- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05218512
WB-EMS Increase Energy Expenditure at Rest and During Uphill Walking Exercise
January 30, 2022 updated by: Jonatan Ruiz Ruiz, Universidad de Granada
Acute Effects of Whole-body Electromyostimulation on Energy Expenditure at Resting and During Uphill Walking in Healthy Young Men
Whole-body electrical stimulation (WB-EMS) has become increasingly popular as a tool to provide additional benefits compared to conventional exercise.
However, the effects of the different electrical parameters on energy expenditure (EE) and respiratory exchange ratio (RER) remain poorly understood.
This study aims to determine and compare the effects of different electrical frequencies applied with WB-EMS in EE and RER at supine resting and during uphill walking exercise
Study Overview
Detailed Description
Obesity is a critical public health problem worldwide since it is a risk factor for cardiovascular diseases and mortality.
Increased body weight and obesity are the results of an imbalance between energy intake and energy expenditure (EE).
Body weight regulation and obesity are highly influenced by different factors such as genetic, physiology, and socioeconomics.
It is well known that physical exercise is an effective strategy to increase EE, improve body composition, physical fitness, and cardiometabolic risk factors.
Unfortunately, the principal barriers to abstaining from exercise are time constraints, the risk of injuries, and the lack of enthusiasm observed during the exercise sessions.
In this context, whole-body electromyostimulation (WB-EMS) training is becoming increasingly popular worldwide as a potential and attractive alternative to traditional training methods to increase EE.
The present study aimed to determine and compare the effects of different electrical frequencies applied with WB-EMS in EE and RER at supine resting and during uphill walking exercise.
Study Type
Observational
Enrollment (Actual)
10
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Granada, Spain, 18011
- University of Granada
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-
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
14 years to 46 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
We chose recreationally active males without any disease.
Description
Inclusion Criteria:
- (i) no previous experience with WB-EMS training
- (ii) having a stable body weight (variation of <5 kg in body weight over the previous 3 months)
- (iii) normal weight (body mass index (BMI) between 18.5-25.0 kg/m2)
Exclusion Criteria:
- (i) Suffering from any health problem that might be aggravated by exercise or any contraindications for WB-EMS, such as total endoprosthesis, epilepsy and abdomen/groin hernia
- (ii) Taking medications
- (iii) Chronic metabolic disease or cancer
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
- Observational Models: Case-Only
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
WB-EMS
Young recreationally active males without any disease.
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The group has been submitted to 2 experimental conditions:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Energy expenditure
Time Frame: It will be continuously measured through the entire test (60 minutes) of electromyostimulation with different impulse frequencies and intensities.
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Change in energy expenditure (kcal/min) by indirect calorimetry (Vyntus CPX Metabolic Cart)
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It will be continuously measured through the entire test (60 minutes) of electromyostimulation with different impulse frequencies and intensities.
|
|
Resting exchange ratio
Time Frame: It will be continuously measured through the entire test (60 minutes) of electromyostimulation with different impulse frequencies and intensities.
|
Change in resting exchange ratio (kcal/min) by indirect calorimetry (Vyntus CPX Metabolic Cart)
|
It will be continuously measured through the entire test (60 minutes) of electromyostimulation with different impulse frequencies and intensities.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain perception
Time Frame: It will be measured at timepoints after the administration of each impulse frequency and before and after the whole application of electromyostimulation.
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Change in pain perception in different body structures by Visual Analogue Scales.
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It will be measured at timepoints after the administration of each impulse frequency and before and after the whole application of electromyostimulation.
|
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Impulse intensities
Time Frame: It will be measured with at timepoints after the administration of each impulse frequency.
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Change in impulse intensities in different body structures by whole-body electromyostimulation device.
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It will be measured with at timepoints after the administration of each impulse frequency.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
October 1, 2018
Primary Completion (Actual)
November 30, 2018
Study Completion (Actual)
November 30, 2018
Study Registration Dates
First Submitted
December 14, 2021
First Submitted That Met QC Criteria
January 30, 2022
First Posted (Actual)
February 1, 2022
Study Record Updates
Last Update Posted (Actual)
February 1, 2022
Last Update Submitted That Met QC Criteria
January 30, 2022
Last Verified
January 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- Impulse frequencies at rest
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
IPD Plan Description
Results will be shared with the scientific community.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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