- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT07683091
Machine Learning-Guided Training for Elite Athletes (MLGT) (MLGT)
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
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
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:
- 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.
- 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
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
-
-
Shewa
-
Debre Berhan, Shewa, Ethiopië, 445
- Dr. Arefayne
-
Debre Berhan, Shewa, Ethiopië, 445
- M Dessye
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Must be a competitive, elite-level or sub-elite track and field athlete specializing in short-to-mid distance running events.
- Aged between 18 and 35 years old.
- Actively participating in structured athletic training programs for at least 2 years prior to enrollment.
- Free from any acute musculoskeletal injuries or medical conditions that prevent full participation in high-intensity training protocols.
- 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.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Actieve vergelijker: 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.
|
|
Experimenteel: 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.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Changes in Sprint Performance Time
Tijdsspanne: 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
|
Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Hoofdonderzoeker: Dr. Arefayne M Dessye, PhD, Debre Berhan Univeristy
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- DBU-SS-2023-008
- IRB#DBU-SS-2023-008 (Register-ID: ClinicalTrials.gov)
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .