- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02498873
Linear Running Periodization x Nonlinear (Running)
January 17, 2016 updated by: Alberto Souza de Sá Filho, Universidade Federal do Rio de Janeiro
Linear Running Periodization x Nonlinear: a Cross Effect of Five Months Controlled Running on VO2Max and Critical Power Performance
In a competitive scenario, trainers and coaches seek to improve the performance of their athletes organizing macrocycles (year), mesocycles (months), and microcycles (weeks) training aimed at a specific moment of a competition.
The organization variables, mainly the intensity of exercise in a training routine can stimulate important physiological pathways and uphold superior gains to VO2max, leading to a peak aerobic performance.
However, due to lack of evidence, and the difficulty of control on a large scale, the effects of the intensity organization over a mesocycle periodization are still poorly investigated.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The objective of this study is compare two intensity blocks organization a) linear progression intensity (LP) and b) randomized or not intensity linaer (NLP) over five months running training, and a crossover design between subjects, on gains in VO2max, peak velocity (Vpeak) and critical power (CP).
Furthermore, the relationship between the gains obtained with the training and the amount of exercise will be established.
In our case all dependent variables will increase after training, with no significant differences between the two strategies on dependent variables.
Study Type
Interventional
Enrollment (Actual)
35
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
All
Description
Inclusion Criteria:
- Minimum standards of physical activity proposed by the ACSM
- 18-45 years
- No metabolic or cardiovascular events
- No use ergogenic resources
Exclusion Criteria:
- Sedentary
- Diagnosis of cardiac, pulmonary or diabetes type I or II
- No injuries
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
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Linear Periodization
Linear Periodization Running (Crossover Design)
|
Non Linear Periodization Running
Other Names:
|
|
Active Comparator: Non Linear Periodization
Non Linear Periodization Running (Crossover Design)
|
Linear Intensity Periodization Running
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
VO2Max
Time Frame: 0 - 2 month; 1 month (wash out); 3 - 5 month
|
Observe the improvement of VO2max
|
0 - 2 month; 1 month (wash out); 3 - 5 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Critical Power
Time Frame: 0 - 2 month; 1 month (wash out); 3 - 5 month
|
Performance of Critical Power in Linear Periodization and Non Linear Periodization
|
0 - 2 month; 1 month (wash out); 3 - 5 month
|
|
Peak Velocity
Time Frame: 0 - 2 month; 1 month (wash out); 3 - 5 month
|
Performance of Vpeak in Progressive Effort Test
|
0 - 2 month; 1 month (wash out); 3 - 5 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Sérgio Machado, PhD, Universidade Federal do Rio de Janeiro
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
August 1, 2015
Primary Completion (Actual)
December 1, 2015
Study Completion (Actual)
January 1, 2016
Study Registration Dates
First Submitted
July 11, 2015
First Submitted That Met QC Criteria
July 14, 2015
First Posted (Estimate)
July 15, 2015
Study Record Updates
Last Update Posted (Estimate)
January 20, 2016
Last Update Submitted That Met QC Criteria
January 17, 2016
Last Verified
January 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- UNIVERSO-01
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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