Effects Of Blood Flow Restriction Exercise Applications On Physical Fitness Parameters

Sponsor
Eastern Mediterranean University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05225129
Collaborator
(none)
32
1
2
7.4
4.3

Study Details

Study Description

Brief Summary

Aim: The aim of the study; during the non-race season, blood flow-restricted exercises applied in addition to routine training programs to determine the effects on physical fitness parameters and sportive motivation of male canoe athletes aged 18 and over and to compare the results between the groups.

Method: Male athletes aged 18 and over who are licensed and actively engaged in canoeing in Turkey will be included in the study. Subjects will be divided into two groups , training and control. The training group will be given blood flow restricted exercise for 8 weeks and resistance training equivalent to 30% of 1 maximum repetition. In the control group, 30% of 1 MT of resistance training will be applied for 8 weeks without blood flow restriction. Before and after, athletes will be evaluated with sport-specific performance tests, muscle thickness measurement with ultrasound, isokinetic measurement of hamstring and quadriceps muscles at a speed of 60°/sec and 300°/sec. In addition, the muscles of the athletes will be evaluated with dynamic muscular measurements.

Condition or Disease Intervention/Treatment Phase
  • Other: blood flow restriction exercise
N/A

Detailed Description

The first evaluation will be made before the 8-week training, and the second evaluation will be made at the end of the 8-week training. Both groups will be re-evaluated for follow-up at 6 and 12 months from the start of the study. In the 4th week, it is aimed to improve the exercise protocols by increasing the number of sets and repetitions in both groups.

The training will start with a 10-minute warm-up exercise on the static bike, and then stretching exercises will be applied. The athlete is dressed in the KAK apparatus and the pressure is given continuously so that it is on the device. In the 30-minute CAC exercise training, the athlete will complete the resistance exercises on the Leg Press, Leg Curl, Leg Calf Raise, Quadriceps Extension machines while attached to the device.

In the exercise prescription, which is planned as 3 sets of 10 repetitions, a rest period of 60 seconds will be given between sets. A 10-minute cool-down period will be added at the end of the training.

Study Design

Study Type:
Interventional
Actual Enrollment :
32 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects Of Blood Flow Restriction Exercise Applications On Physical Fitness Parameters and Sporting Motivation in Canoe Athletes
Actual Study Start Date :
Jan 17, 2022
Anticipated Primary Completion Date :
Jun 30, 2022
Anticipated Study Completion Date :
Aug 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Training Group

Resistance training will be applied to the training group, equivalent to 30% of 1 maximum repetition with blood flow restricted exercise for 8 weeks , 2 days in a week.

Other: blood flow restriction exercise
blood flow restricted exercise, resistance training will be applied, corresponding to 30% of 1 maximum repetition for 8 weeks, 2 days in a week
Other Names:
  • resistance exercise
  • No Intervention: Control Group

    Resistance training will be applied to the control group, equivalent to 30% of 1 maximum repetition without blood flow restriction for 8 weeks , 2 days in a week.

    Outcome Measures

    Primary Outcome Measures

    1. Changes in the sportive performance will be measured by ergometer [At the beginning and at the end of 8 weeks]

      Indoor ergometer will be used to determine the sportive performance changes of canoe athletes.

    2. Changes in muscle thickness will be measured by ultrasound [At the beginning and at the end of 8 weeks]

      The thickness measurements of the Rectus Femoris, Vastus Medialis Obliqus, Vastus Lateralis and Hamstring muscles and the area measurements of the rectus femoris and hamstring muscles will be measured by the sports physician.

    3. Quadriceps and Hamstring muscle strength, endurance, Ham/Quad ratio will be evaluated with an isokinetic dynamometer. [At the beginning and at the end of 8 weeks]

      Angular velocities; 60 degrees/sec, 300 degrees/sec will be measured bilaterally with the Biodex System 3. For 60 degrees / sec, the athlete will do 5 repetitions, and for 300 degrees / sec, the athlete will do 15-20 repetitions. Before both measurements, evaluation will begin after 3 rewarmings.

    4. In the Dynamic Measurement of Muscular Strength, a repetitive maximum method is used to measure the force with the dynamic method. [At the beginning and at the end of 8 weeks]

      It is performed with an appropriate starting weight close to but below the person's maximal lifting capacity for any muscle group. After the first repetition, the weight is lifted until the maximum lifting force is reached. It determines the maximum weight that athletes can lift at once in normal joint movement.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 30 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • 18 years of age or older

    • Being a licensed athlete for at least 2 years,

    • No history of orthopedic injury in the last 6 months

    • Athletes who have been doing resistance exercise for at least 5 years

    Exclusion Criteria:
    • Presence of disease that will cause endothelial dysfunction (hypertension, cardiovascular diseases, neurological diseases, atherosclerosis)

    • History of deep vein thrombosis and peripheral vascular disease

    • Presence of acute infection

    • Cancer cases

    • Having undergone a surgical operation due to trauma in the last 6 months

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Eastern Mediterranean University Famagusta Cyprus 99628

    Sponsors and Collaborators

    • Eastern Mediterranean University

    Investigators

    • Study Chair: Berkiye Kırmızıgil, Asst. Prof., Eastern Mediterranean University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Burçin Uğur Tosun, Principal Investigator, Eastern Mediterranean University
    ClinicalTrials.gov Identifier:
    NCT05225129
    Other Study ID Numbers:
    • 2021/12/31
    First Posted:
    Feb 4, 2022
    Last Update Posted:
    Jul 6, 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
    Keywords provided by Burçin Uğur Tosun, Principal Investigator, Eastern Mediterranean University

    Study Results

    No Results Posted as of Jul 6, 2022