ClinicalTrials.gg
CompletedNCT03348267PRO-FOOTBALLUpdated Jan 30, 2018

Protein Supplementation and Muscle Recovery in Football

An interventional study of Milk protein isolate and Placebo in Skeletal Muscle Damage, Muscle Inflammation and Muscle Recovery, sponsored by University of Thessaly. Completed at 1 site in Greece. Open to male participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-01-30.

Sponsored by University of Thessaly · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 1 year 6 months after the study started (first participant enrolled May 2016, registered Nov 2017).

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Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years to 25 Years
Sex
Male
01

Study summary

Soccer is an intermittent sport including a high number of powerful actions such as accelerations, decelerations, changes of direction, jumps and impacts that incorporate a strong eccentric component and may therefore lead to skeletal muscle damage. Indeed, match activity is associated with the onset of muscle damage and an acute inflammatory response that result in attenuated performance for as long as 1 to 3 days. In competitive soccer though, multiple matches are performed within a small-time frame resulting in inadequate muscle recovery and reduced field performance. Supplementation with milk proteins following intense exercise protocols has been shown to stimulate protein synthesis and facilitate muscle recovery. Thus, the aim of the present investigation is to examine the effects of milk protein supplementation on muscle recovery and soccer-specific performance during an in-season microcycle with two matches performed three days apart.

Read the detailed description

In a double-blind, cross over, repeated measures design 20 men soccer players will receive either placebo (PLA) or milk protein isolate (PRO, 80% casein-20% whey) throughout recovery following two matches performed three days apart. On match days, players will receive a dose immediately after the match (PLA vs PRO: 25g of protein) and then at 3h (PLA vs PRO: 30g of protein) and 6h (PLA vs PRO: 25g of protein) post-match. On each day of the remaining days, players will consume a single dose of PLA or PRO (20g of protein) with breakfast. All players will participate in regular in-season training following matches. Field activity during both matches and daily practices will be monitored using GPS devices. Heart rate will be continuously recorded during each match and training session. Blood samples will be collected at baseline as well as 2 hours after the first match, daily for three days after the first match, 2 hours after the second match and daily for 3 days after the second match. Performance (isokinetic strength, 20-m speed, repeated sprint ability) and muscle soreness will be assessed at baseline daily for 3 days after both matches. Muscle biopsies from vastus lateralis will be collected at baseline and one day after each match.

02

Conditions studied

  • Skeletal Muscle Damage
  • Muscle Inflammation
  • Muscle Recovery
  • Soccer Performance
03

In context

Myositis, Inclusion Body

65 studies on the registry are indexed under Myositis, Inclusion Body; 10 are open to participants now.

This study's enrollment of 20 is below the median of 30 across 42 interventional studies indexed under Myositis, Inclusion Body.

Browse Myositis, Inclusion Body studies →

Lead sponsor

University of Thessaly is the lead sponsor of 195 studies on the registry; 44 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 25 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

  • i) participation at elite level (top three division leagues) of soccer competition for at least five years, ii) abstain from consumption of performance-enhancing supplements, antioxidant supplements and medications (for at least 6 months before and during the study), iv) participate in at least six two-hour training sessions per week and played at least one match per week and v) non-smokers.

Exclusion criteria

Exclusion Criteria:

  • i) a known milk intolerance or allergy, ii) a recent febrile illness, iii) history of muscle lesion, iv) lower limb trauma and v) metabolic diseases.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Investigator)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    Protein

    On the match day, 25g of protein consumed immediately after the match and then 30g at 3h (+3h) and 25g at 6h (+6h). On each day of the remaining days, 20 g of protein consumed with breakfast.

    Dietary Supplement: Milk protein isolate

  • Active comparator
    Placebo

    On the match day, 500 ml received received orally immediately post-match and then at +3h and +6h. On the remaining days, 500 ml daily with breakfast.

    Dietary Supplement: Placebo

Interventions

  • Dietary supplementMilk protein isolate

    Milk protein isolate in a powder form consisted of 80% casein and 20% whey protein. 20g were diluted into 500 ml water

  • Dietary supplementPlacebo

    500 mL drink that contained water (375 mL), sugar-free cordial (125 mL) and 2 g of low-calorie glucose/dextrose powder.

06

What researchers measure

Primary outcomes

  1. Change in creatine kinase in plasma

    Concentration of creatine kinase will be measured in plasma

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  2. Change in uric acid in plasma

    Concentration of uric acid will be measured in plasma

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  3. Change in protein carbonyls in blood

    Concentration of protein carbonyls will be measured in red blood cells

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  4. Change in total antioxidant capacity

    Total antioxidant capacity will be measured in plasma

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  5. Change in reduced glutathione in blood

    Concentration of reduced glutathione will be measured in in red blood cells

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  6. Change in oxidized glutathione in blood

    Concentration of oxidized glutathione will be measured in red blood cells

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  7. Change in malondialdehyde in blood

    Concentration of malondialdehyde will be measured in serum

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  8. Change in catalase activity

    Catalase activity will be measured in red blood cells

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  9. Change in protein carbonyls in muscle

    Concentration of protein carbonyls will be measured in muscle

    Time frame: At baseline, 24h post-Match 1 and 24h post-Match 2

  10. Change in intracellular signaling proteins in muscle

    Phosphorylation levels of Akt, mammalian target of rapamycin (mTOR) and p70S6K will be measure using western blotting.

    Time frame: At baseline, 24h post-Match 1 and 24h post-Match 2

  11. Change in proteasome activities in muscle

    Chymotrypsin-like (CT-L), caspase-like (C-L) and trypsin-like (T-L) proteasome activities will be assayed with hydrolysis of the fluorogenic peptide LLVY-AMC, LLE-AMC and LSTR-AMC, respectively.

    Time frame: At baseline, 24h post-Match 1 and 24h post-Match 2

  12. Change in satellite cells in muscle

    Pax7, Myf5, MyoD and Myogenin will be measured in order to quantify quiescent, activated, proliferated-differentiated and fused satellite cells respectively.

    Time frame: At baseline, 24h post-Match 1 and 24h post-Match 2

  13. Change in repeated Sprint Ability

    5 x 30 m sprints will be performed with 25 seconds rest in-between. Mean time for 5 sprints and fatigue index will be calculated.

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  14. Change in countermovement jump

    Countermovement jump will be assessed on a contact platform

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  15. Change in isokinetic strength of lower limbs

    Isokinetic strength will be assessed on an isokinetic dynamometer for both knee extensors and knee flexors at 120 and 180 degrees.

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  16. Change in match activity

    Match activity will be continuously recorded during both matches using GPS technology.

    Time frame: During Match 1 and Match 2

  17. Change in heart rate

    Heart rate will be continuously recorded during both matches using the Team Polar system.

    Time frame: During Match 1 and Match 2

Secondary outcomes

  1. Change in delayed onset of muscle soreness

    Muscle soreness will assessed during palpation of the muscle belly and the distal region of relaxed vastus medialis, vastus lateralis and rectus femoris following three repetitions of of a full squat. Subjects will rate their DOMS on a visual analogue scale (0-10).

    Time frame: At baseline, at 24h, 48h and 72h post-Match 1 as well as at 24h, 48h and 72h post-Match 2

  2. Dietary intake

    Dietary intake will be assessed using 7-day diet recalls.

    Time frame: Over a 7-day period at baseline.

  3. Change in white blood cell count.

    White blood cell count will be measured using an automatic blood analyzer.

    Time frame: At baseline, immediately after Match 1, at 24h, 48h and 72h post-Match 1 as well as immediately after Match 2 and at 24h, 48h and 72h post-Match 2.

07

Study locations

1 site
  • Exercise Biochemistry Laboratory, School of Physical Education & Sports Sciences, University of Thessaly
    Tríkala, 42100, Greece
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from May 2016 to primary completion in Jun 2016, 1 month.

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

Registered
Nov 15, 2017
First posted
Nov 20, 2017
StartActual
May 1, 2016
Primary completionActual
Jun 30, 2016
CompletionActual
Sep 15, 2016
Last update
Jan 30, 2018
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 Jan 30, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03348267
Responsible party
Athanasios Z. Jamurtas (Professor, University of Thessaly) — Principal investigator
First posted
Nov 20, 2017
Start date
May 1, 2016
Primary completion
Jun 30, 2016
Completion
Sep 15, 2016
Last update
Jan 30, 2018

Study contacts

ATHANASIOS POULIOS, PhDc
principal investigator · UNIVERSITY OF THESSALY, SCHOOL OF PHYSICAL EDUCATION & SPORTS SCIENCES

Oversight

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

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