Analysis of Injury Risk Factors in Elite Athletes
1 other identifier
observational
81
1 country
1
Brief Summary
Background information. The different disciplines of athletics place high physical demands on athletes. These different categories of running vary in terms of physical effort and duration, generating different levels of risk of injury. The description of the main injuries that affect elite athletes in the different athletics disciplines, as well as the identification of the specific risk factors of each discipline, will allow the identification of preventive measures to be implemented. Objective. To identify the risk factors for tendon injury in professional long- and middle-distance athletes, according to the type of event, and to identify the best predictive model for tendon injuries based on anthropometric and athletic variables. Method. Ambispective cohort study. 81 elite athletes will be recruited. The primary variable will be the number of tendon injuries in the last three seasons. The secondary and modifying variables will be: age (in completed years), weekly training load (in minutes), type of footwear (sneakers without carbon plate, sneakers with carbon plate, spiked sneakers without carbon plate and spiked sneakers with carbon plate), diet (balanced, high in carbohydrates, high-protein, controlled hypocaloric and adapted to the training cycle) and the regular practice of another physical activity. The possible confounding variables will be the body mass index, the date of tendon injuries in that period and the time spent as a federated athlete (in completed months). The analysis will calculate the risk of injury in these athletes and assess the influence of confounding factors and trend analysis on the primary variable, stratified by possible confounding factors. Expected results. To calculate the risk of injury in elite athletes based on anthropometric and sociodemographic variables. To identify the predictive model of tendon injuries in elite athletes
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Mar 2025
Shorter than P25 for all trials
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 25, 2025
CompletedStudy Start
First participant enrolled
March 31, 2025
CompletedFirst Posted
Study publicly available on registry
April 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 28, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2025
CompletedFebruary 10, 2026
March 1, 2025
28 days
March 25, 2025
February 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Measurement of number of lower limb tendon injuries
The primary variable will be the number of lower limb tendon injuries in the last three seasons
Screening visit
Secondary Outcomes (5)
Measurement of age
Screening visit
Measurement of the weekly training load
Screening visit
Measurement of the type of footwear
Screening visit
Measurement of the type of diet
Screening visit
Measurement of the practice of another physical activity
Screening visit
Other Outcomes (3)
Measurement of the body mass index
Screening visit
Measurement of the date of tendon injuries
Screening visit
Measurement of federated time
Screening visit
Study Arms (1)
Observacional group
Interventions
Elite athletes in whom the risk of injury will be calculated and the influence of confounding factors will be assessed through a personal interview.
Eligibility Criteria
Elite athletes
You may qualify if:
- Elite federated athletes
- Who have not undergone previous musculoskeletal surgery in the seasons under study
- Who were federated at least one year before the study period
- Sign the informed consent document.
You may not qualify if:
- Athletes who have not participated in competition, during the study seasons, for a period of more than 6 months due to a musculoskeletal injury
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Oviedo
Oviedo, Principality of Asturias, 33006, Spain
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Rubén Cuesta-Barriuso
Universidad de Oviedo
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 25, 2025
First Posted
April 2, 2025
Study Start
March 31, 2025
Primary Completion
April 28, 2025
Study Completion
May 15, 2025
Last Updated
February 10, 2026
Record last verified: 2025-03