- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06829056
Presence of Pain Shows Greater Effect Than Tendon Structural Alignment During Landing Dynamics
The goal of this observational study is to investigate the relationship between temporal, kinetic, and kinematic jump variables and patellar tendons' structure in athletes. The main research questions are:
Does the structure of the patellar tendon relate to the temporal, kinetic, and kinematic variables of different jumps?
To answer these questions, participants will undergo a UTC (Ultrasound Tissue Characterization) scan of the patellar tendon and perform two vertical jump: a countermovement jump and tuck jump test.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Porto, Portugal, 4200-072
- Escola Superior de Saúde do Instituto Politécnico do Porto
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- aged between 18-30 years;
- competing in the highest-level Portuguese volleyball league with a minimum of 10 years of volleyball practice.
Exclusion Criteria:
- presence of injuries or discomfort that impeded maximal jumping tests;
- history of surgery within the last 12 months;
- illness during data collection
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Athletes
Included volunteer participants were aged between 18-30 years, competing in the highest-level Portuguese volleyball league with a minimum of 10 years of volleyball practice.
Participants were excluded in presence of injuries or discomfort that impeded maxi- mal jumping tests, history of surgery within the last 12 months or illness during data collection.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Tendon Structure
Time Frame: Baseline
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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.
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Baseline
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Jump Variables
Time Frame: baseline
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The data collection protocol includes the following tasks: countermovement jump and tuck jump test.
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.
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baseline
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Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- FIS-2022-06
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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