- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05221203
Metabolic Cost of Bodyweight Training (BWT-UTH)
Study Overview
Status
Intervention / Treatment
Detailed Description
Bodyweight training has become a popular cardiovascular training choice in fitness centers and athletic performance enhancement facilities. Despite widespread use and growing popularity, little is known about the metabolic demands of such a training method. Therefore, the purpose of this study was to quantify the cardiovascular and metabolic cost from various foundational bodyweight exercises in order to contribute to a better planning of exercise programs in the real world.
Ten healthy young adults were assigned to execute seven bodyweight exercises (acute bout) for 30 and 45 seconds. Anthropometric, metabolic, and performance measurements were conducted at baseline. The metabolic cost was estimated from heart rate, blood lactate, resting oxygen uptake, exercise oxygen uptake, and excess post-exercise oxygen consumption measurements using a portable gas analyzer.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Trikala, Greece, 42100
- Laboratory of Exercise Physiology, Exercise Biochemistry and Sports Nutrition, School of Physical Education, Sports Sciences and Dietetics, University of Thessaly
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Aged between 18 and 35 years
- Physically active individuals
- Free of chronic diseases
- Free of musculoskeletal injuries
- Nonsmokers
Exclusion Criteria:
- Musculoskeletal injuries
- Chronic diseases
- Use of alcohol, caffeine and any type of ergogenic supplements or medication before (≤6 months) and throughout the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Training
Participants in this arm will perform seven bodyweight training exercises (acute bout per exercise) at two different conditions (30 and 45 seconds).
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Bodyweight training exercises will be performed for 30 seconds and the training volume will be consisted of 1 repetition.
Bodyweight training exercises will be performed for 45 seconds and the training volume will be consisted of 1 repetition.
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|
NO_INTERVENTION: Control
Participants in this arm will receive no intervention.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in exercise-induced energy expenditure
Time Frame: At pre-exercise, during, and post-exercise session (single bout lasting 30 and 45 seconds)
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Exercise energy expenditure (kcal) will be measured using a portable indirect calorimetry system
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At pre-exercise, during, and post-exercise session (single bout lasting 30 and 45 seconds)
|
|
Change in excess post-exercise oxygen consumption (EPOC)
Time Frame: At post-exercise session (single bout lasting 30 and 45 seconds)
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EPOC (kcal) will be measured using a portable indirect calorimetry system
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At post-exercise session (single bout lasting 30 and 45 seconds)
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Change in blood lactate concentration (BLa)
Time Frame: At pre- and post-exercise session (single bout) at 3 minutes post-exercise
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BLa (mmol/L) concentration will be measured in a microphotometer with commercially available kits.
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At pre- and post-exercise session (single bout) at 3 minutes post-exercise
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Change in heart rate
Time Frame: At pre-exercise, during, and post-exercise session (single bout lasting 30 and 45 seconds)
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Heart rate (bpm) will be measured with a wearable heart rate monitor
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At pre-exercise, during, and post-exercise session (single bout lasting 30 and 45 seconds)
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Change in perceived exertion
Time Frame: At pre-exercise, during, and post-exercise session (single bout lasting 30 and 45 seconds)
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Rating of perceived exertion (RPE) will be measured with the Borg scale (0-10)
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At pre-exercise, during, and post-exercise session (single bout lasting 30 and 45 seconds)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body weight
Time Frame: At baseline
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Body weight will be measured on a beam balance with stadiometer
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At baseline
|
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Body height
Time Frame: At baseline
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Body height will be measured on a beam balance with stadiometer
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At baseline
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Body mass index (BMI)
Time Frame: At baseline
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BMI will be calculated using the Quetelet's equation
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At baseline
|
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Waist circumference (WC)
Time Frame: At baseline
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WC (cm) will be measured using a Gullick II tape
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At baseline
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Hip circumference (HC)
Time Frame: At baseline
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HC (cm) will be measured using a Gullick II tape
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At baseline
|
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Waist-to-hip ratio (WHR)
Time Frame: At baseline
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WHR will be calculated by dividing the waist by the hip measurement
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At baseline
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Resting metabolic rate (RMR)
Time Frame: At baseline
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RMR (kcal) will be measured using a portable open-circuit indirect calorimeter with a ventilated hood system
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At baseline
|
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Fat-free mass (FFM)
Time Frame: At baseline
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FFM (kg) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)
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At baseline
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Maximal strength (1RM)
Time Frame: At baseline
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1RM (kg) will be measured bilaterally on a horizontal leg press and seated chest press machine..
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At baseline
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Muscular endurance
Time Frame: At baseline
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Muscular endurance (repetitions) will be measured on a 1-min curl-up and push-up test.
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At baseline
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Body fat (BF) Body fat (%) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)
Time Frame: At baseline
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BF (%) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)
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At baseline
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Fat mass (FM)t Body fat (%) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)
Time Frame: At baseline
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FM (kg) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)
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At baseline
|
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Maximal oxygen consumption (VO2max)
Time Frame: At baseline
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VO2max (mL/kg/min) will be assessed by a portable open-circuit spirometry system.
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At baseline
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Ioannis G. Fatouros, PhD, University of Thessaly
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- BWT-UTH
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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