ClinicalTrials.gg
CompletedNCT07786129BFR-CLUSTER-SWUpdated Oct 16, 2026

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

An interventional study of Cluster Training With Blood Flow Restriction and Cluster Training Alone in Athletic Performance and Exercise Training, sponsored by Saif Rasheed Ghanim. Completed at 1 site in Iraq. Open to participants aged 17 Years to 20 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-16.

Sponsored by Saif Rasheed Ghanim · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Jan 2026, registered Aug 2026).
Updated Oct 16, 2026Primary completion movedStudy completion moved+1 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Non-randomized
Ages
17 Years to 20 Years
Sex
All
01

Study summary

This study evaluated the effects of adding individualized blood flow restriction (BFR) to cluster resistance training on swimming performance, physical fitness, and selected circulating growth factors in competitive swimmers.

Forty competitive swimmers participated in a matched, non-randomized controlled intervention involving two groups (20 participants per group). The experimental group performed cluster resistance training combined with individualized BFR, whereas the control group completed the same training program without BFR.

The intervention lasted 10 weeks, comprising five supervised training sessions per week (50 sessions in total). Each 100-minute session included a 15-minute warm-up, 30 minutes of dry-land cluster resistance training, 50 minutes of swimming-specific training, and a 5-minute cool-down.

Dry-land resistance exercises were performed at 60-70% of one-repetition maximum (1RM). BFR pressure was individualized to 50% of arterial occlusion pressure (AOP) for the upper limbs and 60% for the lower limbs. Swimming training intensity was prescribed according to individual maximal heart rate (HRmax).

The primary outcome was the change in 200-m freestyle swimming performance time from baseline to the end of the 10-week intervention. Secondary outcomes included standing long jump performance, mean 50-m split time during a continuous maximal 150-m swim, cadence-controlled Burpee repetitions, and resting serum concentrations of fibroblast growth factor-2 (FGF-2) and vascular endothelial growth factor A (VEGF-A).

The study investigated whether individualized BFR combined with cluster resistance training was associated with greater improvements in swimming performance and physiological responses compared with cluster resistance training alone.

Read the detailed description

Blood flow restriction (BFR) training involves the application of pneumatic cuffs to the proximal regions of the limbs to partially restrict arterial inflow and venous return during exercise. Cluster resistance training incorporates brief recovery intervals between small groups of repetitions to reduce fatigue and maintain exercise performance.

This matched, non-randomized controlled study investigated the effects of combining individualized BFR with cluster resistance training on swimming performance, physical fitness, and circulating growth factors in competitive swimmers.

Forty competitive swimmers aged 17-20 years participated in the study. Participants were matched according to sex, baseline 200-m freestyle performance, and standing long jump distance and allocated to two parallel groups: an experimental group (n = 20) performing cluster resistance training with individualized BFR and a control group (n = 20) performing the same training program without BFR.

The intervention lasted 10 weeks, comprising five supervised training sessions per week (50 sessions in total). Each session lasted 100 minutes, consisting of a 15-minute warm-up, an 80-minute main training phase, and a 5-minute cool-down. The main phase included 30 minutes of dry-land cluster resistance training followed by 50 minutes of swimming-specific training.

Dry-land resistance exercises were prescribed at 60-70% of one-repetition maximum (1RM). The experimental group performed the resistance exercises with individualized BFR pressures corresponding to 50% of arterial occlusion pressure (AOP) for the upper limbs and 60% for the lower limbs. The control group performed the same exercises without BFR.

Swimming training intensity was prescribed relative to individually assessed maximal heart rate (HRmax). Weekly intensity targets progressed through 60%, 70%, 75%, 85%, 65%, 80%, 90%, 95%, 100%, and 80% of HRmax across the 10-week intervention. These percentages represented prescribed intensity targets rather than intensities maintained continuously throughout each session.

Swimming performance was assessed using a maximal 200-m freestyle test in a standardized 50-m swimming pool with electronic timing. Additional performance assessments included standing long jump distance, mean 50-m split time during a continuous maximal 150-m swim, and repetitions completed during a cadence-controlled Burpee test.

Resting serum concentrations of fibroblast growth factor-2 (FGF-2) and vascular endothelial growth factor A (VEGF-A) were assessed using enzyme-linked immunosorbent assays (ELISA). Post-intervention blood samples were collected under standardized fasting conditions 48 hours after the final training session.

The primary outcome was the change in 200-m freestyle performance time from baseline to Week 10. Secondary outcomes included changes in physical-performance measures and resting serum FGF-2 and VEGF-A concentrations.

The study evaluated whether adding individualized BFR to cluster resistance training was associated with greater improvements in swimming performance and selected physiological responses compared with cluster resistance training alone.

02

Conditions studied

  • Athletic Performance
  • Exercise Training

Keywords

  • Blood Flow Restriction
  • Cluster Training
  • Competitive Swimming
  • 200-m Freestyle
  • FGF-2
  • VEGF-A
03

In context

Lead sponsor

Saif Rasheed Ghanim is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
17 Years to 20 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    Cluster Training With Blood Flow Restriction

    Participants in this arm completed an 8-week cluster-training program combined with blood flow restriction (BFR). Training was performed five sessions per week. Pneumatic cuffs were applied proximally to the upper arms and thighs during selected dry-land cluster exercises and intra-set recovery periods, and were deflated during the main inter-set recovery periods.

    Behavioral: Cluster Training With Blood Flow Restriction

  • Active comparator
    Cluster Training Alone

    Participants in this arm completed the same 8-week cluster-training program and overall training schedule as the experimental group, but without blood flow restriction. Training was performed five sessions per week.

    Behavioral: Cluster Training Alone

Interventions

  • BehavioralCluster Training With Blood Flow Restriction

    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.

  • BehavioralCluster Training Alone

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

06

What researchers measure

Primary outcomes

  1. Change in 200-m Freestyle Performance Time

    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 10-week intervention.

    Time frame: Baseline (Week 0) and post-intervention (Week 10)

07

Study locations

1 site
  • Samarra Olympic Swimming Pool
    Samarra, Muhafazat Salah ad Din 34010, Iraq
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it moved

Ran from Jan 2026 to primary completion in Apr 2026, 3 months.

Since we started tracking on Sep 25, 2026, the dates moved once, on Oct 16, 2026: primary completion Mar 2026 → Apr 2026 and completion Jun 2026 → Apr 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Aug 21, 2026
First posted
Aug 25, 2026
StartActual
Jan 15, 2026
Primary completionActual
Apr 19, 2026was Mar 2026
CompletionActual
Apr 26, 2026was Jun 2026
Last update
Oct 16, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Primary completion
Mar 19, 2026→Apr 19, 2026
Oct 16, 2026
Study completion
Jun 15, 2026→Apr 26, 2026
Oct 16, 2026
Primary outcomes
1 time frame changed, 1 description edited
What changed in the outcomes
  • Time frameChange in 200-m Freestyle Performance TimeBaseline and post-intervention at 8 weeks → Baseline (Week 0) and post-intervention (Week 10)
  • DescriptionChange in 200-m Freestyle Performance Time: how it is measured was reworded
Oct 16, 2026
Show all 1 update
  1. Oct 16, 2026
    Primary completion Mar 19, 2026→Apr 19, 2026
    Study completion Jun 15, 2026→Apr 26, 2026
    Primary outcomes 1 time frame changed, 1 description edited
    What changed in the outcomes
    • Time frameChange in 200-m Freestyle Performance TimeBaseline and post-intervention at 8 weeks → Baseline (Week 0) and post-intervention (Week 10)
    • DescriptionChange in 200-m Freestyle Performance Time: how it is measured was reworded
    + 2 other changes: verification date and description

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07786129
Lead sponsor
Saif Rasheed Ghanim
Responsible party
Saif Rasheed Ghanim (Assistant Professor of Exercise Physiology, Samarra University) — Sponsor-investigator
First posted
Aug 25, 2026
Start date
Jan 15, 2026
Primary completion
Apr 19, 2026
Completion
Apr 26, 2026
Last update
Oct 16, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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