NCT07786597

Brief Summary

The purpose of this study was to investigate the effects of practical blood flow restriction (pBFR) applied during swimming training on sprint and endurance performance in master swimmers. Fifty-four male master swimmers (36-51 years) were randomly assigned to either a pBFR group (n = 27) or a control group (n = 27). Both groups followed the same swimming training programme twice weekly for eight weeks. In the pBFR group, elastic bands were applied to the proximal region of both thighs at a perceived tightness level of 7/10 during approximately 20 min of low-intensity swimming performed at the beginning of each training session. Performance was assessed using a 50-m freestyle kick test, a 100-m freestyle swimming test, and a 12-min Cooper swimming test.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
54

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2024

Geographic Reach
1 country

1 active site

Status
completed

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

February 8, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 10, 2024

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 5, 2025

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

August 20, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 26, 2026

Completed
Last Updated

August 26, 2026

Status Verified

August 1, 2026

Enrollment Period

4 months

First QC Date

August 20, 2026

Last Update Submit

August 25, 2026

Conditions

Keywords

Practical blood flow restriction (pBFR)swimming performancemaster swimmers

Outcome Measures

Primary Outcomes (3)

  • Cooper 12-Minute Swimming Test

    Cooper 12-Minute Swimming Test Swimmers were asked to swim continuously in freestyle for 12 minutes, covering the maximum possible distance. The test began with a push-off from the pool wall, and turns were performed using the appropriate technique. Participants were informed to stop immediately if they would experience symptoms such as shortness of breath or inability to continue swimming. The total distance covered in 12 minutes was recorded in meters.

    Pre-intervention and post-intervention at 8 weeks

  • Short-distance kicking performance test

    Swimmers completed the test distance using only leg kicks while holding a kickboard, without performing arm strokes. This sprint test was designed to assess the propulsive force generated by the lower limbs. The test started with a push-off from the pool wall, and turns were executed by pushing off the wall. Time was recorded in seconds.

    Baseline and 8 weeks

  • 100 m Freestyle Swimming Test

    The test began with a dive start and included turns performed according to FINA rules. Swimming time was recorded using three independent stopwatches, and the mean value of the three measurements was used for statistical analysis.

    Baseline and 8 weeks

Study Arms (2)

Experimental Group

EXPERIMENTAL

Blood Flow Restriction Swimming Training

Device: Practical Blood Flow Restriction Bands

Control Group

ACTIVE COMPARATOR

No Intervention

Other: Traditional Swimming Training

Interventions

Practical blood flow restriction was applied during swimming training using elastic bands on the proximal thighs.

Experimental Group

Participants in the control group performed standard swimming training without blood flow restriction.

Control Group

Eligibility Criteria

Age36 Years - 51 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • \* Voluntary participation with signed written informed consent

You may not qualify if:

  • \* History of hypertension, diabetes, or cardiovascular disease
  • History of deep vein thrombosis or pulmonary embolism
  • Neurological disorders or rheumatic diseases
  • Obesity or any other chronic condition
  • Sports-related injury within the previous 6 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul University - Cerrahpasa

Istanbul, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

August 20, 2026

First Posted

August 26, 2026

Study Start

February 8, 2024

Primary Completion

June 10, 2024

Study Completion

March 5, 2025

Last Updated

August 26, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Locations