ClinicalTrials.gg
Status unknownNCT06477705FAMUpdated Jul 1, 2024

The Energy Cost of 1-Hour Football Training

An interventional study of FAM in Energy Expenditure, Body Composition and Resting Metabolic Rate, sponsored by University of Thessaly. Status unknown at 1 site in Greece. Open to male participants aged 40 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-07-01.

Sponsored by University of Thessaly · Not applicable, Interventional, and Other

The sponsor has not verified this record recently (last verified Jun 2024), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
40 Years to 60 Years
Sex
Male
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Energy Expenditure
  • Body Composition
  • Resting Metabolic Rate
  • Overweight and Obesity

Keywords

  • Football training
  • Energy Expenditure
  • Oxygen consumption
  • Blood lactate
  • Metabolic Syndrome
03

In context

Overweight

3,767 studies on the registry are indexed under Overweight; 863 are open to participants now.

This study's planned enrollment of 20 is below the median of 73 across 3,263 interventional studies indexed under Overweight.

Browse Overweight studies →

Lead sponsor

University of Thessaly is the lead sponsor of 194 studies on the registry; 43 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 60 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Musculoskeletal injury
  • Use of alcohol, caffeine and any type of ergogenic supplements or medication during the course of the study
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Investigator)
Enrollment
20 participants (estimated)

Study arms

  • 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.

    Other: FAM

Interventions

  • OtherFAM

    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

06

What researchers measure

Primary outcomes

  1. Change in exercise-induced energy expenditure

    Exercise energy expenditure (kcal) will be measured using a portable indirect calorimetry system

    Time frame: At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)

  2. Change in excess post-exercise oxygen consumption (EPOC)

    EPOC (kcal) will be measured using a portable indirect calorimetry system

    Time frame: At post-exercise session (single bout lasting 60 minutes)

  3. Change in blood lactate concentration (BLa)

    BLa (mmol/L) concentration will be measured in a microphotometer with commercially available kits.

    Time frame: At pre- and post-exercise session (single bout) at 3 minutes post-exercise

  4. Change in heart rate

    Heart rate (bpm) will be measured with a wearable heart rate monitor

    Time frame: At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)

  5. Change in perceived exertion

    Rating of perceived exertion (RPE) will be measured with the Borg scale (0-10)

    Time frame: At pre-exercise and post-exercise session (single bout lasting 60 minutes)

  6. Respiratory Exchange Ratio (RER)

    Respiratory Exchange Ratio (RER) will be measured using a portable indirect calorimetry system

    Time frame: At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)

  7. Breath Frequency (BF)

    Breath Frequency (BF) will be measured using a portable indirect calorimetry system

    Time frame: At pre-exercise, during, and post-exercise session (single bout lasting 60 minutes)

Secondary outcomes

  1. Body weight

    Body weight will be measured on a beam balance with stadiometer

    Time frame: At baseline

  2. Body height

    Body height will be measured on a beam balance with stadiometer

    Time frame: At baseline

  3. Body mass index (BMI)

    BMI will be calculated using the Quetelet's equation

    Time frame: At baseline

  4. Waist circumference (WC)

    WC (cm) will be measured using a Gullick II tape

    Time frame: At baseline

  5. Hip circumference (HC)

    HC (cm) will be measured using a Gullick II tape

    Time frame: At baseline

  6. Waist-to-hip ratio (WHR)

    WHR will be calculated by dividing the waist by the hip measurement

    Time frame: At baseline

  7. Resting metabolic rate (RMR)

    RMR (kcal) will be measured using a portable open-circuit indirect calorimeter with a ventilated hood system

    Time frame: At baseline

  8. Body fat (BF)

    Body fat (%) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)

    Time frame: At baseline

  9. Fat mass (FM)

    FM (kg) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)

    Time frame: At baseline

  10. Fat-free mass (FFM)

    FFM (kg) will be assessed by whole-body dual-energy X-ray absorptiometry (DXA)

    Time frame: At baseline

  11. Bone mass density

    Bone mass density will be measured by using Dual-emission X-ray absorptiometry

    Time frame: At baseline

  12. Bone mass content

    Bone mass content will be measured by using Dual-emission X-ray absorptiometry

    Time frame: At baseline

  13. Peak Maximal oxygen consumption (Peak VO2)

    Peak VO2 will be estimated by open circuit spirometry via breath by breath method

    Time frame: At baseline

  14. Dietary intake

    Dietary intake will be assesed over a 7-day period using diet recalls

    Time frame: At baseline

  15. Field activity during the soccer training

    The field activity will be continuously monitored during the soccer training using global positioning system (GPS)

    Time frame: [Time Frame: During the 60 minutes soccer training (ST) session (72 hours after baseline measurements)

  16. Systolic Blood Pressure

    Systolic Blood Pressure will be examined using sphygmomanometer

    Time frame: At baseline

  17. Dystolic Blood Pressure

    Dystolic Blood Pressure will be examined using sphygmomanometer

    Time frame: At baseline

  18. Rest Heart Rate

    The rest heart rate will be estimated using a heart rate monitor

    Time frame: At baseline

07

Study locations

1 of 1 sites recruiting
  • Laboratory of Exercise Physiology, Exercise Biochemistry and Sports Nutrition, School of Physical Education, Sports Sciences and Dietetics, University of Thessaly
    Trikala, 42100, Greece
    • Ioannis G Fatouros, Prof · Contact · ifatouros@pe.uth.gr · +30 24310 47047
    • Athanasios Z Jamurtas, Prof · Contact · ajamurt@pe.uth.gr · +30 24310 47047
    • Dimitrios Brisimitzis, MSc · Principal investigator
    Recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jun 2024 (actual). Primary completion is estimated for Jun 2024, 0 months after the start.

Of 1,356 non-industry interventional studies with no phase under Overweight, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 8 and three quarters within 38. This study's planned 0 months is below that.

Counting every sponsor, half of 1,472 studies reached it within 17 months; a quarter within 7 and three quarters within 36.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 21, 2024
First posted
Jun 27, 2024
StartActual
Jun 23, 2024
Primary completionEst.
Jun 28, 2024
CompletionEst.
Jul 8, 2024
Last update
Jul 1, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 1, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06477705
Responsible party
Ioannis G. Fatouros (Professor, University of Thessaly) — Principal investigator
First posted
Jun 27, 2024
Start date
Jun 23, 2024
Primary completion
Jun 28, 2024 (estimated)
Completion
Jul 8, 2024 (estimated)
Last update
Jul 1, 2024

Study contacts

Ioannis G Fatouros, Prof
Contact
ifatouros@.pe.uth.gr
+30 24310 47047
Athanasios Z Jamurtas, Prof
Contact
ajamurt@pe.uth.gr
+30 24310 47054
Ioannis G Fatouros
principal investigator · University of Thessaly

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion