- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07496944
Effects of Blood Flow Restriction and Small-Sided Games on Soccer Passing and Dribbling Stability Under Fatigue (BFR-SSG)
Effects of Blood Flow Restriction Combined With Small-Sided Games on Passing and Dribbling Stability of Soccer Players Under Fatigue
This study aims to investigate whether applying blood flow restriction (BFR) during small-sided soccer games (SSG) can help soccer players maintain their passing and dribbling stability when they are fatigued. The study includes 40 young male soccer players. Participants will be randomly divided into two groups:
One group will wear pressurized BFR cuffs on their legs (80% of limb occlusion pressure) during a 4v4 training game.
The other group will act as a control, wearing the same cuffs but without any pressure (0% pressure) during the exact same training game.Both groups will complete a 6-week training program, practicing 3 times a week. Before and after the 6-week period, researchers will test the players' physical and technical skills (such as jumping, passing, and dribbling). Importantly, these tests will be conducted both before and immediately after a tiring 45-minute exercise routine to see which training method is more effective at preventing performance drops caused by fatigue.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Beijing Municipality
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Beijing, Beijing Municipality, China, 100084
- China Football Institute, Beijing Sport University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Young male soccer players. Possess a systematic soccer specific training background and maintain a stable competitive state.
Cleared by the Physical Activity Readiness Questionnaire (PAR-Q), confirming that cardiovascular and metabolic systems can tolerate high-intensity physical testing and blood flow restriction interventions.
Exclusion Criteria:
- Any recent history of neuromuscular or musculoskeletal system injuries. Current smoking habit. Consumption of any sports nutrition supplements or drinks that could significantly affect muscle performance or neural excitability (e.g., creatine, caffeine, beta-alanine) within 3 months prior to the start of the study and throughout the experimental period.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Experimental: BFR-SSG Group
Participants are assigned to the blood flow restriction combined with small-sided games group.
They wear compression cuffs inflated to 80% of their individualized Limb Occlusion Pressure (LOP) during the core small-sided games training.
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The intervention lasts for 6 weeks, with 3 standardized 90-minute soccer training sessions per week.
During the core 20-minute intervention module, participants play 4v4 small-sided games (4 sets of 4 minutes, with 2 minutes of rest between sets).
Cuffs are inflated to 80% LOP during the exercise phase and fully deflated during the rest intervals.
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Sham Comparator: Sham Comparator: SSG Control Group
Participants are assigned to the control group.
They undergo the exact same small-sided games training while wearing identical cuffs that remain uninflated (0% LOP) to serve as a placebo.
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Participants complete the identical 6-week standardized soccer training program (3 sessions per week) and the 4v4 small-sided games module.
However, the cuffs worn by the participants remain at 0% LOP (uninflated) throughout the entire duration of the small-sided games.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Loughborough Soccer Passing Test (LSPT) Performance
Time Frame: Baseline (Week 0) and immediately post-intervention (Week 6). At both time points, the test is performed pre-fatigue and immediately post-fatigue.
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The LSPT assesses passing skill and stability.
The score is the total time (in seconds) required to complete 16 passes, plus penalty time added for passing errors.
To evaluate passing stability under fatigue, the performance attenuation rate is calculated by comparing scores obtained before and immediately after a standardized 45-minute fatigue-inducing protocol (Modified LIST).
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Baseline (Week 0) and immediately post-intervention (Week 6). At both time points, the test is performed pre-fatigue and immediately post-fatigue.
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20m Change-of-Direction Dribbling Test Technical Deficit
Time Frame: Baseline (Week 0) and immediately post-intervention (Week 6). At both time points, measured pre-fatigue and immediately post-fatigue.
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This test evaluates high-speed dribbling stability over a 20m slalom course.
The primary metric is the "technical deficit," calculated by subtracting the time taken to complete the course without the ball (sprint) from the time taken with the ball (dribbling).
This isolates technical stability from pure physical fatigue.
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Baseline (Week 0) and immediately post-intervention (Week 6). At both time points, measured pre-fatigue and immediately post-fatigue.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Countermovement Jump (CMJ) Height
Time Frame: Baseline (Week 0) and immediately post-intervention (Week 6). Measured pre-fatigue and immediately post-fatigue at both time points.
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Maximum vertical jump height (in centimeters) measured using a 3D force plate.
It evaluates the attenuation of lower limb neuromuscular function and explosive power under metabolic stress.
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Baseline (Week 0) and immediately post-intervention (Week 6). Measured pre-fatigue and immediately post-fatigue at both time points.
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Yo-Yo Intermittent Recovery Test Level 1 (YYIRT-1) Distance
Time Frame: Baseline (Week 0) and post-intervention (Week 6). Tests are conducted on a separate day, at least 48 hours apart from the main testing day, to avoid residual fatigu
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Total running distance (in meters) completed before exhaustion to assess chronic adaptations in soccer-specific intermittent endurance.
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Baseline (Week 0) and post-intervention (Week 6). Tests are conducted on a separate day, at least 48 hours apart from the main testing day, to avoid residual fatigu
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Creatine Kinase (CK) Concentration
Time Frame: Fasting baseline (Week 0), 24 hours after the first intervention session (Week 1), and 24 hours after the final intervention session (Week 6).
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Absolute creatine kinase concentration (U/L) measured from fingertip capillary blood to evaluate skeletal muscle micro-damage and chronic adaptation
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Fasting baseline (Week 0), 24 hours after the first intervention session (Week 1), and 24 hours after the final intervention session (Week 6).
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Collaborators and Investigators
Sponsor
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
- 2026027H
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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