- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06912867
Effects of BFR Training on Muscle Strength, Thickness, and Motivation in National Adolescent Male Canoe Athletes (BRAVE-CAN)
The BRAVE-CAN Study: A Clinical Trial Investigating the Effects of Blood Flow Restriction Training on Lower Extremity Muscle Strength, Muscle Thickness, and Sport Motivation in Adolescent Male National Canoe Athletes
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This randomized controlled trial aims to investigate the physiological and psychological effects of blood flow restriction (BFR) training on adolescent elite male canoe athletes. Canoeing is a demanding endurance sport requiring well-developed upper and lower extremity strength, core stability, and high levels of sport-specific motivation. In adolescent athletes, whose musculoskeletal and hormonal systems are still developing, traditional high-load resistance training may not always be feasible or safe. BFR training, which involves restricting venous blood flow while performing low-intensity exercises, has emerged as a potential alternative for promoting muscle hypertrophy and strength with reduced mechanical stress.
In this study, a total of 40 adolescent male canoe athletes aged 15 to 18 years are enrolled and randomized into two groups: a BFR intervention group (n=28) and a control group (n=12). The intervention group participates in a supervised BFR-supported resistance training program twice a week for 8 weeks using KAATSU C3 equipment applied to the lower limbs. Both groups continue their regular canoe training programs. Assessments are performed before and after the 8-week training period by blinded evaluators.
Primary outcome measures include isokinetic muscle strength tests, ultrasound-based measurements of muscle thickness and cross-sectional area (CSA), and scores from the validated Sport Motivation Scale. The study is designed to explore potential effects of BFR training on muscular strength, hypertrophy, sprint capacity, and motivational subdomains in this athletic population.
This research aims to contribute to the growing body of literature regarding the applicability of BFR training in adolescent athletes, with a focus on its physiological and psychological outcomes. Findings from this study may help inform future training strategies for youth involved in high-performance sports.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Famagusta, Cyprus, 99010
- Burcin Ugur Tosun
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male athletes aged between 15 and 18 years
- Registered elite-level canoe athletes actively training within a national program
- Minimum of 2 years of canoe sport experience
- Voluntary participation with informed consent (for minors: parental/guardian consent)
- Medically cleared to participate in physical training and testing
Exclusion Criteria:
- Existing orthopedic injuries or musculoskeletal disorders affecting lower extremities
- History of cardiovascular, neurological, or metabolic diseases
- Non-compliance with the training protocol during the study
- Participation in any other structured strength training program during the study period
- Use of medications or supplements affecting muscle performance or motivation
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: BFR Training Group
Participants performed supervised low-load resistance training with BFR using KAATSU C3 equipment twice a week for 8 weeks.
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Participants performed supervised low-load resistance training with BFR using KAATSU C3 equipment twice a week for 8 weeks.
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No Intervention: Control Group
Participants in this group continued their standard canoe training program without additional blood flow restriction exercises.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lower Extremity Muscle Strength (Peak Torque, Nm) - measured via isokinetic dynamometry
Time Frame: Baseline (Week 0) and Post-intervention (Week 8)
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Muscle strength of the quadriceps and hamstring muscles was assessed using an isokinetic dynamometer (Biodex System 4) at angular velocities of 60°/s and 300°/s.
Peak torque (in Newton-meters) was recorded for both right and left lower limbs.
Measurements were conducted at baseline and after the 8-week intervention period by a blinded physiotherapist.
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Baseline (Week 0) and Post-intervention (Week 8)
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Muscle Thickness (mm) - measured via ultrasound
Time Frame: Baseline (Week 0) and Post-intervention (Week 8)
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Muscle thickness and cross-sectional area of the quadriceps femoris and hamstring muscle groups were evaluated using B-mode ultrasound imaging (Mindray DP-10).
Measurements were taken bilaterally from standardized anatomical landmarks in a resting position.
The assessment was performed by a blinded sports medicine physician at baseline and after 8 weeks of training.
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Baseline (Week 0) and Post-intervention (Week 8)
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Sport-Specific Motivation Score - measured using the Sport Motivation Scale (validated Turkish version)
Time Frame: Baseline (Week 0) and Post-intervention (Week 8)
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Sport-specific motivation levels will be assessed using the Turkish-validated version of the Sport Motivation Scale-II. The scale consists of 18 items rated on a 7-point Likert scale ranging from 1 (Does not correspond at all) to 7 (Corresponds exactly). Total scores range from 18 to 126, with higher scores indicating greater overall sport motivation. The scale includes three subdimensions relevant to this study: Motivation to Show Strength Motivation to Approach Success Motivation to Avoid Failure Subscale scores are calculated as the mean of related items. Higher subscale scores indicate a stronger level of that specific motivational trait. |
Baseline (Week 0) and Post-intervention (Week 8)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: burcin ugur tosun, PHD, "Bandırma Onyedi Eylül University, Faculty of Health Sciences"
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025-43
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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