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

28. august 2026 oppdatert av: 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.

Studieoversikt

Studietype

Intervensjonell

Registrering (Faktiske)

36

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Istanbul
      • Istanbul, Istanbul, Tyrkia (Türkiye), 34310
        • Istanbul Gelisim University

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Ja

Beskrivelse

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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
Eksperimentell: 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.
Ingen inngripen: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
40-m Sprint Performance
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
T-Drill Change-of-Direction Performance
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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

Samarbeidspartnere og etterforskere

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Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. november 2025

Primær fullføring (Faktiske)

24. januar 2026

Studiet fullført (Faktiske)

24. januar 2026

Datoer for studieregistrering

Først innsendt

28. august 2026

Først innsendt som oppfylte QC-kriteriene

28. august 2026

Først lagt ut (Faktiske)

2. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

2. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

28. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • SPRINT-RCT-2025-397267

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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