Does the Structure of the Tendon Relate to the Temporal, Kinetic and Kinematic Jump Variables? Athletes Vs. Non Athletes

February 12, 2025 updated by: Daniela Ferreira Carneiro, Escola Superior de Tecnologia da Saúde do Porto

Does the Structure of the Tendon Relate to the Temporal, Kinetic and Kinematic Jump Variables? Athletes Vs. Non Athletes: an Observational Study

The goal of this observational study is to investigate the relationship between temporal, kinetic, and kinematic jump variables and patellar and Achilles tendons' structure in athletes and non-athletes. The main research questions are:

Does the structure of the patellar and Achilles tendons relate to the temporal, kinetic, and kinematic jump variables? Does the relationship between these variables differ between athletes and non-athletes? To answer these questions, researchers will compare the two groups to determine if the relationships between the variables are similar. Participants will undergo a UTC (Ultrasound Tissue Characterization) scan of the patellar and Achilles tendons and perform five jumps: a countermovement jump, a single-leg countermovement jump on each leg and a single-leg horizontal jump on each leg.

Study Overview

Status

Active, not recruiting

Study Type

Observational

Enrollment (Actual)

48

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Porto, Portugal, 4200-072
        • Escola Superior de Saúde do Instituto Politécnico do Porto

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The target population for this study consisted of young adults aged 18 to 35, of both sexes, including volleyball athletes and non-athletes.

Description

Inclusion Criteria for the Athletes Group:

  1. Being a volleyball athlete competing in the 1st or 2nd division of the portuguese national championship;
  2. Participating in training and games for more than 20 hours per week.

Exclusion Criteria for the Athletes Group:

  1. Presence of any musculoskeletal, neurological, cardiorespiratory, or metabolic condition that affects jumping performance;
  2. Absence from competition due to injury or illness in the last two weeks;
  3. History of tendon rupture;
  4. Previous tendon surgery;
  5. Diagnosis of patellar tendinopathy in the last 12 months.

Exclusion Criteria for the Non-Athletes Group:

  1. Presence of any musculoskeletal, neurological, cardiorespiratory, or metabolic condition that affects jumping performance;
  2. Absence from competition due to injury or illness in the last two weeks;
  3. History of tendon rupture;
  4. Previous tendon surgery;
  5. Diagnosis of patellar tendinopathy in the last 12 months;
  6. Previous participation in a jumping sport.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Athletes
The participants in the athlete group were volleyball players competing in the 1st or 2nd division of the Portuguese National Championship, training and/or competing for more than 20 hours per week.
Non Athletes
The participants in the non-athlete group had no prior experience in any jumping sport.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Tendon Structure
Time Frame: Baseline

Ultrasound Tissue Characterization (UTC) captures tendon structure and quantifies the number of altered fibers. This technology classifies tendon structure into four echo types, reflecting tendon integrity and fibrillar organization. Data collection for the patellar tendon will be conducted with participants seated, hips and knees at 90° flexion, and feet supported on a stable surface. For the Achilles tendon, the participants will be lying down with ankle in neutral position.

This positioning ensures the probe is aligned transversely to the tendons, enabling the acquisition of optimal ultrasound images without anisotropy.

Ultrasound parameters will be standardized for all scans: a 40-second B-mode ultrasound using a 7-10 Hz linear transducer, with the probe attached to a tracking device that moves automatically along the tendon's perpendicular axis, capturing consecutive images at 0.2 mm intervals. A single scan of the tendons will be performed for each knee.

Baseline
Jump Variables
Time Frame: Baseline

The data collection protocol includes the following tasks: countermovement jump, single-leg countermovement jump with the dominant leg, single-leg countermovement jump with the jumping leg, single-leg horizontal jump with the jumping leg and single-leg horizontal jump with the dominant leg. Kinematic variables will be analyzed by recording the spatial positions of reflective markers placed on specific anatomical regions. Data will be captured using the Qualisys Motion Capture System (version 2021.2).

Ground reaction forces will be measured using a force platform connected to a signal amplifier. The platform records the three components of ground reaction forces-anteroposterior, mediolateral, and vertical-via four sensors.

The image capture hardware is connected to the Qualisys USB Analog Acquisition interface, synchronizing temporal, kinetic, and kinematic data with the Qualisys Track Manager (QTM) software.

Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 5, 2024

Primary Completion (Estimated)

September 30, 2025

Study Completion (Estimated)

September 30, 2025

Study Registration Dates

First Submitted

December 10, 2024

First Submitted That Met QC Criteria

December 10, 2024

First Posted (Actual)

December 13, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 12, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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