Game-Based Versus Linear Sprint Training in Male Soccer Players
GBS-LST
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
1 other identifier
interventional
36
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2025
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
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 24, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 24, 2026
CompletedFirst Submitted
Initial submission to the registry
August 28, 2026
CompletedFirst Posted
Study publicly available on registry
September 2, 2026
CompletedSeptember 2, 2026
August 1, 2026
3 months
August 28, 2026
August 28, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
40-m Sprint Performance
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 Outcomes (3)
T-Drill Change-of-Direction Performance
Baseline (Week 0), Week 6, and Week 12
Hamstring Strength
Baseline (Week 0), Week 6, and Week 12
Match Maximum Running Velocity
During official matches throughout the 12-week intervention period
Study Arms (3)
Linear Sprint Group (LSG)
EXPERIMENTALParticipants 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.
Game-Based Sprint Group (GBSG)
EXPERIMENTALParticipants 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.
Control Group (CG)
NO INTERVENTIONParticipants continued their regular competitive-season soccer training and match schedule throughout the 12-week study period without receiving any additional sprint-specific intervention.
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul Gelisim University
Istanbul, Istanbul, 34310, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director
Study Record Dates
First Submitted
August 28, 2026
First Posted
September 2, 2026
Study Start
November 1, 2025
Primary Completion
January 24, 2026
Study Completion
January 24, 2026
Last Updated
September 2, 2026
Record last verified: 2026-08