- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02514330
Running Slopes and Power Performance
July 31, 2015 updated by: Alberto Souza de Sá Filho, Universidade Federal do Rio de Janeiro
Concurrent Effect of Running in Different Slopes on Power Performance
The objective of the present study was to determine the effect of interval session running at high intensity with 1% or 10% gradient on the height of the drop jump.
The cinematic variables concentric phase, eccentric and contact time were compared after the running session in both conditions in order to explain possible changes in the jump performance.
The investigators theorize that the lower eccentric overload in the running to 10% inclination promotes higher deleterious effect on power performance of the lower limbs
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Physical training programs are typically composed of activities directed to the development of different valences usually stimulated in the same session.
When aerobic activities of long duration prior isokinetic strength exercises, isotonic, or explosive, deleterious effects seem to be induced on performance of these valences.
These short and long-term changes in muscle strength and power would be directly associated with repetitive eccentric loads that characterize the endurance running.
Gradual increases in the running slope were inversely associated with a proportional reduction in the eccentric loads, which in turn would result in less muscle damage to intra and extrafusal fibers.
So, the change in the slope of the race would emerge as an optional way to neutralize the competitive effect on the power performance.
The research consisted of five visits.
At the initial visit was conducted familiarization to vertical drop jump, and immediately after, the determination of VO2max values and their associated speed (vVO2max).
The second visit was a new familiarization for the vertical drop jump followed immediately determining the Time to exhaustion performance in vVO2max (100% of VO2Max).
Two jumps were performed on each of the three selected heights (20, 30 and 40 cm) were used in the experimental sessions and control only the height associated with the highest performance.
In subsequent visits (third to fifth), participants performed three maximum jumps before and about 10 min after the following conditions: high intensity Interval running a 10% gradient (C10%), 1% grade (C1%) and control condition (CON).
Study Type
Interventional
Enrollment (Actual)
25
Phase
- Not Applicable
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
18 years to 45 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- age: 18 at 45 years
- no cardiovascular or metabolic problems
- minimum level of aerobic activity recommended by American College of Sports Medicine
Exclusion Criteria:
- no joint or muscle injuries
- no use ergogenic or anabolic resources
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
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Interval Training at 1% incline
Procedure: Initial Drop Jump (20;30;40 cm), Six Stimulus of High Intensity Interval Training at 1% incline, Final Drop Jump (20;30;40 cm)
|
Six stimuli were performed to exhaustion.
The vertical drop jump strategy (height and kinematics) served to establish the magnitude of the concurrent effect
Other Names:
|
Experimental: Interval Training at 10% incline
Procedure: Initial Drop Jump (20;30;40 cm), Six Stimulus of High Intensity Interval Training at 10% incline, Final Drop Jump (20;30;40 cm)
|
Six stimuli were performed to exhaustion.
The vertical drop jump strategy (height and kinematics) served to establish the magnitude of the concurrent effect.
Other Names:
|
No Intervention: Control
Procedure: Initial Drop Jump (20;30;40 cm), 20 min Rest, Final Drop Jump (20;30;40 cm)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Kinematic of Height Jump
Time Frame: up to 1 month
|
the same group (N=25) of subjects performed the experimental procedure in the last three sessions aiming to achieve the highest performance in all three conditions
|
up to 1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Kinematic of Concentric Phase
Time Frame: up to 1 month
|
the same group of subjects performed the experimental procedure in the last three sessions
|
up to 1 month
|
Kinematic of Excentric Phase
Time Frame: up to 1 month
|
the same group of subjects performed the experimental procedure in the last three sessions
|
up to 1 month
|
Kinematic of Contact Time
Time Frame: up to 1 month
|
the same group of subjects performed the experimental procedure in the last three sessions
|
up to 1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Tony Santos, Doctor, Universidade Federal de Pernambuco
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
March 1, 2012
Primary Completion (Actual)
August 1, 2012
Study Completion (Actual)
December 1, 2012
Study Registration Dates
First Submitted
July 29, 2015
First Submitted That Met QC Criteria
July 31, 2015
First Posted (Estimate)
August 3, 2015
Study Record Updates
Last Update Posted (Estimate)
August 3, 2015
Last Update Submitted That Met QC Criteria
July 31, 2015
Last Verified
July 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UGF 02
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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