Effects of Blood Flow Restriction and Small-Sided Games on Soccer Passing and Dribbling Stability Under Fatigue
BFR-SSG
1 other identifier
interventional
40
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 20, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 10, 2026
CompletedFirst Submitted
Initial submission to the registry
March 22, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 22, 2026
CompletedFirst Posted
Study publicly available on registry
March 27, 2026
CompletedMarch 27, 2026
March 1, 2026
2 months
March 22, 2026
March 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Loughborough Soccer Passing Test (LSPT) Performance
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).
Baseline (Week 0) and immediately post-intervention (Week 6). At both time points, the test is performed pre-fatigue and immediately post-fatigue.
20m Change-of-Direction Dribbling Test Technical Deficit
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.
Baseline (Week 0) and immediately post-intervention (Week 6). At both time points, measured pre-fatigue and immediately post-fatigue.
Secondary Outcomes (3)
Countermovement Jump (CMJ) Height
Baseline (Week 0) and immediately post-intervention (Week 6). Measured pre-fatigue and immediately post-fatigue at both time points.
Yo-Yo Intermittent Recovery Test Level 1 (YYIRT-1) Distance
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
Creatine Kinase (CK) Concentration
Fasting baseline (Week 0), 24 hours after the first intervention session (Week 1), and 24 hours after the final intervention session (Week 6).
Study Arms (2)
Experimental: BFR-SSG Group
EXPERIMENTALParticipants 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.
Sham Comparator: SSG Control Group
SHAM COMPARATORParticipants 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.
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
China Football Institute, Beijing Sport University
Beijing, Beijing Municipality, 100084, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- Randomization and group allocation were performed by an independent researcher not involved in data collection or analysis. Group assignments were hidden using coding to ensure that the investigators and outcome assessors remained completely blinded to the intervention conditions throughout the entire study process.
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Graduate Student
Study Record Dates
First Submitted
March 22, 2026
First Posted
March 27, 2026
Study Start
January 20, 2026
Primary Completion
March 10, 2026
Study Completion
March 22, 2026
Last Updated
March 27, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to participant confidentiality and institutional data protectionpolicies.