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Completed

NCT Number: NCT07786129

Cluster Training With Blood Flow Restriction in Competitive 200-m Freestyle Swimmers

This study evaluated whether adding blood flow restriction (BFR) to cluster-based training could improve swimming performance and selected physiological responses in competitive swimmers. Twenty competitive swimmers were assigned using a matched, non-randomized design to either an experimental group performing cluster training combined with BFR or a control group performing the same cluster training without BFR. The intervention lasted 8 weeks, with five training sessions per week. The primary outcome was 200-m freestyle performance time. Secondary outcomes included serum concentrations of fibroblast growth factor-2 (FGF-2) and vascular endothelial growth factor-A (VEGF-A), standing long jump performance, mean 50-m split time during a 150-m swimming test, and repetitions completed during a cadence-controlled Burpee test. The study was designed to determine whether BFR provided additional performance and physiological benefits beyond cluster training alone.

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Key information

Age range

17 year–20 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Samarra Olympic Swimming Pool

Samarra, Muhafazat Salah ad Din, 34010, Iraq

About this study

Blood flow restriction (BFR) training is a training method in which pneumatic cuffs are applied proximally to the limbs to partially restrict vascular flow during exercise. Cluster training divides traditional exercise sets into smaller clusters of repetitions separated by short intra-set recovery periods. Combining these two approaches may increase the physiological stimulus of training while allowing repeated high-quality exercise efforts.

This controlled, non-randomized matched-intervention study included 20 competitive 200-m freestyle swimmers. Participants were matched according to baseline 200-m freestyle performance, sex, and standing long jump distance and were assigned to one of two groups. The experimental group completed cluster training combined with BFR, whereas the control group completed cluster training without BFR.

The training intervention lasted 8 weeks and consisted of five 90-minute training sessions per week. Sessions included a standardized warm-up, a main training component, and a cool-down. Overall cardiovascular training intensity was prescribed relative to individual maximal heart rate, and cluster-based resistance exercises incorporated short intra-set recovery intervals.

BFR was applied only in the experimental group during selected dry-land cluster exercises using pneumatic cuffs positioned proximally on the upper arms and thighs. The cuffs remained inflated during exercise execution and short intra-set recovery periods and were deflated during the main inter-set recovery periods.

The primary outcome was change in 200-m freestyle performance time from baseline to the end of the 8-week intervention. Secondary outcomes included serum FGF-2 and VEGF-A concentrations, standing long jump distance, mean 50-m split time during a maximal 150-m swimming test, and performance in a cadence-controlled Burpee test. Blood samples were collected under standardized resting conditions to assess serum FGF-2 and VEGF-A concentrations.

The main objective was to determine whether the addition of BFR to cluster training was associated with greater improvements in swimming performance, selected physical-performance outcomes, and serum angiogenesis-related biomarkers compared with cluster training alone.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Competitive 200-m freestyle swimmers aged 17-20 years. At least 2 years of structured swimming training experience. Free from musculoskeletal injury for at least 6 months before enrollment. No previous regular experience with blood flow restriction training. Willing and able to complete the 8-week training intervention and all study assessments.

Exclusion criteria

History of cardiovascular, metabolic, thrombotic, or other vascular conditions that could contraindicate blood flow restriction exercise.

Current use of medications known to affect vascular tone or blood coagulation. Musculoskeletal injury or medical condition preventing participation in maximal swimming or dry-land training.

Attendance below 85% of the scheduled intervention sessions.

Treatment and study plan

Cluster Training With Blood Flow Restriction

Behavioral

An 8-week cluster-training program performed five sessions per week, with blood flow restriction applied during selected dry-land cluster exercises using pneumatic cuffs positioned proximally on the upper arms and thighs.

Cluster Training Alone

Behavioral

An 8-week cluster-training program performed five sessions per week without blood flow restriction.

Primary outcomes

  1. Change in 200-m Freestyle Performance Time

    Time frame: Baseline and post-intervention at 8 weeks

    Performance was assessed during a maximal 200-m freestyle swim in a standard 50-m pool using an electronic timing system with a precision of 0.01 s. Lower values indicate faster performance. The primary outcome was the change in performance time from baseline to the end of the 8-week intervention.

Sponsors and collaborators

Lead sponsor

Saif Rasheed Ghanim

Other

Registry information

Official study title

Cluster Training With Blood Flow Restriction and 200-m Freestyle Performance, FGF-2, and VEGF-A Responses in Competitive Swimmers: A Matched Controlled Study

Acronym: BFR-CLUSTER-SW

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Aug 25, 2026
Registry last updated
Aug 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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