Game-Based Versus Linear Sprint Training in Male Soccer Players (GBS-LST)

August 28, 2026 updated by: Görkem Açar, Istanbul Gelisim University

A 12-Week Randomized Controlled Trial Evaluating the Time-Course Effects of Once-Weekly Game-Based Versus Linear Sprint Training on Soccer Performance and Hamstring Strength in Amateur Players During the Competitive Season

This randomized controlled trial investigated the effects of two different sprint training approaches on physical performance in male amateur soccer players during the competitive season. The study aimed to determine whether once-weekly game-based sprint training or linear sprint training could improve sprint performance, change-of-direction ability, hamstring strength, and maximum running velocity achieved during official matches.

Thirty-six male amateur soccer players were randomly assigned in a 1:1:1 ratio to one of three groups: the Game-Based Sprint Group, the Linear Sprint Group, or the Control Group. Participants in both sprint training groups completed one additional sprint training session per week for 12 weeks while continuing their regular soccer training and competition schedule. The Linear Sprint Group performed maximal 40-meter linear sprints, whereas the Game-Based Sprint Group performed soccer-specific sprint activities that included running, ball involvement, and technical actions. The Control Group continued regular soccer training without an additional sprint-specific intervention.

Sprint performance, change-of-direction performance, and right and left hamstring strength were assessed at baseline, Week 6, and Week 12. Maximum running velocity was also monitored during official matches throughout the 12-week study period. The study was designed to compare how the two sprint training approaches affected performance over time and whether changes observed during standardized testing were also reflected in maximum running velocity during competitive matches.

Study Overview

Study Type

Interventional

Enrollment (Actual)

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 Locations

    • Istanbul
      • Istanbul, Istanbul, Turkey (Türkiye), 34310
        • İstanbul Gelisim University

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 amateur-licensed soccer players.
  • A minimum of 5 years of regular soccer training experience.
  • Participation in organized soccer training at least 5 days per week.

Exclusion Criteria:

  • A serious musculoskeletal injury within the previous 6 months that could interfere with participation in the training intervention or performance assessments.
  • Musculoskeletal surgery within the previous 6 months that could interfere with the study outcomes.

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Linear Sprint Group (LSG)
Participants performed maximal 40-m linear sprint training once weekly on M-3 (Wednesday), approximately 72 hours before the official match, in addition to their regular soccer training. The 12-week intervention was progressively structured across three four-week phases.
Participants performed maximal 40-m linear sprints once weekly for 12 weeks. During Weeks 1-4, participants completed 2 sets of 4 repetitions with 90 seconds of recovery between repetitions and 3 minutes between sets. During Weeks 5-8, they completed 3 sets of 4 repetitions with the same recovery periods. During Weeks 9-12, they completed 3 sets of 5 repetitions with 90 seconds of recovery between repetitions and 4 minutes between sets. The intervention was performed in addition to regular soccer training.
Experimental: Game-Based Sprint Group (GBSG)
Participants performed game-based sprint training once weekly on M-3 (Wednesday), approximately 72 hours before the official match, in addition to their regular soccer training. Training consisted of soccer-specific maximal sprint actions within a standardized crossing-and-shooting drill incorporating ball involvement, perceptual demands, and technical actions. The 12-week intervention was progressively structured across three four-week phases.
Participants performed soccer-specific maximal sprint actions within a standardized crossing-and-shooting drill once weekly for 12 weeks. During Weeks 1-4, participants completed 2 sets of 4 repetitions of 8-10-second contextual sprint actions, with 90 seconds of recovery between repetitions and 3 minutes between sets. During Weeks 5-8, they completed 3 sets of 4 repetitions using the same sprint duration and recovery periods. During Weeks 9-12, they completed 3 sets of 5 repetitions of 10-12-second contextual sprint actions, with 90 seconds of recovery between repetitions and 4 minutes between sets. The drills incorporated ball involvement, perceptual demands, and soccer-specific technical actions.
No Intervention: Control Group (CG)
Participants continued their regular competitive-season soccer training and match schedule throughout the 12-week study period without receiving any additional sprint-specific intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
40-m Sprint Performance
Time Frame: Baseline (Week 0), Week 6, and Week 12
The time required to complete a 40-m maximal linear sprint was measured using the SmartSpeed electronic timing system (VALD Performance, Australia). Participants completed two maximal trials, and the fastest time was retained for analysis. Lower values indicate better sprint performance.
Baseline (Week 0), Week 6, and Week 12

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
T-Drill Change-of-Direction Performance
Time Frame: Baseline (Week 0), Week 6, and Week 12
Change-of-direction performance was assessed using the T-drill test. Participants completed two maximal trials, and the fastest completion time was retained for analysis. Lower values indicate better performance.
Baseline (Week 0), Week 6, and Week 12
Hamstring Strength
Time Frame: Baseline (Week 0), Week 6, and Week 12
Bilateral hamstring strength was assessed using the NordBord system (VALD Performance). Right and left limbs were assessed separately, with force recorded in Newtons (N). Participants completed two maximal-effort trials for each limb, and the highest value was retained for analysis.
Baseline (Week 0), Week 6, and Week 12
Match Maximum Running Velocity
Time Frame: During official matches throughout the 12-week intervention period
Maximum running velocity during official soccer matches was monitored using the Catapult S7 GPS system. The highest running velocity achieved by each participant during each official match was retained for analysis.
During official matches throughout the 12-week intervention period

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)

November 1, 2025

Primary Completion (Actual)

January 24, 2026

Study Completion (Actual)

January 24, 2026

Study Registration Dates

First Submitted

August 28, 2026

First Submitted That Met QC Criteria

August 28, 2026

First Posted (Actual)

September 2, 2026

Study Record Updates

Last Update Posted (Actual)

September 2, 2026

Last Update Submitted That Met QC Criteria

August 28, 2026

Last Verified

August 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • SPRINT-RCT-2025-397267

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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