- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05523674
Effects of Warm-up Intensity and Blood Flow Restriction
May 27, 2025 updated by: Franciele Marques Vanderle, Paulista University
Effects of Warm-up Intensity and Blood Flow Restriction: A Randomized Controlled Clinical Trial
Introduction: warming up has the function of preparing the body structures for a given task to be performed during sports, increasing body and muscle temperature, focusing on improving performance.
Therefore, the use of the blood flow restriction technique (BFR) can be seen as a promising alternative for promoting greater mechanical and muscular stress, thus providing a more efficient warm-up and optimizing performance.
Objectives: to analyze the effects of RFS used during low-intensity warm-up compared with low-intensity and high-intensity warm-up without RFS on performance (jump test and 30-meter sprint test) and skin surface temperature.
In addition to analyzing and comparing, after the warm-up protocols with and without RFS, the acute responses on perceptual outcomes (perception of pain, change in sensitivity, subjective perception of exertion and perception of discomfort in relation to RFS) and muscle outcomes (tonus , muscle stiffness and elasticity).
Methods: a randomized controlled clinical trial will be carried out, with 33 amateur soccer players aged between 18 and 35 years who will be randomly divided into three groups: low-intensity warm-up without RFS (30% VO2max), high-intensity warm-up without RFS ( 80% VO2max) and low-intensity warm-up associated with BFR (80% of total occlusion pressure) [30% VO2max-BFR].
All groups will carry out the heating protocol and the outcomes will be evaluated at baseline and immediately after the end of the heating, as well as 10 and 20 minutes after its completion, namely: skin surface temperature through thermography; tone, stiffness and muscle elasticity by myotometry, subjective perception of pain (VAS); pain threshold through the pressure algometer; subjective perception of exertion (BORG scale); perception of discomfort in relation to RFS (LIKERT-CR-10 scale); 30-meter sprints measured through photocells and vertical jump, measured through the force platform.
Descriptive statistics will be used and comparisons will be made using the generalized linear mixed model, assuming a significance level of p<0.05.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
108
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
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SP
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Presidente Prudente, SP, Brazil, 55
- Franciele Marques Vanderlei
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São Paulo
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Presidente Prudente, São Paulo, Brazil, 19060-900
- Carlos Alberto Toledo Teixeira Filho
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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 35 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- male
- healthy
- amateur soccer player
- aged between 18 and 35 years
Exclusion Criteria:
- smokers;
- alcoholics;
- use drugs that influenced cardiac autonomic activity;
- cardiovascular, metabolic or endocrine diseases;
- having one or more predisposing risk factors for thromboembolism;
- history of lower extremity surgery or musculoskeletal injury within the last six months that may impair your performance during testing or warm-up (e.g., meniscal repair, ligament reconstruction, muscle injury, tendinopathy, lower extremity patellofemoral pain, and/or back pain);
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: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: warm-up performed at 80% VO2max
The warm-up exercise will be performed on an ergometric treadmill, through a protocol of 15 minutes duration, with the first 5 minutes of acceleration, until reaching 80% of VO2max, the following 5 minutes of maintenance and the remaining 5 minutes being of slowdown.
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The warm-up exercise will be performed on a treadmill.
Other Names:
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Experimental: warm-up performed at 30% VO2max
The warm-up exercise will be performed on an ergometric treadmill, through a protocol of 15 minutes duration, with the first 5 minutes of acceleration, until reaching 30% of VO2max, the following 5 minutes of maintenance and the remaining 5 minutes being of slowdown.
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The warm-up exercise will be performed on a treadmill.
Other Names:
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Experimental: warm-up performed at 30% VO2max with Blood Flow Restriction
The warm-up exercise will be performed on an ergometric treadmill, through a protocol of 15 minutes of duration, with the first 5 minutes of acceleration, until reaching 30% of VO2max, the following 5 minutes of maintenance and the remaining 5 minutes being of slowdown.
During the warm-up exercise, a pressure cuff will be used on each leg, with the blood flow restriction technique (80% of arterial occlusion pressure).
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The warm-up exercise will be performed on a treadmill and pressure cuffs will be used for the blood flow restriction technique.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Temperature
Time Frame: At the baseline
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Skin surface temperature will be evaluated using a thermographic camera
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At the baseline
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Temperature
Time Frame: Immediately after warm-up
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Skin surface temperature will be evaluated using a thermographic camera
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Immediately after warm-up
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Performance in Squat Jump Test
Time Frame: At the baseline
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The squat jump test will be performed at jumping platform (Multisprint, Hidrofit, Brazil)
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At the baseline
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Performance in Squat Jump Test
Time Frame: Immediately after warm-up
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The squat jump test will be performed at jumping platform (Multisprint, Hidrofit, Brazil)
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Immediately after warm-up
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Performance in 30 meter sprint
Time Frame: At the baseline
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the sprint test will be performed in a hall and two pairs of photoelectric cells (Multisprint®, Hidrofit, Brazil) will be used with an accuracy of 0.01 seconds.
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At the baseline
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Performance in 30 meter sprint
Time Frame: Immediately after warm-up
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the sprint test will be performed in a hall and two pairs of photoelectric cells (Multisprint®, Hidrofit, Brazil) will be used with an accuracy of 0.01 seconds.
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Immediately after warm-up
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Pain threshold
Time Frame: At the baseline
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To assess the pain threshold, the pressure algometer will be applied at 10 specific locations on the lower limb
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At the baseline
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Pain threshold
Time Frame: Immediately after warm-up
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To assess the pain threshold, the pressure algometer will be applied at 10 specific locations on the lower limb
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Immediately after warm-up
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Muscle Pain
Time Frame: At the baseline
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The subjective evaluation of pain will be obtained through the Visual Analogue Scale (VAS), graded from 0 to 10, with zero being the total absence of pain and 10 the maximum level of pain supported by the participan
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At the baseline
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Muscle Pain
Time Frame: Immediately after warm-up
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The subjective evaluation of pain will be obtained through the Visual Analogue Scale (VAS), graded from 0 to 10, with zero being the total absence of pain and 10 the maximum level of pain supported by the participan
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Immediately after warm-up
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Perceived Effort Scale (Borg)
Time Frame: At the baseline and Immediately after warm-up
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The degree of subjective exertion reported by the participants in relation to the lower limbs will be analyzed by Borg's scale of perception of effort of 0 to 10 points, 0 being "very easy" and 10 being "exhaustive."
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At the baseline and Immediately after warm-up
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Resistance through Bioimpedance analysis (BIA)
Time Frame: At the baseline and Immediately after warm-up
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Evaluation of tissue resistance, the higher the value, the worse the result
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At the baseline and Immediately after warm-up
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Reactance through Bioimpedance analysis (BIA)
Time Frame: At the baseline and Immediately after warm-up
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Evaluation of tissue reactance, the higher the value, the better the cell integrity
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At the baseline and Immediately after warm-up
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Phase angle through Bioimpedance analysis (BIA)
Time Frame: At the baseline and Immediately after warm-up
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Assessment of the phase angle, the higher the value, the better the condition of the participant
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At the baseline and Immediately after warm-up
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Tone muscular through Myotonometry used the MyotonPRO equipment
Time Frame: At the baseline and Immediately after warm-up
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Natural Oscillation Frequency [Hz], characterizing Tone of the muscles: quadriceps femoris, biceps femoris, semitendinosus, triceps surae and tibialis anterior
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At the baseline and Immediately after warm-up
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Stiffness through Myotonometry used the MyotonPRO equipment
Time Frame: At the baseline and Immediately after warm-up
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Mechanical Stress Relaxation Time [ms] featuring muscle elasticity of the muscles: quadriceps femoris, biceps femoris, semitendinosus, triceps surae and tibialis anterior
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At the baseline and Immediately after warm-up
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heart rate variability indices in the time domain
Time Frame: At the baseline time (30 minutes rest in the supine position), during the warm-up (15 minutes in the treadmill) and immediately after the warm-up (60 minutes rest in the supine position)
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Mean RR, SDNN e rMSSD
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At the baseline time (30 minutes rest in the supine position), during the warm-up (15 minutes in the treadmill) and immediately after the warm-up (60 minutes rest in the supine position)
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heart rate variability indices in the frequency domain
Time Frame: At the baseline time (30 minutes rest in the supine position), during the warm-up (15 minutes in the treadmill) and immediately after the warm-up (60 minutes rest in the supine position)
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LF and HF in nu and ms2
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At the baseline time (30 minutes rest in the supine position), during the warm-up (15 minutes in the treadmill) and immediately after the warm-up (60 minutes rest in the supine position)
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heart rate variability indices analyzed in the Poincaré plot
Time Frame: At the baseline time (30 minutes rest in the supine position), during the warm-up (15 minutes in the treadmill) and immediately after the warm-up (60 minutes rest in the supine position)
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SD1 and SD2 in ms
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At the baseline time (30 minutes rest in the supine position), during the warm-up (15 minutes in the treadmill) and immediately after the warm-up (60 minutes rest in the supine position)
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Perceived discomfort Scale (Likert-RFS)
Time Frame: At the baseline and Immediately after warm-up
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The degree of subjective discomfort reported by the participants in relation to the lower limbs refferd a blood flow restriction will be analyzed by Likert Scale of perception of effort of 0 to 10 points, 0 being "no discomfort" and 10 being "very discomfortable."
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At the baseline and Immediately after warm-up
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
March 15, 2024
Primary Completion (Actual)
August 20, 2024
Study Completion (Actual)
December 15, 2024
Study Registration Dates
First Submitted
August 11, 2022
First Submitted That Met QC Criteria
August 29, 2022
First Posted (Actual)
August 31, 2022
Study Record Updates
Last Update Posted (Actual)
May 31, 2025
Last Update Submitted That Met QC Criteria
May 27, 2025
Last Verified
May 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- Warm-up_BRF_FCT/UNESP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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