- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06111144
Effects of Polarized and Pyramidal Training Combined With or Without Mindfulness in Amateur Runners
Effects of Polarized and Pyramidal Training Models Combined With or Without Mindfulness on Running Time, Performance Variables, and Body Composition in Amateur Long-distance Runners. A Randomized Controlled Trial
Road running in athletics has grown worldwide in recent years, which has led to an increase in the number of recreational runners. Despite this growth, research addressing this population is scarce, with major limitations and methodological weaknesses. Two of the topics of recent interest in runners are the effects of training intensity distribution (TID) and mental training using mindfulness on running time, body composition and physiological parameters related to performance in endurance sports; the maximal oxygen consumption (VO2max), maximal aerobic speed (MAS) and ventilatory thresholds (VT).
The scarce evidence found identifies the TID polarized model as the most effective in sports performance and TID pyramidal model as the most used by elite runners. For mindfulness, it is identified as an emerging program that could contribute to performance in endurance sports.
Study Overview
Status
Conditions
Intervention / Treatment
- Behavioral: Polarized training intensity distribution (TID) without mindfulness
- Behavioral: Pyramidal training intensity distribution (TID) without mindfulness
- Behavioral: Polarized training intensity distribution (TID) and mental training using mindfulness
- Behavioral: Pyramidal training intensity distribution (TID) and mental training using mindfulness
Detailed Description
40 recreational long-distance runners will be randomly assigned into one of the following 4 TID models groups: polarized TID model group with mindfulness program (POL+), polarized TID model group without mindfulness program (POL-), pyramidal TID model group with mindfulness program (PYR+) and pyramidal TID model group without mindfulness program (PYR-). Each group will be composed of 10 subjects. The interventions will have a duration of 12 weeks.
All participants will have evaluation of 10 km running time, body composition and physiological parameters (VO2max, MAS and VT's 1 and 2) at week 0 and 13 of the study.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Cundinamarca
-
Bogotá, Cundinamarca, Colombia
- JC Running
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Amateur long-distance runners
- Running time of 10 km in Bogotá, Colombia or similar altitude (2600 m above sea level) for men between 45 and 60 minutes, and for women between 50 and 65 minutes.
Exclusion Criteria:
- Smokers.
- History of cardiovascular disease.
- Arrhythmias.
- Cardiac insufficiencies.
- Hypertension.
- Musculoskeletal problems that affect their participation in the training program.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Polarized training Intensity distribution model without mindfulness program
The TID of the entire training program will be zone 1 (80%), zone 2 (5%), zone 3 (15%). The periodization of the training will be performed in a 3:1 load-recovery cycle, that is, three weeks of load for one week of recovery, this cycle will be repeated 3 times to complete the 12 weeks. The running sessions will have a volume in the load weeks as follows: The first week a volume of 5 hours, the second week 5.5 hours and the third week 6 hours. In the recovery week the volume will be 4 hours. As for the running technique and strength, these will have a weekly volume of 30 min and 1 hour respectively during all 12 weeks. In summary: 60 running sessions 24 strength sessions 24 running technique sessions |
Polarized TID model group without mindfulness program (POL-)
|
Experimental: Pyramidal training Intensity distribution model without mindfulness program
The TID of the entire training program will be zone 1 (80%), zone 2 (5%), zone 3 (15%). The periodization of the training will be performed in a 3:1 load-recovery cycle, that is, three weeks of load for one week of recovery, this cycle will be repeated 3 times to complete the 12 weeks. The running sessions will have a volume in the load weeks as follows: The first week a volume of 5 hours, the second week 5.5 hours and the third week 6 hours. In the recovery week the volume will be 4 hours. As for the running technique and strength, these will have a weekly volume of 30 min and 1 hour respectively during all 12 weeks. In summary: 60 running sessions 24 strength sessions 24 running technique sessions |
Pyramidal TID model group without mindfulness program (PYR-).
|
Experimental: Polarized training Intensity distribution model with mindfulness program
The TID of the entire training program will be zone 1 (80%), zone 2 (5%), zone 3 (15%). The periodization of the training will be performed in a 3:1 load-recovery cycle, that is, three weeks of load for one week of recovery, this cycle will be repeated 3 times to complete the 12 weeks. The running sessions will have a volume in the load weeks as follows: The first week a volume of 5 hours, the second week 5.5 hours and the third week 6 hours. In the recovery week the volume will be 4 hours. As for the running technique, strength and mindfulness these will have a weekly volume of 30 min, 1 hour and 65 min respectively during all 12 weeks. The weekly mindfulness practice will be done in 4 different types of sessions: (life-meditation, jogging-meditation, stretching-meditation, running-meditation). In summary: 60 running sessions 60 mindfulness sessions 24 strength sessions 24 running technique sessions |
Polarized TID model group with mindfulness program (POL+)
|
Experimental: Pyramidal training Intensity distribution model with mindfulness program
The TID of the entire training program will be zone 1 (80%), zone 2 (15%), zone 3 (5%). The periodization of the training will be performed in a 3:1 load-recovery cycle, that is, three weeks of load for one week of recovery, this cycle will be repeated 3 times to complete the 12 weeks. The running sessions will have a volume in the load weeks as follows: The first week a volume of 5 hours, the second week 5.5 hours and the third week 6 hours. In the recovery week the volume will be 4 hours. As for the running technique, strength and mindfulness these will have a weekly volume of 30 min, 1 hour and 65 min respectively during all 12 weeks. The weekly mindfulness practice will be done in 4 different types of sessions: (life-meditation, jogging-meditation, stretching-meditation, running-meditation). In summary: 60 running sessions 60 mindfulness sessions 24 strength sessions 24 running technique sessions |
Pyramidal TID model group with mindfulness program (PYR+)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in 10 km race time
Time Frame: Week 0 and 13
|
The time in the 10 km will be taken by two evaluators with independent stopwatches, and the average of them will be taken as the official time.
The test will take place in a 1257 m loop, with a positive difference in altitude of 5 m.
|
Week 0 and 13
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in VO2max
Time Frame: Week 0 and 13
|
Incremental test to exhaustion on a Woodway© model 4Front treadmill. During the test, VO2 will be measured breath-by-breath by a portable metabolic system COSMED© model K5. The VO2max will be calculated as the average oxygen consumption of the last 30 seconds measured in the incremental test. |
Week 0 and 13
|
Change in ventilatory threshold 1
Time Frame: Week 0 and 13
|
Incremental test to exhaustion on a Woodway© model 4Front treadmill. During the test, ventilatory threshold 1 will be measured by a portable metabolic system COSMED© model K5. Ventilatory threshold 1 will be defined as the first increase in ventilatory equivalent for oxygen (VE/VO2) vs. load, without a simultaneous increase in ventilatory equivalent for carbon dioxide (VE/VCO2) vs. load. |
Week 0 and 13
|
Change in ventilatory threshold 2
Time Frame: Week 0 and 13
|
Incremental test to exhaustion on a Woodway© model 4Front treadmill. During the test, ventilatory threshold 2 will be measured by a portable metabolic system COSMED© model K5. Ventilatory threshold 2 will be defined as the second increase in ventilation with a concomitant rapid increase in VE/VO2 and VE/VCO2 and a decrease in the partial pressure of exhaled carbon dioxide (PETCO2). |
Week 0 and 13
|
Change in maximal aerobic speed
Time Frame: Week 0 and 13
|
Incremental test to exhaustion on a Woodway© model 4Front treadmill. During the test, maximal aerobic speed will be measured by a portable metabolic system COSMED© model K5. The maximal aerobic speed will be determined at the speed corresponding to the VO2max. |
Week 0 and 13
|
Change in body weight
Time Frame: Week 0 and 13
|
Body weight (kg) will be obtained using a HBF-514C OMRON© body composition analyzer
|
Week 0 and 13
|
Change in body fat
Time Frame: Week 0 and 13
|
Body fat (%) will be obtained using a HBF-514C OMRON© body composition analyzer
|
Week 0 and 13
|
Change in muscle mass
Time Frame: Week 0 and 13
|
Muscle mass (%) will be obtained using a HBF-514C OMRON© body composition analyzer
|
Week 0 and 13
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Keywords
Other Study ID Numbers
- TID-Runners-UdeA-JCRunning
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
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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