Effects of Velocity-Based and Traditional Resistance Training on Performance in Trained Male Football Players (VBRT-TRT-FP)

June 11, 2026 updated by: Ahmet Mor, Sinop University

Effects of Velocity-Based and Traditional Resistance Training on Physical Performance, Anaerobic Capacity, and Perceptual Responses in Trained Male Football Players

This study compared the effects of velocity-based resistance training (VBRT) and traditional resistance training (TRT) on physical performance, anaerobic capacity, and perceptual responses in trained male football players. Sixteen participants were randomly assigned to either a VBRT group or a TRT group and completed an 8-week resistance training program. The study aimed to determine whether VBRT provides greater improvements in explosive performance, anaerobic power, balance, football-specific performance, and fatigue-related perceptions compared with traditional percentage-based resistance training.

Study Overview

Detailed Description

Resistance training is widely used in football to improve strength, power, and sport-specific performance. Traditional resistance training typically prescribes training loads based on fixed percentages of one-repetition maximum (1RM). However, this approach may not adequately account for daily fluctuations in neuromuscular readiness and fatigue. Velocity-based resistance training (VBRT) has emerged as an alternative method that uses movement velocity to individualize training load and regulate training effort.

The purpose of this study was to compare the effects of velocity-based resistance training and traditional percentage-based resistance training in trained male football players. Participants were randomly assigned to either a VBRT group or a traditional resistance training (TRT) group and completed an 8-week resistance training intervention consisting of deep squat, half squat, and bench press exercises performed twice weekly.

In the VBRT group, training loads were adjusted using individualized load-velocity profiles and velocity-loss thresholds, whereas the TRT group trained using fixed percentages of baseline one-repetition maximum values. The study was designed to evaluate whether individualized velocity-based load prescription could improve neuromuscular performance and fatigue management compared with traditional resistance training methods.

The findings of this study may contribute to the understanding of practical resistance training strategies for football players and provide information regarding the effectiveness of velocity-based training for improving performance-related and fatigue-related adaptations.

Study Type

Interventional

Enrollment (Actual)

16

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 Locations

    • Sinop
      • Sinop, Sinop, Turkey (Türkiye), 57000
        • Sinop University, Faculty of Sport Sciences

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male football players aged 18 to 25 years
  • Actively participating in organized football training and competition
  • At least 1 year of structured resistance training experience
  • Regular exposure to football-specific training loads
  • Willing and able to provide written informed consent

Exclusion Criteria:

  • Musculoskeletal injury within the previous 6 months
  • Neurological, orthopedic, or chronic disorders affecting physical performance
  • Use of ergogenic aids or supplements that could influence neuromuscular performance
  • Participation in additional resistance training outside the study protocol
  • Missing more than 10% of the scheduled training sessions

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: Velocity-Based Resistance Training (VBRT)
Participants completed an 8-week velocity-based resistance training program consisting of deep squat, half squat, and bench press exercises performed twice weekly. Training loads were prescribed using individualized load-velocity profiles and adjusted according to target movement velocities and a 20% velocity-loss threshold.
Participants completed an 8-week velocity-based resistance training program performed twice weekly. Training consisted of deep squat, half squat, and bench press exercises. Training loads were prescribed using individualized load-velocity profiles and adjusted according to target movement velocities and a 20% velocity-loss threshold.
Experimental: Traditional Resistance Training (TRT)
Participants completed an 8-week traditional percentage-based resistance training program consisting of deep squat, half squat, and bench press exercises performed twice weekly. Training loads were prescribed using fixed percentages of baseline one-repetition maximum values and were not adjusted according to daily performance fluctuations.
Participants completed an 8-week traditional percentage-based resistance training program performed twice weekly. Training consisted of deep squat, half squat, and bench press exercises. Training loads were prescribed using fixed percentages of baseline one-repetition maximum values.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change From Baseline in Vertical Jump Height at 8 Weeks
Time Frame: Baseline and Week 8
Vertical jump height (cm) measured using a digital vertical jump device to assess lower-body explosive performance.
Baseline and Week 8

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Actual)

December 15, 2025

Primary Completion (Actual)

February 18, 2026

Study Completion (Actual)

February 18, 2026

Study Registration Dates

First Submitted

June 11, 2026

First Submitted That Met QC Criteria

June 11, 2026

First Posted (Actual)

June 17, 2026

Study Record Updates

Last Update Posted (Actual)

June 17, 2026

Last Update Submitted That Met QC Criteria

June 11, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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