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PAPE Effect With Blood Flow Restriction and Push-Up Exercise (Post-Activation Performance Enhancement)

I

Istanbul University

Status

Enrolling

Conditions

Blood Flow Restriction Exercise

Treatments

Other: Sham blood flow restriction exercise
Other: Control group
Other: Blood flow restriction exercise group

Study type

Interventional

Funder types

Other

Identifiers

NCT07015515
PAPE-BFR-2025

Details and patient eligibility

About

This study aims to compare the acute effects of push-up exercises performed under different blood flow restriction (BFR) conditions on upper extremity explosive strength performance, measured via the seated unilateral medicine ball throw test.

Full description

The study includes three push-up conditions (BFR, sham BFR, and no BFR). Performance is evaluated via medicine ball throws at the 4th, 8th, and 12th minutes post-exercise. Exercises are applied in a crossover design with 50% limb occlusion pressure (LOP) BFR, sham, and control arms. Throw distance and ball velocity (measured by radar device) are primary outcomes. RPE scale is used to assess perceived exertion.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being between 18 and 25 years old
  • Being a volleyball player
  • Having trained regularly in the last 6 months
  • Ability to perform at least 5 repetitions of push-up with own body weight
  • Voluntarily agreeing to participate and signing the informed consent form

Exclusion criteria

  • History of shoulder or upper extremity injury requiring physical therapy or surgery
  • History of venous thromboembolism
  • Hematological disorders
  • Coronary artery disease
  • Peripheral arterial disease
  • Hypertension (systolic/diastolic > 140 mmHg/90 mmHg)
  • History or high risk of deep vein thrombosis
  • Blood clotting disorders
  • Poor circulation
  • Inadequate lymphatic system
  • History of endothelial dysfunction
  • Varicose veins
  • Peripheral vascular disease
  • Diabetes
  • Easy bruising
  • Active infection
  • Cancer
  • Renal failure
  • Pregnancy
  • Intolerance to intervention

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

30 participants in 3 patient groups, including a placebo group

Blood flow restriction exercise group
Experimental group
Description:
Participants will perform push-up exercises with 50% arterial occlusion pressure applied to their dominant arm. The cuff is inflated before the exercise and maintained throughout 3 sets of 5 repetitions. There is a 2-minute rest between sets.
Treatment:
Other: Blood flow restriction exercise group
Sham Blood flow restriction exercise group
Placebo Comparator group
Description:
In this group, a BFR cuff will be placed on the upper extremity in the same location as in the real BFR group. During the application, the participant will be led to believe that the cuff is being inflated, although no actual pressure will be applied. The participant will see the cuff being wrapped and apparently inflated, but there will be no physical pressure restricting circulation during the exercise. This aims to control the psychological effects (e.g., the belief that "something is being applied") on performance.
Treatment:
Other: Sham blood flow restriction exercise
Control group
Active Comparator group
Description:
Participants perform push-up exercises without any cuff application. The same repetition and rest protocol is followed.
Treatment:
Other: Control group

Trial contacts and locations

1

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Central trial contact

Sena Aktürk, MSc. Student; Şensu Dinçer, Assist.Prof

Data sourced from clinicaltrials.gov

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