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Blood Flow Restriction and Recovery in Soccer Players

Effects of Blood Flow Restriction on Post-competition Recovery on Semi-professional and Youth Soccer Players

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05097027
Enrollment
40
Registered
2021-10-27
Start date
2021-11-01
Completion date
2022-06-01
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Resistance Training, Recovery

Keywords

Soccer, Blood Flow Restriction, Performance, Active recovery

Brief summary

The objective is to evaluate the effects of blood flow restriction training on the post-competition recovery of professional and semi-professional soccer players. Randomized crossover clinical trial, with two intervention groups: Experimental group I will carry out a recovery training based on the use of the blood flow restriction (BFR) on day 1 post-competition. On the other hand, the Experimental II group will perform the same recovery training without the use of BFR. After 1 month the groups will cross their intervention and make the recovery with the opposite method to the initial one. The study will be carried out during the 2021-2022 season, from first regional to third division of Spanish soccer, with soccer teams from the Mallorca Island. Before the competition, the countermovement jump (CMJ) will be evaluated and repeated at 0, 24, and 72 h after the competition. The levels of muscle soreness (DOMS) will be evaluated pre-post-competition 0, 24, 48 and 72h later. The same procedure will be carried out to evaluate muscle fatigue, sleep quality, and stress through a questionnaire that athletes will fill out pre, 0, 24, 48 and 72h after the game. Sociodemographic and anthropometric data will be collected before starting the study.

Detailed description

W-UP: The warm-up will consist of 5 minutes running slow, 5 minutes mobility, and 5 minutes of running exercises. In addition, the warm-up will contain a familiarization with the jump test.

Interventions

DEVICEBlood flow restriction recovery

Soccer players included in experimental group I will carry out this program for 1 week setting the blood pressure to \ 60% of limb occlusion pressure (LOP). After a month they will carry out the program without restriction of blood flow. Which will consist of a warm-up part with continuous running (5 min), 6 sprints from box to box of the field at 60-70% of a maximum repetition, and an activation part in the form of rounds with the ball.

Soccer players included in experimental group II will carry out this program for 1 week. After a month they will carry out the program with blood flow restriction. Which will consist of a warm-up part with continuous running (5 min), 6 sprints from box to box of the field at 60-70% of a maximum repetition, and an activation part in the form of rounds with the ball.

Sponsors

University of the Balearic Islands
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
MALE
Age
14 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* 50 Minutes or more playing during the last match.

Exclusion criteria

* No injuries players.

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in Countermovement Jump (CMJ)Change from Baseline in countermovement Jump (CMJ Test) at 0 hours, 24 hours, 72 hours and 4 weeksCMJ Test measured by Force Platform (Vald Performance, Brisbane, QLD)

Secondary

MeasureTime frameDescription
Change from Baseline in FatigueChange from Baseline in Fatigue at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeksFatigue measured by a Wellness Questionary (1= Always tired; 2=More tired than normal; 3=Normal; 4= Fresh; 5= Very fresh)
Change from Baseline in Muscle SorenessChange from Baseline in Muscle Soreness at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeksMuscle Soreness measured by a Wellness Questionary (1=Very sore; 2= Increase in soreness/ tightness; 3=Normal; 4=Feeling good; 5=Feeling great)
Change from Baseline in Rating of Perceived Exertion (RPE)Change from Baseline in RPE at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeksRating of Perceived Exertion (RPE) measured by Borg scale (0=Rest; 1=Really easy; 2=easy; 3=moderate; 4=sort of hard; 5=hard; 6=hard; 7=Really hard; 8= Really hard; 9= Really, really, hard; 10= Maximal)
Change from Baseline in StressChange from Baseline in Stress at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeksStress measured by a Wellness Questionary (1=Highly stressed; 2=Feeling stressed; 3=Normal; 4=Relaxed; 5=Very relaxed)
Change from Baseline in MoodChange from Baseline in Stress at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeksMood measured by a Wellness Questionary (1=Highly annoyed / irritable / down; 2=Snappy with team-mates, family and friends; 3=Less interested in others / activities; 4=Generally good mood; 5=Very positive mood)
Change from Baseline in Sleep QualityChange from Baseline in Sleep Quality at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeksSleep Quality measured by a Wellness Questionary (1=Insomnia; 2=Restless sleep; 3=Difficulty falling asleep; 4=good; 5=Very restful)

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026