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Machine Learning-Guided Training for Elite Athletes (MLGT) (MLGT)

27. juni 2026 oppdatert av: Dr. Arefayne Mesfen Dessye, Debre Berhan University

A Machine Learning-Guided Training Approach to Reduce Injuries and Enhance Performance in Elite Athletes: A Prospective Cohort Evaluation

Plaintext The purpose of this study is to evaluate whether a personalized training protocol driven by machine learning can successfully reduce time-loss sports injuries and enhance athletic performance in elite athletes.

During a 9-month competitive sports season, a group of elite athletes was divided into two training

Studieoversikt

Detaljert beskrivelse

This study evaluated the efficacy of an adaptive, machine learning-driven training protocol compared to traditional athletic preparation over a full 9-month competitive sports season. The primary objective was to determine if a dynamic, technology-led approach to training load management could minimize time-loss injuries while concurrently optimizing athletic performance markers.

Participants were elite athletes randomly allocated into two parallel groups:

  1. The Experimental Group, which underwent training regimens dynamically adjusted using a machine learning algorithm that analyzed individual biomechanical data and historical workload parameters to optimize training volume and intensity.
  2. The Control Group, which followed standard, predetermined high-performance athletic training protocols typical for competitive season preparation.

Throughout the 9-month intervention period, daily tracking was maintained by technical and coaching staff. Data collection focused on the incidence, severity, and duration of all time-loss sports injuries. Concurrently, sport-specific performance parameters were periodically assessed to evaluate physical conditioning and competitive readiness. Statistical analyses were subsequently conducted to compare cumulative injury rates, total days lost to injury, and net performance adaptations between the two cohorts.

Studietype

Intervensjonell

Registrering (Faktiske)

120

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiesteder

    • Shewa
      • Debre Berhan, Shewa, Etiopia, 445
        • Dr. Arefayne
      • Debre Berhan, Shewa, Etiopia, 445
        • M Dessye

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:

  1. Must be a competitive, elite-level or sub-elite track and field athlete specializing in short-to-mid distance running events.
  2. Aged between 18 and 35 years old.
  3. Actively participating in structured athletic training programs for at least 2 years prior to enrollment.
  4. Free from any acute musculoskeletal injuries or medical conditions that prevent full participation in high-intensity training protocols.
  5. Capable and willing to provide written informed consent to participate in the study.

Exclusion Criteria: 1. Current or recent (within the past 3 months) major lower-limb injury or surgery that restricts maximal sprint or aerobic performance.

2. Concurrent use of performance-enhancing drugs or medications that influence metabolic or cardiovascular responses.

3. Inability to maintain consistent participation in the designated training protocols due to scheduling conflicts or travel.

4. Any underlying cardiovascular, respiratory, or systemic condition that creates a health risk during exhaustive exercise testing.

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

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

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Control Cohort
Elite adolescent sprinters who followed standard, predetermined high-performance athletic training protocols typical for competitive season preparation. This group received structured training volume and intensity matching standard athletic coaching guidelines, without any machine learning interventions or adaptive workload adjustments.
A personalized, data-driven training intervention where athletic workloads are dynamically adjusted based on predictive modeling. The protocol continuously tracks individual physiological markers, biomechanical data, and workload history to optimize training volume and intensity. This adaptive approach aims to maximize performance gains while minimizing the risk of overtraining and injury during the competitive season.
Eksperimentell: Algorithmic Cohort
Elite adolescent sprinters who received a personalized training protocol dynamically optimized by a machine learning algorithm. The framework evaluated individual biomechanical variables, morning heart rate variability (HRV), sleep quality, and physiological fatigue metrics to adjust training volume and intensity.
A personalized, data-driven training intervention where athletic workloads are dynamically adjusted based on predictive modeling. The protocol continuously tracks individual physiological markers, biomechanical data, and workload history to optimize training volume and intensity. This adaptive approach aims to maximize performance gains while minimizing the risk of overtraining and injury during the competitive season.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Changes in Sprint Performance Time
Tidsramme: 12 weeks
Sprint performance will be assessed using electronic timing gates to record running times over a specific distance from a stationary start. Lower times indicate improved sprint performance. Measurements will be taken at baseline and at the conclusion of the training intervention period to evaluate the impact of the workload protocols.
12 weeks

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Dr. Arefayne M Dessye, PhD, Debre Berhan Univeristy

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. januar 2023

Primær fullføring (Faktiske)

30. september 2023

Studiet fullført (Faktiske)

30. september 2023

Datoer for studieregistrering

Først innsendt

27. juni 2026

Først innsendt som oppfylte QC-kriteriene

27. juni 2026

Først lagt ut (Faktiske)

6. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

27. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • DBU-SS-2023-008
  • IRB#DBU-SS-2023-008 (Registeridentifikator: ClinicalTrials.gov)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

Individual participant data (IPD) will not be shared publicly to maintain the confidentiality of the elite athletes involved and to protect proprietary training protocols. Aggregated study results and statistical analyses will be available through academic publication.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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