- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02481063
Adaptation in Lower Extremity After 3 Running Days, With a Group Trained by Eccentric Overload
Differences in Muscle (Vastus Laterals and Gastrocnemius Medialis) and Tendon Adaptation (Patellar and Achilles) in Lower Extremity After 3 Running Days With a Group Trained by Eccentric Overload, Measured by Ultrasound and Thermography
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Changes in muscle and tendon tissues, due to exercise, could determine in the future the possibility of an injury. Understand the changes in the mechanical tissues is a key tool for prevention.
The evaluation of the thickness and area in tendons, the existence of new vessels within the tendon, muscle pennation angle or thermography are tools that have been widely used to detect these changes.
Running is one of the activities that can cause more muscle-tendon injuries, specially overuse injuries. However, the eccentric exercise suggest to make some adaptations in different tissues that may be beneficial to prevent damage after exercise.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Zaragoza
-
Villanueva de Gallego, Zaragoza, Spain, 50830
- Universidad San Jorge
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy subjects that performs any sport usually
- Subjects that never have made eccentric training will be included.
- Subjects must be willing to perform the procedure
- Sign informed consent
Exclusion Criteria:
- Subjects enrolled with lower limb pathology in last 6 months
- Subjects that don´t complete all the procedure will be excluded.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Eccentric
6 Weeks Training with eccentric Overload (Squat with Yoyo Technology) 3 Consecutive Days Running 1 hour at 80% of Maximus Heart Rate
|
3 Consecutive Days Running at 80% Maximus Heart Rate
Training with Eccentric Overload (Squat in Yoyo Technology) during 6 Weeks 3 Consecutive Days Running at 80% Maximus Heart Rate
|
|
Active Comparator: Control
3 Consecutive Days Running 1 hour at 80% of Maximus Heart Rate
|
3 Consecutive Days Running at 80% Maximus Heart Rate
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Composite Measure with Ultrasound in Tendons and Muscles
Time Frame: Change from Baseline in tendon structure, an expected average of 3 days of running
|
Ultrasound in Patellar and Achilles Tendon, to measure area, thickness and new blood vessels with Doppler. Ultrasound in Vastus Lateralis and Gastrocnemius Medialis to measure pennation angle |
Change from Baseline in tendon structure, an expected average of 3 days of running
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Temperature changes in Patellar and Achilles Tendon as assessed by thermography
Time Frame: Change from Baseline in tendon structure after 3 days of running. Just immediately and 10 minutes after intervention
|
Thermography in Patellar and Achilles Tendon in order to measure changes in temperature os these areas of interest
|
Change from Baseline in tendon structure after 3 days of running. Just immediately and 10 minutes after intervention
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: César Berzosa, Ph.D, Universidad San Jorge
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- TF_US20015
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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