The Impact of Blood Flow Restriction Within Warm-up.

December 4, 2023 updated by: University Ghent

The Impact of Blood Flow Restriction Within Warm-up Routines on Performance and Muscle Stiffness.

Sixty athletes will be randomized in two groups; (1) an experimental group and (2) a control group. Both groups will undergo the following procedure:

Moment 1:

  1. Baseline testing: countermovement jump, 25m sprint and strength assessment of the Hamstrings and Quadriceps muscle.
  2. Short warm-up (approximately 4 minutes), which will be completed with blood flow restriction cuffs (experimental group) or without (control group)
  3. Post testing: same tests as performed in baseline.

Moment 2:

  1. Baseline testing: stiffness measurements of the Biceps Femoris Long Head via Shear Wave Elastography.
  2. Short warm-up (approximately 4 minutes), which will be completed with blood flow restriction cuffs (experimental group) or without (control group)
  3. Post testing: same tests as performed in baseline.

Both moments of testing as well as the order in which the performance tests take place are randomized.

Study Overview

Detailed Description

Traditionally, athletes perform a warm-up program before participating in sport activities, due to its assumed beneficial effect on performance and injury prevention. However, within team sports, substitutes usually do not perform the comprehensive pre-match warm-up. In many cases, those substitute players get a very short period of time, during the game, to prepare themselves for coming on to the pitch where they immediately have to perform at a very high-intensity. Hence, this could lead to a poorer performance and a greater injury risk for those substitute players, as they did not get a decent warm-up.

Therefore, new techniques are needed in order to prepare the substitute athletes optimally in a very short period of time (often within a few minutes). Consequently, the aim of this study is to investigate whether the incorporation of Blood Flow Restriction (BFR) within a warm-up routine could be of additional value. Both performance parameters and muscle stiffness will be evaluated. As Hamstring strain Injuries (HSI) are common within sports encompassing high-speed running, this muscle group will be investigated on muscle stiffness as a representation of the interventional effect on muscle stiffness. Athletes will be randomized in two groups of 30 participants (anticipated); (1) an experimental group and (2) a control group. Both groups will perform baseline testing (5x Countermovement Jump, 25m Sprint and Muscle Strength of hamstrings and Quadriceps), and a short warm-up program, followed by repeating the same tests as executed in baseline. The experimental group will receive Blood Flow Restriction within the warm-up routine, whereas the control group will do the same warm up program but without BFR.

On a separate occasion, the same athletes will perform the same warm-up routine with a Shear Wave Elastographic assessment of the Biceps Femoris Long Head before and after (immediately after, after 5 minutes and once more after 10 minutes) the warm-up.

Study Type

Interventional

Enrollment (Actual)

60

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

      • Ghent, Belgium, 9000
        • Ghent University

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

18 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Free of pain at the moment of testing
  • Adult (18+)
  • Athletes (competitive team sport)

Exclusion Criteria:

  • History of a hamstring strain injury
  • History of cardiovascular problems
  • Recent (<1 year) trauma or surgery of the lower extremity
  • Reduced functioning or pain in the lower extremity.
  • Not being able to perform physical activities, for whatever (medical) reason.

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Blood Flow Restriction
Incorporation of Blood Flow Restriction within the warm-up routine.
Blood Flow Restriction
Other Names:
  • Kaatsu
  • partial vascular occlusion
Active Comparator: Control Group
Warm-up routine without any special intervention (no Blood Flow Restriction).
Warm-up without any special intervention (no Blood Flow Restriction)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in muscle stiffness
Time Frame: (1) Before the warm-up routine, (2) immediately after the warm-up routine, (3) 5 minutes after the warm-up routine, and (4) 10 minutes after the warm-up routine
The stiffness of the Biceps Femoris Long Head of the dominant leg will be assessed via a Shear Wave Elastography Device (Mach 30, SuperSonic Imagine), before and immediately after the warm-up routine. The muscle stiffness will be expressed in Kilopascals (kPa).
(1) Before the warm-up routine, (2) immediately after the warm-up routine, (3) 5 minutes after the warm-up routine, and (4) 10 minutes after the warm-up routine
Change in jump height
Time Frame: (1) Before the warm-up routine and (2) immediately after the warm-up routine
The jump height will be assessed during 5 consecutive countermovement jumps. This will be assessed with an OptoJump device. The highest jump will be taken into account. The jump height will be expressed in cm.
(1) Before the warm-up routine and (2) immediately after the warm-up routine
Change in muscle strength
Time Frame: (1) Before the warm-up routine and (2) immediately after the warm-up routine
Muscle strength of the Hamstrings and Quadriceps muscles. Measured via a Hand Held Dynamometer. Strength will be expressed in Newton (N).
(1) Before the warm-up routine and (2) immediately after the warm-up routine
Change in sprinting speed
Time Frame: (1) Before the warm-up routine and (2) immediately after the warm-up routine
Sprinting speed will be assessed at 5m, 10m and 25m. This via the use of timing gates. This outcome measure will be expressed in seconds (s).
(1) Before the warm-up routine and (2) immediately after the warm-up routine

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
level of readiness
Time Frame: Immediately after the warm-up
Participants will be asked after the warm-up (with or without BFR) how well they feel prepared to substitute into the game on a scale from 0-100; being zero = not ready at all, 100 = totally ready
Immediately after the warm-up
Change in heart rate
Time Frame: (1) Right before the warm up, (2) after one minute, (3) after two minutes, (4) after 3 minutes, (5) at the end of the warm up
This parameter will be captured to track the cardiovascular answer of the body during the warm-up by using a polar watch and elastic strap with a monitor around the waist.
(1) Right before the warm up, (2) after one minute, (3) after two minutes, (4) after 3 minutes, (5) at the end of the warm up

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Erik Witvrouw, Departement of Rehabilitation Sciences, Ghent University

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)

November 2, 2021

Primary Completion (Actual)

November 30, 2023

Study Completion (Actual)

November 30, 2023

Study Registration Dates

First Submitted

November 15, 2021

First Submitted That Met QC Criteria

November 29, 2021

First Posted (Actual)

December 10, 2021

Study Record Updates

Last Update Posted (Actual)

December 5, 2023

Last Update Submitted That Met QC Criteria

December 4, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • B6702021000931

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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