Blood Flow Restriction and Recovery in Soccer Players

Sponsor
University of the Balearic Islands (Other)
Overall Status
Completed
CT.gov ID
NCT05097027
Collaborator
(none)
79
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2
7
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Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Blood flow restriction recovery
  • Other: Active recovery
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
79 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Effects of Blood Flow Restriction on Post-competition Recovery on Semi-professional and Youth Soccer Players
Actual Study Start Date :
Nov 1, 2021
Actual Primary Completion Date :
Nov 30, 2021
Actual Study Completion Date :
Jun 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Blood flow restriction recovery (Experimental I)

Active recovery program with blood flow restriction using a periodization methodology in soccer. (Post-match +1 training).

Device: Blood flow restriction recovery
Soccer players included in experimental group I will carry out this program for 1 week using 160mmHg blood pressure. 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.

Experimental: Non-Blood flow restriction recovery (Experimental II)

Active recovery program without blood flow restriction using a periodization methodology in soccer. (Post-match +1 training).

Other: Active recovery
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.

Outcome Measures

Primary Outcome Measures

  1. Change from Baseline in Countermovement Jump (CMJ) [Change from Baseline in countermovement Jump (CMJ Test) at 0 hours, 24 hours, 72 hours and 4 weeks]

    CMJ Test measured by Force Platform (Vald Performance, Brisbane, QLD)

Secondary Outcome Measures

  1. 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 weeks]

    Rating 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)

  2. Change from Baseline in Fatigue [Change from Baseline in Fatigue at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeks]

    Fatigue measured by a Wellness Questionary (1= Always tired; 2=More tired than normal; 3=Normal; 4= Fresh; 5= Very fresh)

  3. Change from Baseline in Muscle Soreness [Change from Baseline in Muscle Soreness at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeks]

    Muscle Soreness measured by a Wellness Questionary (1=Very sore; 2= Increase in soreness/ tightness; 3=Normal; 4=Feeling good; 5=Feeling great)

  4. Change from Baseline in Sleep Quality [Change from Baseline in Sleep Quality at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeks]

    Sleep Quality measured by a Wellness Questionary (1=Insomnia; 2=Restless sleep; 3=Difficulty falling asleep; 4=good; 5=Very restful)

  5. Change from Baseline in Stress [Change from Baseline in Stress at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeks]

    Stress measured by a Wellness Questionary (1=Highly stressed; 2=Feeling stressed; 3=Normal; 4=Relaxed; 5=Very relaxed)

  6. Change from Baseline in Mood [Change from Baseline in Stress at 0 hours, 24 hours, 48 hours, 72 hours and 4 weeks]

    Mood 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)

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years to 40 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 50 Minutes or more playing during the last match.
Exclusion Criteria:
  • No injuries players.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Christian Palma De Mallorca Balearic Islands Spain 07122

Sponsors and Collaborators

  • University of the Balearic Islands

Investigators

  • Principal Investigator: Christian Castilla López, University of Balearic Islands
  • Study Director: Natalia Romero Franco, PhD, University of Balearic Islands

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of the Balearic Islands
ClinicalTrials.gov Identifier:
NCT05097027
Other Study ID Numbers:
  • 221CER21
First Posted:
Oct 27, 2021
Last Update Posted:
Jun 21, 2022
Last Verified:
Jun 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of the Balearic Islands

Study Results

No Results Posted as of Jun 21, 2022