- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03425981
Effects of WB-EMS in Runners.
EFFECTS OF WHOLE-BODY ELECTROMYOSTIMULATION TRAINING ON HEALTH AND PERFORMANCE PARAMETERS IN RECREATIONAL RUNNERS.
The subjects will be randomly distributed into 3 experimental groups: training with basic global electrostimulation (WB-EMS-SRT), training with specific global electrostimulation for runners (WB-EMS-WT) and control group (CG).
Initially and at the end of the intervention period, which will consist of six weeks, the subjects will undergo a series of tests: (1) Maximum incremental effort test in tapestry to exhaustion to determine cardiorespiratory capacity (VO2max) and thresholds (aerobic and anaerobic). (2) Submaximal carpet test at constant speed to determine race economy (EC). (3) Lower train power test (CMJ and Abalakov). (4) Weight, size and waist circumference. The aforementioned tests will be carried out on different days to avoid the effect of fatigue on performance with a break of more than 48 hours between tests.
The participants in the control group will maintain the volume and intensity of the training prior to the intervention study and the subjects of the WB-EMS and WB-EMS-AC groups will substitute one conventional training day for one with global electrostimulation for six weeks; the training of the first group will be non-specific and that of the second specific for runners and the duration of both will be 20 minutes.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Granada, Spain, 18001
- Medicine Faculty
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Frequent runners
Exclusion Criteria:
- Received WB-EMS training.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: WB-EMS-SRT
Training with basic global electrostimulation
|
The WB-EMS training program consisted of six WB-EMS training sessions (one per week) and six running training sessions (also one per week). This intervention programme followed a within-day undulating periodization model. The training sessions were divided into four parts: warm up (A), strength (B), high intensity interval power training (c), and high intensity interval training (HIIT) (D). |
|
Experimental: WB-EMS-WT
Training with specific global electrostimulation for runners
|
The WB-EMS training program consisted of six WB-EMS training sessions (one per week) and six running training sessions (also one per week). This intervention programme followed a within-day undulating periodization model. The training sessions were divided into four parts: warm up (A), strength (B), high intensity interval power training (c), and high intensity interval training (HIIT) (D). |
|
Placebo Comparator: CG
The participants in the control group will maintain the volume and intensity of the training prior to the intervention study and the subjects of the WB-EMS and WB-EMS-AC groups will substitute one conventional training day for one with global electrostimulation for six weeks; the training of the first group will be non-specific and that of the second specific for runners and the duration of both will be 20 minutes.
|
The WB-EMS training program consisted of six WB-EMS training sessions (one per week) and six running training sessions (also one per week). This intervention programme followed a within-day undulating periodization model. The training sessions were divided into four parts: warm up (A), strength (B), high intensity interval power training (c), and high intensity interval training (HIIT) (D). |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximal oxygen consumption
Time Frame: Baseline and through study completion, an average of 5 weeks
|
Maximal Oxygen consumption was assessed using a maximum treadmill (H/P/ Cosmos Pulsar treadmill, H/P/Cosmos Sport & Medical GMBH, Germany) exercise test with a progressive incremental protocol that has been used.
|
Baseline and through study completion, an average of 5 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ventilatory thresholds
Time Frame: Baseline and through study completion, an average of 5 weeks
|
VT1 and VT2 were estimated from gas exchange data through different respiratory variables: minute ventilation (VE) and equivalents for oxygen (VE/VO2) and carbon dioxide (VE/VCO2) by two independent researchers
|
Baseline and through study completion, an average of 5 weeks
|
|
Running economy
Time Frame: Baseline and through study completion, an average of 5 weeks
|
RE was determined during a treadmill test following a specific protocol used in previous studies
|
Baseline and through study completion, an average of 5 weeks
|
|
Muscular power
Time Frame: Baseline and through study completion, an average of 5 weeks
|
Vertical jump performance was assessed using the Bosco Test.
|
Baseline and through study completion, an average of 5 weeks
|
|
Weight
Time Frame: Baseline and through study completion, an average of 5 weeks
|
Weight in Kilograms
|
Baseline and through study completion, an average of 5 weeks
|
|
Body composition
Time Frame: Baseline and through study completion, an average of 5 weeks
|
Assessed using DXA.
|
Baseline and through study completion, an average of 5 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Baseline and post Castillo Garzón, University Proffesor, Universidad de Granada
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
Keywords
Other Study ID Numbers
- 200/CEIH/2016
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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