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The PERT Study - Training Factors of PERformance and Injuries (PERT)

5 november 2026 uppdaterad av: University Hospital, Clermont-Ferrand

The goal of this observational study was to learn about injuries in professional football players and to find out whether daily monitoring data could help predict injuries. The study followed male players from the first team and the reserve team of a French first-division professional football club over one full competitive season.

The main questions were:

How often did injuries occur among players over the season? Which day-to-day changes in routinely monitored data were linked to the onset of a new injury (all injuries combined, intrinsic and extrinsic)? Were the results similar when looking only at intrinsic injuries?

Each day, the club's staff recorded each player's physical workload during training sessions and matches using tracking technology. Players also reported how they felt, including sleep, fatigue, mood, and pain. New injuries were recorded daily by the club's medical staff. Players took part through the club's usual daily monitoring, with no additional tests or visits.

Studieöversikt

Status

Avslutad

Intervention / Behandling

Studietyp

Observationell

Inskrivning (Faktisk)

77

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Clermont-Ferrand, Frankrike
        • CHU de Clermont-Ferrand

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Barn
  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Manlig

Testmetod

Icke-sannolikhetsprov

Studera befolkning

Male football players from the first team and the reserve team of a French first-division professional football club, followed over one full competitive season.

Beskrivning

Inclusion Criteria:

  • Male football players belonging to the first team or the reserve team of the participating French first-division professional football club during the study season

Exclusion Criteria:

  • Fewer than 20 days of available monitoring data during the season

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Observationsmodeller: COHORT
  • Tidsperspektiv: RETROSPECTIVE

Kohorter och interventioner

Grupp / Kohort
Intervention / Behandling
Professional football players

Male players from the first team and the reserve team of a French first-division professional football club, followed daily over one full competitive season through the club's routine monitoring of external workload, self-reported wellness and injury status.

No intervention was assigned. Data came from the club's usual daily monitoring: external workload measured by tracking technology during training sessions and matches, and self-reported sleep, fatigue, mood, pain and perceived intensity.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Injury prevalence and occurrence of new injuries
Tidsram: Daily from June 26, 2023, to May 19, 2024 (47 weeks).

Daily injury status (non-injured or injured) recorded by the club's medical staff, used to describe season-long injury prevalence.

Daily from June 26, 2023, to May 19, 2024 (47 weeks).
Player characteristics
Tidsram: Daily from June 26, 2023, to May 19, 2024 (47 weeks).

Age (years), professional status (reserve team or professional), playing position (defender, midfielder or forward) and number of previous injuries (0, 1 or ≥2), examined as putative factors associated with injury occurrence.

Daily from June 26, 2023, to May 19, 2024 (47 weeks).
External workload
Tidsram: Daily from June 26, 2023, to May 19, 2024 (47 weeks).

Measured by tracking technology during training sessions and matches: match exposure (yes or no), session duration (minutes), total distance covered (km), number of accelerations and decelerations per day, distance covered (m) and number of sprints per day at 80-90% and 90-100% of each player's individual maximal speed. Examined as putative factors associated with injury occurrence.

Daily from June 26, 2023, to May 19, 2024 (47 weeks).
Self-reported wellness and perceived exertion
Tidsram: Daily from June 26, 2023, to May 19, 2024 (47 weeks).

Sleep time (hours/day), sleep quality (1 = best to 7 = worst), mood (1 = best to 7 = worst), fatigue (1 = min to 7 = max), pain (1 = min to 7 = max) and perceived exertion (1 = min to 10 = max). Examined as putative factors associated with injury occurrence.

Daily from June 26, 2023, to May 19, 2024 (47 weeks).

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Frédéric Dutheil, University Hospital, Clermont-Ferrand

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

1 juli 2024

Primärt slutförande (Faktisk)

30 maj 2025

Avslutad studie (Faktisk)

30 maj 2025

Studieregistreringsdatum

Först inskickad

2 november 2026

Först inskickad som uppfyllde QC-kriterierna

5 november 2026

Första postat (Faktisk)

9 november 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

9 november 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

5 november 2026

Senast verifierad

1 oktober 2026

Mer information

Termer relaterade till denna studie

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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