BFR Rope Training in Male Volleyball Players

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18-25
SponsorKarabuk University

About this trial

The study will be conducted during the preparatory period of the volleyball players and will span eight weeks. Throughout this period, athletes will continue their regular volleyball training four days per week, while the experimental group (n = 10) will perform rope training with blood flow restriction (BFR) twice per week, and the control group (n = 10) will perform the same rope training without BFR. Assessments will be carried out at the beginning of the 8-week period (pre-test) and at the end of the intervention (post-test). For both groups, all exercises will target the upper-extremity muscle groups. During the study, participants will be instructed to avoid consuming any medications, engaging in additional strenuous physical activities, and using any techniques or ergogenic aids that might influence the results. In both testing sessions, a standardized warm-up protocol will be implemented, consisting of a 5-minute treadmill run at 9 km/h on a Sprint Runner device (Hoggan Health Industries, Draper, UT), followed by 3 minutes of light full-body stretching. This warm-up procedure will be applied consistently across both groups to ensure standardization.

Eligibility criteria

Qualifiers

Being healthy

Male volleyball athletes

Willing to maintain the intervention for all sessions

Disqualifiers

Being under 18 years old

Having a chronic disease

Contraindications for exercise

Trial design

Treatments tested in this trial

  • Blood Pressure
  • Muscle Strength
  • Serve Speed
  • Blood Flow Restriction
  • Rating of Perceived Exertion
  • Battle Rope Training
  • Arm Circumference
  • Skeletal Muscle Endurance
  • Anaerobic Power
  • Bench Press 1RM Test
  • Triceps Push-Down 1RM Test
  • Hand Grip Strength Test
  • Yo-Yo IR1 Test
  • Ultrasound (US)
  • Perceived Discomfort Level
  • Exercise Enjoyment
  • Perceived Exertion Level (OMNI-RES)

Treatment groups

26 Participants
are divided into 17 treatment groups

17

Treatment groups

See each treatment group below.

Sponsors and collaborators