Blood Flow Restriction Strength Training in Professional Soccer Players

May 31, 2023 updated by: University of the Balearic Islands

Effects of Blood Flow Restriction Resistance Training on Muscle Characteristics, Strength and Performance of Professional Soccer Players

The aims of this clinical study are evaluated the effects of Blood Flood Restriction training on the sport performance of professional and semi-professional soccer players. The participants are twenty male professional and semi-professional soccer players who are playing at RCD Mallorca. Participants will be assigned in two different groups. Both groups develop for six weeks a strength training programs. The first group will base their training in Low Load using Blood Flow Restriction (20-50% of one maximum repetition). The second group will base their training in High Load (60-80% of one maximum repetition). This training program includes three type of exercises in each training session; back squat, single deadlift and barbell hip thrust. Before and after this program the investigators will collect sociodemographic and anthropometrics data. On top of that, the investigators will evaluate the muscle mass, the electrical activity produced by skeletal muscles, the muscle strength and the sprint ability of every participant. Before to the evaluation, the soccer players will warm-up during 15 minutes under the control of the evaluators.

Study Overview

Detailed Description

PARTICIPANTS:

Participants are soccer players of RCD Mallorca (Second Spanish Football Division) and RCD Mallorca B (Third Spanish Football Division).Before to start the study, every participant will receive an informed consent about the clinical study. This informed consent will be signed by them according to Declaration of Helsinki. At the same time, the data will be anonymized and only the main researcher of the study will have access to it, to ensure compliance with the Data Protection Law.

W-UP:

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

Study Type

Interventional

Enrollment (Actual)

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 Locations

    • Balearic Islands
      • Palma De Mallorca, Balearic Islands, Spain, 07122
        • Christian

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

14 years to 40 years (Child, Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • No injuries in the last 6 months
  • 1 years experience minimun in the division.

Exclusion Criteria:

  • Amateurs players

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Strength training based on low loads with blood flow restriction (Experimental group I)
  1. Squat
  2. Single Deadlift
  3. Back Squat
Low Load (20-50% 1RM), 4 set of 30/15/15/15 repetitions, 30 seconds resting between sets.
Experimental: Strenght training based on high loads (Experimental group II)
  1. Squat
  2. Single Deadlift
  3. Back Squat
High Load (60-80% 1RM) 4 sets of 8 repetitions, 2 minutes resting between sets

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline in Muscle Mass
Time Frame: Change from Baseline in Muscle Mass at 6 Weeks
Muscle Mass mesured with measuring tape
Change from Baseline in Muscle Mass at 6 Weeks
Change from Baseline in Maximum Voluntary Isometric Contraction (MVIC)
Time Frame: Change from Baseline in Maximum voluntary Isometric Contraction at 6 Weeks
MVIC mesured by Force Platform (Vald Performance, Brisbane, QLD)
Change from Baseline in Maximum voluntary Isometric Contraction at 6 Weeks
Change from Baseline in Electrical Muscle Activity
Time Frame: Change from Baseline in Electrical Muscle Activity at 6 weeks
Electrical Muscle Activity mesured by Surface Electromyography (mDurance®, España)
Change from Baseline in Electrical Muscle Activity at 6 weeks
Change from Baseline in Countermovement Jump (CMJ)
Time Frame: Change from Baseline in countermovement Jump (CMJ Test) at 6 weeks
CMJ Test measured by Force Platform (Vald Performance, Brisbane, QLD)
Change from Baseline in countermovement Jump (CMJ Test) at 6 weeks
Change from in Force-Velocity Profile (F-V)
Time Frame: Change from Baseline in Force-Velocity Profile at 6 Weeks
F-V Profile measured by MyJump App
Change from Baseline in Force-Velocity Profile at 6 Weeks
Change from Baseline in Sprint Ability
Time Frame: Change from Baseline in Sprint Ability at 6 weeks
Sprint Ability measured by MySprint App
Change from Baseline in Sprint Ability at 6 weeks
Change from Post-Intervention in Sport Injuries Incidence
Time Frame: Change from Post-Intervention up to 8 months.
Incidence of injuries related to sport practice
Change from Post-Intervention up to 8 months.

Collaborators and Investigators

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

Investigators

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

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)

October 5, 2020

Primary Completion (Actual)

November 30, 2020

Study Completion (Actual)

November 30, 2020

Study Registration Dates

First Submitted

October 28, 2020

First Submitted That Met QC Criteria

November 13, 2020

First Posted (Actual)

November 16, 2020

Study Record Updates

Last Update Posted (Estimated)

June 2, 2023

Last Update Submitted That Met QC Criteria

May 31, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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