus plates), whereas the comparator arm performs unresisted maximal sprints. No additional lower-limb strength or speed work beyond the head coach's standard plan is introduced during the intervention period.
Primary outcomes are derived from 30 m sprint profiling, using high-speed video and the MySprint application to compute split times and estimate sprint mechanical variables within the Morin-Samozino framework. Outcome assessors/video analysts and the statistician are blinded to group codes, while full participant blinding is not feasible due to the presence of the sled.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Antioquia
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Medellín, Antioquia, Colombia, 054080
- Universidad de Antioquia
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male football (soccer) player aged 13 to 17 years.
- Registered Under-14 or Juvenile player in an organized football program/club/league.
- At least 1 year of organized football experience.
- Current health-system affiliation (e.g., EPS).
- Provided informed assent; parent/guardian provided written informed consent (for minors).
- Able to attend and comply with the sessional training and testing protocol.
Exclusion Criteria:
- Current musculoskeletal complaint or injury at baseline.
- Ongoing rehabilitation at baseline.
- Logistical constraints preventing participation in the sessional protocol (e.g., inability to attend required sessions/assessments).
- Injury incurred during the intervention that prevents safe continuation (participant will be withdrawn).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Resisted Sprint Training (RST)
20 m maximal sprints towing a sled loaded to 20% of individual body mass (sled tare 3 kg; plates added).
3 sets × 5 repetitions, 45 s inter-rep rest, 3 min inter-set rest; two supervised sessions/week for six weeks, conducted at the start of squad training, on the same artificial-turf surface.
|
20 m maximal sprints towing a sled loaded to 20% of individual body mass (sled tare 3 kg; plates added).
3 sets × 5 repetitions, 45 s inter-rep rest, 3 min inter-set rest; two supervised sessions/week for six weeks, conducted at the start of squad training, on the same artificial-turf surface.
|
|
Active Comparator: Unresisted Sprint Training
20 m maximal sprints without external resistance; dose and rest schedule identical to RST (3 × 5 × 20 m; 45 s; 3 min); two sessions/week for six weeks; same surface and session placement; standard team training continues.
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20 m maximal sprints without external resistance; dose and rest schedule identical to RST (3 × 5 × 20 m; 45 s; 3 min); two sessions/week for six weeks; same surface and session placement; standard team training continues.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline to post-intervention in best 30 m sprint time
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Best (fastest) 30 m sprint time, expressed in seconds (s).
The reported value is the best 30 m time (s).
|
From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline to post-intervention in theoretical maximal horizontal force (F0)
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
|
Sprint-derived theoretical maximal horizontal force (F0), expressed relative to body mass (N/kg).
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From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
|
|
Change from baseline to post-intervention in peak sprint velocity
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Peak velocity reached during the sprint assessment, expressed in meters per second (m/s).
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From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
|
|
Change from baseline to post-intervention in rate of decrease in RF with velocity (DRF)
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Sprint-derived rate of decrease in RF with velocity (DRF), expressed as % per m.
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From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
|
|
Change from baseline to post-intervention in peak ratio of horizontal force (RF_peak)
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
|
Sprint-derived peak ratio of horizontal force (RF_peak), expressed as percentage (%).
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From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Change from baseline to post-intervention in ratio of horizontal force (RF)
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Sprint-derived ratio of horizontal force (RF), expressed as percentage (%).
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From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Change from baseline to post-intervention in maximal horizontal power (Pmax)
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
|
Sprint-derived maximal horizontal power (Pmax), expressed relative to body mass (W/kg).
|
From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
|
|
Change from baseline to post-intervention in theoretical maximal running velocity (V0)
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Sprint-derived theoretical maximal running velocity (V0), expressed in meters per second (m/s).
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From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
|
|
Change from baseline to post-intervention in countermovement jump (CMJ) height
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Countermovement jump (CMJ) height, expressed in centimeters (cm).
The reported value is CMJ height (cm).
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From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline to post-intervention in stature (standing height)
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Stature (standing height), expressed in centimeters (cm).
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From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Change from baseline to post-intervention in body mass
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Body mass, expressed in kilograms (kg).
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From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Change from baseline to post-intervention in body mass index (BMI)
Time Frame: From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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BMI calculated as body mass (kg) divided by stature squared (m^2), expressed as kg/m^2.
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From baseline assessment (within 1 week prior to first training session) to post-intervention assessment (within 1 week after the final training session), over the 6-week intervention period.
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Collaborators and Investigators
Sponsor
Collaborators
Publications and helpful links
General Publications
- Young, J. D., Whitten, J., Reid, J., Quigley, P. J., Low, J., Li, Y., Lima, C., Hodgson, D., Chaouachi, A., Prieske, O., & Granacher, U. (2017). Effectiveness of Traditional Strength vs. Power Training on Muscle Strength, Power and Speed with Youth: A Systematic Review and Meta-Analysis. Frontiers. https://doi.org/10.3389/fphys.2017.0042
- Baena-Raya, A., García-Mateo, P., García-Ramos, A., Rodríguez-Pérez, M., & Soriano-Maldonado, A. (2021). Delineating the potential of the vertical and horizontal force-velocity profile for optimizing sport performance: A systematic review. Journal of Sports Sciences, 40, 331 - 344. https://doi.org/10.1080/02640414.2021.199364 Behm, D. G.,
- Bachero-Mena, B., & González-Badillo, J. (2014). Effects of Resisted Sprint Training on Acceleration With Three Different Loads Accounting for 5, 12.5, and 20% of Body Mass. Journal of Strength and Conditioning Research, 28, 2954-2960. https://doi.org/10.1519/jsc.000000000000049
- Aquino, R., Gonçalves, L. G., Galgaro, M., Maria, T. S., Rostaiser, E., Garcia, G. R., Neto, M. V. M., & Nakamura, F. Y. (2021). Mach running performance in Brazilian professional soccer players: comparisons between successful and unsuccessful teams. https://doi.org/10.31236/osf.io/jm579
- Amore, M., Minciacchi, D., Panconi, G., Guarducci, S., Bravi, R., & Sorgente, V. (2024). Impact of Sled-Integrated Resisted Sprint Training on Sprint and Vertical Jump Performance in Young U-14 Male Football Players. Journal of Functional Morphology and Kinesiology, 9. https://doi.org/10.3390/jfmk9040256
- Alcaraz, P. E., Carlos-Vivas, J., Oponjuru, B. O., & Martínez-Rodríguez, A. (2018). The Effectiveness of Resisted Sled Training (RST) for Sprint Performance: A Systematic Review and Meta-analysis. Sports Medicine, 48(9), 2143-2165. doi:10.1007/s40279-018-0947-8
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
Keywords
Other Study ID Numbers
- CE-042024-6-2024
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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