The Energy Cost of 1-Hour Football Training (FAM)

June 28, 2024 updated by: Ioannis G. Fatouros, University of Thessaly

Energy Expenditure Induced by Football Training in Overweight Middle-aged Males

This study aims at investigating the energy expenditure following a single Football trainning session in middle aged males. The participants will perform a soccer training session [A single training session including 60 minutes of warm up, soccer technical exercises and small-sided game] and a cotrol trial (No intervention included, only daily measurements) in randomized, repeated measures, crossover design.

Study Overview

Detailed Description

Football is an intermittent sport with frequent activity changes and a high number of explosive movements. As a result, both mitochondrial and the non-mitochondrial energy sources (phosphagens, lactic acid system) are heavily utilized during football practice and games, which may contribute to the rise of oxygen consumption following exercise (EPOC) compared with cardiovascular-type exercise, where VO2 can reach a steady state.However, it is observed that there is a methodological limitation in the determination of total energy expenditure during and after football training and specifically in overwight middle-aged participans with metabolic syndrome.

Twenty overweight middle-aged males with mtabolic syndrome will perform a soccer training session [A single training session including 60 minutes of warm up, soccer technical exercises and small-sided game] and a cotrol trial (No intervention included, only daily measurements) in randomized, repeated measures, crossover design. Anthropometric, biochmeistry indicators, metabolic, blood pressure, physical activity and performance measurements will be measured at baseline. Global positoning system and accelerometry devices will be used to measure the distance and intensity of football trianing. The metabolic cost will be 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

Interventional

Enrollment (Estimated)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

  • Name: Athanasios Z Jamurtas, Prof
  • Phone Number: +30 24310 47054
  • Email: ajamurt@pe.uth.gr

Study Locations

      • Trikala, Greece, 42100
        • Recruiting
        • Laboratory of Exercise Physiology, Exercise Biochemistry and Sports Nutrition, School of Physical Education, Sports Sciences and Dietetics, University of Thessaly
        • Contact:
        • Principal Investigator:
          • Dimitrios Brisimitzis, MSc
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Free of musculoskeletal injuries
  • No use of ergogenic supplements or medication
  • Free of chronic diseases
  • age of 40-60 years
  • BMI>25
  • Metabolic syndrome

Exclusion Criteria:

  • Musculoskeletal injury
  • Use of alcohol, caffeine and any type of ergogenic supplements or medication during the course of the study

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: Other
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Participants in this arm will receive no intervention
Experimental: Recreational Football Training
Participants in this arm will participate in a football training session for 60 minutes. During the training the participans will execute the warm-up process, the part of soccer technical exercises and they will play a small-side-game.
Participants will perform a recreational Football Training session for 60 minutes. The training will include the warm-up, soccer technical exercises and a small-side game

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in blood lactate concentration (BLa)
Time Frame: At pre- and post-exercise session (single bout) at 3 minutes post-exercise
BLa (mmol/L) concentration will be measured in a microphotometer with commercially available kits.
At pre- and post-exercise session (single bout) at 3 minutes post-exercise
Change in exercise-induced energy expenditure
Time Frame: At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)
Exercise energy expenditure (kcal) will be measured using a portable indirect calorimetry system
At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)
Change in excess post-exercise oxygen consumption (EPOC)
Time Frame: At post-exercise session (single bout lasting 60 minutes)
EPOC (kcal) will be measured using a portable indirect calorimetry system
At post-exercise session (single bout lasting 60 minutes)
Change in heart rate
Time Frame: At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)
Heart rate (bpm) will be measured with a wearable heart rate monitor
At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)
Change in perceived exertion
Time Frame: At pre-exercise and post-exercise session (single bout lasting 60 minutes)
Rating of perceived exertion (RPE) will be measured with the Borg scale (0-10)
At pre-exercise and post-exercise session (single bout lasting 60 minutes)
Respiratory Exchange Ratio (RER)
Time Frame: At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)
Respiratory Exchange Ratio (RER) will be measured using a portable indirect calorimetry system
At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)
Breath Frequency (BF)
Time Frame: At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)
Breath Frequency (BF) will be measured using a portable indirect calorimetry system
At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body weight
Time Frame: At baseline
Body weight will be measured on a beam balance with stadiometer
At baseline
Body height
Time Frame: At baseline
Body height will be measured on a beam balance with stadiometer
At baseline
Body mass index (BMI)
Time Frame: At baseline
BMI will be calculated using the Quetelet's equation
At baseline
Waist circumference (WC)
Time Frame: At baseline
WC (cm) will be measured using a Gullick II tape
At baseline
Hip circumference (HC)
Time Frame: At baseline
HC (cm) will be measured using a Gullick II tape
At baseline
Waist-to-hip ratio (WHR)
Time Frame: At baseline
WHR will be calculated by dividing the waist by the hip measurement
At baseline
Resting metabolic rate (RMR)
Time Frame: At baseline
RMR (kcal) will be measured using a portable open-circuit indirect calorimeter with a ventilated hood system
At baseline
Fat mass (FM)
Time Frame: At baseline
FM (kg) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)
At baseline
Fat-free mass (FFM)
Time Frame: At baseline
FFM (kg) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)
At baseline
Dietary intake
Time Frame: At baseline
Dietary intake will be assesed over a 7-day period using diet recalls
At baseline
Peak Maximal oxygen consumption (Peak VO2)
Time Frame: At baseline
Peak VO2 will be estimated by open circuit spirometry via breath by breath method
At baseline
Bone mass density
Time Frame: At baseline
Bone mass density will be measured by using Dual-emission X-ray absorptiometry
At baseline
Bone mass content
Time Frame: At baseline
Bone mass content will be measured by using Dual-emission X-ray absorptiometry
At baseline
Systolic Blood Pressure
Time Frame: At baseline
Systolic Blood Pressure will be examined using sphygmomanometer
At baseline
Dystolic Blood Pressure
Time Frame: At baseline
Dystolic Blood Pressure will be examined using sphygmomanometer
At baseline
Rest Heart Rate
Time Frame: At baseline
The rest heart rate will be estimated using a heart rate monitor
At baseline
Body fat (BF)
Time Frame: At baseline
Body fat (%) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)
At baseline
Field activity during the soccer training
Time Frame: [Time Frame: During the 60 minutes soccer training (ST) session (72 hours after baseline measurements)
The field activity will be continuously monitored during the soccer training using global positioning system (GPS)
[Time Frame: During the 60 minutes soccer training (ST) session (72 hours after baseline measurements)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ioannis G Fatouros, University of Thessaly

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)

June 23, 2024

Primary Completion (Estimated)

June 28, 2024

Study Completion (Estimated)

July 8, 2024

Study Registration Dates

First Submitted

June 21, 2024

First Submitted That Met QC Criteria

June 21, 2024

First Posted (Actual)

June 27, 2024

Study Record Updates

Last Update Posted (Actual)

July 1, 2024

Last Update Submitted That Met QC Criteria

June 28, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

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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