Effect of Blood Flow Restriction on Football-Related Performance Parameters

Sponsor
Biruni University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05452109
Collaborator
Istanbul University-Cerrahpasa (Other)
22
2
2
14
11
0.8

Study Details

Study Description

Brief Summary

The blood flow restriction method can have similar or superior effects to high-intensity exercises even in a short duration, which can positively affect some performance parameters, can be applied with low-intensity load and cause hypertrophy in the muscle by providing high metabolic stress, facilitating muscle growth without significantly changing the total training dose. The aim of this study is to investigate whether adding the blood flow restriction method to the classical training program can be more effective than the classical training applied alone in the development of football-related performance parameters.

Condition or Disease Intervention/Treatment Phase
  • Other: Blood Flow Restriction
  • Other: Classical Training Alone
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
22 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Other
Official Title:
Improvement of Football-Related Performance Parameters: Application of Blood Flow Restrictive Exercise
Anticipated Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Blood Flow Restriction + Classical Training

Other: Blood Flow Restriction
Blood flow restriction with low load (30-50% 1RM) for 2 sessions in a week for 6 weeks during classical training will be applied.

Experimental: Classical Training Alone

Other: Classical Training Alone
Classical training same as Group 1with moderate to high load (70-90% 1RM) for 2 sessions in a week for 6 weeks will be applied without blood restriction.

Outcome Measures

Primary Outcome Measures

  1. Evaluation of Muscle Strength and Endurance [6 weeks]

    Isokinetic dynamometer

Secondary Outcome Measures

  1. Evaluation of Lower Extremity Power [6 weeks]

    Vertical jump test

  2. Evaluation of Aerobic Endurance [6 weeks]

    Yo-Yo Intermittent Recovery Level 1 test

  3. Evaluation of Change of Direction Speed [6 weeks]

    T Test

  4. Evaluation of Reactive Agility [6 weeks]

    Y-Shaped Reactive Agility Test

  5. Evaluation of Dynamic Balance [6 weeks]

    Y Balance Test

  6. Evaluation of Muscle Fatigue [6 weeks]

    Surface EMG

  7. Systemic Fatigue [6 weeks]

    Lactate analysis

  8. General Perceived Fatigue [6 weeks]

    Borg scale

  9. Evaluation of General Satisfaction and Perceived Performance Change [6th week]

    General satisfaction and the change in performance perceived by the participants will be evaluated with the 7 points Global Rating of Change Scale after the training program. According to the scale, it is expressed as "-3: I am much worse, -2: I am worse, -1: I am a little worse, 0: No change, 1: I am a little better, 2: I am better, 3: I am much better".

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 30 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Being a male between the ages of 18-30 years

  • Volunteer to participate in the study

  • Playing football in one of the clubs in Istanbul for at least 1 year

  • Being in the pre-season of the club

  • Absence of any ongoing musculoskeletal problems that limit exercising

Exclusion Criteria:
  • Having at least one of the contraindications preventing the application of blood flow restriction (Smoking, previous venous thromboembolism, risk of peripheral vascular disease (ankle-brachial index <0.9), coronary heart disease, hypertension, hemophilia, etc.).

  • History of sports injury in the last 6 months

  • Orthopedic lower extremity surgery in the last 1 year

  • Body mass index ≥ 30 kg/m2

Contacts and Locations

Locations

Site City State Country Postal Code
1 Biruni University Istanbul Turkey
2 Istanbul University Cerrahpasa Istanbul Turkey

Sponsors and Collaborators

  • Biruni University
  • Istanbul University-Cerrahpasa

Investigators

  • Study Chair: Ayse Zengin Alpözgen, PhD, Istanbul University-Cerrahpasa

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Begum Kara Kaya, Lecturer, Biruni University
ClinicalTrials.gov Identifier:
NCT05452109
Other Study ID Numbers:
  • DrTez
First Posted:
Jul 11, 2022
Last Update Posted:
Jul 11, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jul 11, 2022