PAPE Effect With Blood Flow Restriction and Push-Up Exercise (Post-Activation Performance Enhancement)
PAPE
Acute Effects of Push-Up Exercise Performed Under Varying Blood Flow Restriction Conditions on Upper Extremity Explosive Power Performance
1 other identifier
interventional
30
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2025
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
First Submitted
Initial submission to the registry
May 30, 2025
CompletedFirst Posted
Study publicly available on registry
June 11, 2025
CompletedStudy Start
First participant enrolled
June 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 20, 2025
CompletedNovember 18, 2025
November 1, 2025
2 months
May 30, 2025
November 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
throw distance
Seated unilateral medicine ball throw distance (in cm) -
will be measured immediately after the exercise protocol is completed three times at 4th, 8th, and 12th minutes
Secondary Outcomes (2)
Ball velocity (km/h)
will be measured by radar device after completion of the exercise three times at 4th, 8th, and 12th minutes
Rating of Perceived Exertion (RPE)
1 day (will be assessed at the end of the push-up exercise)
Study Arms (3)
Blood flow restriction exercise group
EXPERIMENTALParticipants 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.
Sham Blood flow restriction exercise group
PLACEBO COMPARATORIn 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.
Control group
ACTIVE COMPARATORParticipants perform push-up exercises without any cuff application. The same repetition and rest protocol is followed.
Interventions
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
Participants perform push-up exercises without any cuff application. The same repetition and rest protocol is followed
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
- +5 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul Faculty of Medicine
Istanbul, 34093, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Şensu Dinçer
Istanbul University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
May 30, 2025
First Posted
June 11, 2025
Study Start
June 20, 2025
Primary Completion
August 20, 2025
Study Completion
August 20, 2025
Last Updated
November 18, 2025
Record last verified: 2025-11