- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06746792
Low Load, High Gains: Blood Flow Restriction's Impact on Quadriceps Adaptations
March 3, 2025 updated by: Mustafa Şakir Akgül, Karabuk University
Low-load resistance exercise with blood flow restriction (BFR-RE) presents a compelling alternative to high-load resistance exercise (HL-RE), particularly in scenarios where high loads are not feasible due to various limitations.
Blood flow restriction exercise restricts blood flow to the working muscle, creating a state of ischemia.
A significant advantage of BFR-RE lies in its capacity to stimulate muscle hypertrophy and strength adaptations using light external loads (20-30% 1RM), comparable to those achieved with high-load (HL) training programs that employ 70-85% 1RM As a result, BFR training has been increasingly adopted in both athletic performance and rehabilitation settings over the past few decades.
Quadriceps strength and power are essential factors in both the advancement of athletic performance and the successful return to unrestricted sporting activity following injury.
The findings of Culvenor et al.'s review strongly suggest that weakened quadriceps strength is a significant risk factor for symptomatic and functional decline in the knee during both activities of daily living and sport-recreational activities.
Numerous electromyographic (EMG) findings suggest that single-joint and multijoint exercises elicit varying muscle activation patterns.
For instance, single-joint exercises targeting the quadriceps, such as leg extensions, demonstrate higher EMG amplitudes compared to multijoint lower-extremity exercises like leg presses and squats.
Resistance training, characterized by the application of high mechanical tension, remains the cornerstone for promoting muscle hypertrophy, So, research suggests that higher training intensities are associated with greater hypertrophy, up to a certain point.
While both light and heavy loads have been shown to elicit similar muscle growth when sets are taken to failure.
Studies have reported that high-repetition training with light loads leads to greater central fatigue.
Existing literature comparing the effects of BFR-RE and HL-RE primarily focuses on the some quadriceps and hamstring muscle group and its associated exercises.
However, none of these studies employed a training protocol in which sets were taken to or near failure.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
30
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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Karabuk, Turkey, 78000
- Karabuk University Faculty of Sports Sciences
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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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- keep healthy
- must be able to attend training regularly
Exclusion Criteria:
- smoking habit
- had orthopedic conditions that hindered lower-body resistance exercise, had hypertension (140/90 mm Hg), or had a BMI exceeding 30 kg/m2
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: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Muscle thickness
Muscular hypertrophy , or muscle growth, refers to an increase in muscle mass.
There are two types of muscular hypertrophy: myofibrillar, which is an increase in myofibrils, and sarcoplasmic, which is an increase in muscle glycogen storage.
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BFR-RE group performed bilateral leg extension exercises to volitional exhaustion (90 seconds rest between sets, 30% 1RM) with BFR cuffs applied at 60% of limb occlusion pressure.
Other Names:
The HL-RE group performed the same exercise to volitional exhaustion (90 seconds rest between sets, 70% 1RM) without BFR cuffs.
Other Names:
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Experimental: Muscle stiffness and strength
Muscle and tendon stiffness is defined as an internal resistance to changes in muscle and tendon shape caused by an external force.
Muscle strength production takes place with the help of the elastic behavior of the muscles and tendons
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BFR-RE group performed bilateral leg extension exercises to volitional exhaustion (90 seconds rest between sets, 30% 1RM) with BFR cuffs applied at 60% of limb occlusion pressure.
Other Names:
The HL-RE group performed the same exercise to volitional exhaustion (90 seconds rest between sets, 70% 1RM) without BFR cuffs.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Thigh Circumference
Time Frame: 2 day
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Measurement of thigh circumference was performed at a point 33% distal to the inguinal crease, precisely matching the intended cuff application site as verified by a trained investigator.
The inguinal crease-to-superior patellar pole distance was also recorded using a standard anthropometric tape measure
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2 day
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Muscle Strength Test
Time Frame: 2 day
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Prior to commencing the strength assessment, using a Lafayette Manual Muscle Testing System (Lafayette Instrument Company, Lafayette®) a period of familiarization was allowed between the examiner and participant.
Subsequently, a trained examiner guided the participant through a series of practice repetitions of leg flexion, and leg extension movements until correct execution was confirmed.
The order of movements was randomized.
The participant was then verbally instructed to perform three maximal contractions for each movement (3-second hold).
A 1-minute rest interval was incorporated between successive contractions, and a 3-minute rest interval was implemented between different movement sets.
Measurement of leg extension were obtained with participants in a seated position, while leg flexion measurement were taken with participants in a prone position.
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2 day
|
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Muscle Thickness Assessment
Time Frame: 4 day
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Subjects had not engaged in physical activity before the study (48-72 hours), and muscle thickness (MT) was measured at a prone rest position.
All muscle thickness measurements were obtained with a single ultrasound device equipped with a 2-9 MHz linear transducer.
A researcher (medical doctor, N.K.K) who was blinded to the exercise groups with more than 10 years of experience in musculoskeletal imaging performed all measurement
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4 day
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Muscle Stiffness and Shear Wave Elastography
Time Frame: 4 day
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After the muscle thickness measurements, the stiffness measurements of quadriceps muscle were obtained using the shear wave elastography (SWE) imaging option of the same ultrasound device with the same linear transducer.
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4 day
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Anthropometric Measurements
Time Frame: One day
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Height, weight and Body mass index (BMI) were measured using a stadiometer (InBody 270 (Biospace, California, USA), with subjects wearing light clothing and no shoes.
Measurements were taken before the exercise program.
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One day
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Blood Pressure
Time Frame: One day
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After a 5-minute supine rest, participants' left brachial blood pressure (BP) was measured twice (1-minute interval).
The average of the two closest readings (within 5 mmHg) was recorded in mmHg
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One day
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Heart Rate
Time Frame: One day
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After a 5-minute supine rest
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One day
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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)
October 11, 2024
Primary Completion (Estimated)
March 29, 2025
Study Completion (Estimated)
March 29, 2025
Study Registration Dates
First Submitted
December 11, 2024
First Submitted That Met QC Criteria
December 20, 2024
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 3, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- KarabukUniSportsSciences
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
All antropometric and muscle strength, muscle thickness, and muscle stiffness parameters will be shared
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
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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