Musculotendinous Adaptations in High and Low- Performance Triathletes

NCT ID: NCT06318728

Last Updated: 2024-03-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-04-01

Study Completion Date

2024-10-04

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study aims to investigate the musculotendinous adaptations in the Achilles tendon and the muscles composing the triceps surae induced by triathlon training and competitions in high-performance and low-performance athletes. Twenty high-performance triathletes, twenty low-performance triathletes, and twenty physically active and healthy individuals of both genders will be recruited to constitute the research groups. Ultrasonography will be employed as the assessment method for the structures of the Achilles tendon and the muscular architecture of the triceps surae. The quality and portability of ultrasonography, coupled with its real-time information capabilities, make it the appropriate choice for this evaluation. The VISA-A scale (Victorian Institute of Sport Achilles Assessment) will be used to measure pain and function of the Achilles tendon. The reliability of ultrasonography measures will be obtained by evaluating images of individuals using the intraclass correlation coefficient, allowing for the analysis of result reproducibility. Data analysis will involve comparisons among the high-performance, low-performance, and physically active groups, aiming to identify differences in musculotendinous adaptations related to performance and injury predisposition. Structural changes occurring in these structures and their potential association with sports performance and/or injury predisposition will be explored. Overall, this study utilizes a comparative cross-sectional research design, where different groups are assessed regarding musculotendinous adaptations in the Achilles tendon and triceps surae through ultrasound-derived measures. The use of the VISA-A scale and the assessment of measure reliability will provide additional data on pain, function, and result reproducibility.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Introduction: Triathlon is a growing sport worldwide, accompanied by a range of injuries primarily linked to the running component, with calcaneal tendinopathy standing out prominently due to the significant demands placed on this structure in both running and cycling. While numerous studies have assessed the architecture of triceps surae muscles and the Achilles tendon in athletes from various sports, exploring both positive and negative adaptations, as well as characteristics associated with improved performance or injury predisposition, there is a notable absence of research specifically investigating these tissues in triathletes. Understanding the architecture of the Achilles tendon and triceps surae muscles in this specific population is crucial for elucidating structural alterations related to performance and injurious changes in these structures. Ultrasound imaging emerges as the standard examination for evaluating these structures due to its quality, portability, and real-time information provision.

Objective: This study aims to identify musculotendinous adaptations in the Achilles tendon and muscles composing the triceps surae induced by triathlon training and competitions in both high-performance and low-performance athletes. These adaptations may be related to injury predisposition and could explain differences in sports performance between groups.

Methods: Twenty high-performance triathletes, twenty low-performance triathletes, and twenty physically active, healthy individuals of both genders will be screened through anamnesis to determine the research groups. Pain and function of the Achilles tendon will be measured using the VISA-A scale (Victorian Institute of Sport Achilles Assessment). The structure of the Achilles tendon and the muscular architecture of the triceps surae will be assessed through ultrasound imaging. The reliability of ultrasound measures will be determined by evaluating images of individuals using the intraclass correlation coefficient.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Athletes

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

High Performance Triathletes Groups

Triathletes who have been practicing the sport for more than 2 years, can maintain a running pace in triathlon competition below 4 minutes and 10 seconds per kilometer for men and 4 minutes and 30 seconds per kilometer for women, and have a weekly running volume exceeding 35 kilometers.

No interventions assigned to this group

Low Performance Triathletes Groups

Triathletes who have completed at least 2 races, maintain a running pace in triathlon competition above 4 minutes and 50 seconds per kilometer for men and 5 minutes and 10 seconds per kilometer for women, and have a weekly running volume below 30 kilometers.

No interventions assigned to this group

Control Group

Physically active individuals, aged between 17 and 52 years, who do not engage in regular running.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

High and Low-Performance Triathlete Groups:

* Be a triathlete practicing the sport for more than one year.
* Have participated in and completed at least two triathlon events.
* Maintain regular training at least 4 times per week.
* Be between 17 and 52 years old.

Control Group:

* Be between 17 and 52 years old.
* Engage in regular physical activity (minimum 3 times per week).

Exclusion Criteria

High and Low-Performance Triathlete Groups:

* Have any disease or injury limiting training and competitions at the time of assessment.
* Not have been training regularly in the last 2 weeks prior to assessment.
* Present acute inflammation, acute pain, or delayed onset muscle soreness on the assessment day.
* Use anabolic steroids.
* Have used steroidal anti-inflammatories in the last 4 weeks before assessment.
* Have used Fluoroquinolone antibiotics in the last 4 weeks before assessment, as they may alter collagen synthesis and induce tendinopathies (ALVES; MENDES; MARQUES, 2019).
* Engage in regular practice of another sport.

Control Group:

* Have any disease or injury limiting physical activity.
* Regularly engage in street running (run at least 20km per week).
* Present acute inflammation, acute pain, or delayed onset muscle soreness on the assessment day.
* Use anabolic steroids.
* Have used steroidal anti-inflammatories in the last 4 weeks before assessment.
* Have used Fluoroquinolone antibiotics in the last 6 months before assessment, as they may alter collagen synthesis and induce tendinopathies (ALVES; MENDES; MARQUES, 2019).
* Have regularly practiced street running at any point in life.
Minimum Eligible Age

17 Years

Maximum Eligible Age

52 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Brasilia

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

João LQ Durigan, PhD

Role: STUDY_DIRECTOR

UnB

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Estevão s Diniz, Postgraduate

Role: CONTACT

62982089638 ext. +55

Rita CM Durigan, PhD

Role: CONTACT

62983432063 ext. +55

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CAEE - 70162723.0.0000.8093

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Immediate and Short-term Effects of Low-level Laser
NCT05344183 ACTIVE_NOT_RECRUITING NA