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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05452109
Other study ID # DrTez
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 12, 2022
Est. completion date October 27, 2023

Study information

Verified date June 2023
Source Biruni University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date October 27, 2023
Est. primary completion date April 27, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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.
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.

Locations

Country Name City State
Turkey Biruni University Istanbul
Turkey Istanbul University Cerrahpasa Istanbul

Sponsors (2)

Lead Sponsor Collaborator
Biruni University Istanbul University - Cerrahpasa (IUC)

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of Muscle Strength and Endurance Isokinetic dynamometer 6 weeks
Secondary Evaluation of Lower Extremity Power Vertical jump test 6 weeks
Secondary Evaluation of Aerobic Endurance Yo-Yo Intermittent Recovery Level 1 test 6 weeks
Secondary Evaluation of Change of Direction Speed T Test 6 weeks
Secondary Evaluation of Reactive Agility Y-Shaped Reactive Agility Test 6 weeks
Secondary Evaluation of Dynamic Balance Y Balance Test 6 weeks
Secondary Systemic Fatigue Lactate analysis 6 weeks
Secondary General Perceived Fatigue Borg scale 6 weeks
Secondary Evaluation of General Satisfaction and Perceived Performance Change 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". 6th week
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