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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04755608
Other study ID # 46418926-19-138
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2019
Est. completion date August 1, 2020

Study information

Verified date February 2021
Source Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It was to compare the effect of low-load resistance training with blood flow restriction (LL-BFR) and high-intensity resistance training (HI-RT) on muscle strength, endurance and volume, functional performance, and delayed onset muscle soreness (DOMS). The study included 13 young women. It is a controlled study designed for individuals to perform two different exercise protocols unilaterally. The persons were randomly allocated into two groups as LI- BFR (Group I, n = 13) and HI-RT (Group II, n = 13). Both groups received training for 6 weeks and 3 days a week. Blood flow restriction was performed only in group I.


Description:

Both sides triceps muscle thickness, triceps and biceps strength and endurance, functional performances (upper extremity Y balance test (UQYBT)), delayed-onset muscle soreness (DOMS) were evaluated before and after training.


Recruitment information / eligibility

Status Completed
Enrollment 13
Est. completion date August 1, 2020
Est. primary completion date August 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 26 Years
Eligibility Inclusion Criteria: - Between the ages of 18-26, - Do not have a chronic disease history and do not use medication, - Female individuals were included. Exclusion Criteria: - People who made resisted exercise in the last 6 months, - Smoker, - BMI above 30 kg / m2, - Individuals with hypertension were excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Low Intensity Exercises with Blood Flow Restriction
In the exercise protocol, people exercised resistance between 20% and 30% of 1 MaxRepetition with free weight. In addition, blood flow was restricted in 70% of the arterial occlusion pressure of the individual with the help of a cuff during exercise.
High Intensity Resistant Exercise
People included in the study did resistance exercise with free weight at 70-80% of 1 MT.

Locations

Country Name City State
Turkey University and Health Sciences Physical Therapy and Rehabilitation Istanbul Uskudar

Sponsors (1)

Lead Sponsor Collaborator
Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary triceps muscle thickness Triceps brachial (TB) long head thickness was measured using the Esaote mylab C series ultrasound device. 6 weeks
Primary triceps and biceps strength Triceps brachial muscle strength was evaluated with an isokinetic dynamometer (Cybex HUMAC / NORM, CSMI, 2004). Isometric muscle strength measurement was performed at the beginning and end of the study at angular velocities of 0-150 ° elbow range, 60 ° / s (strength measurement) 6 weeks
Primary triceps and biceps endurance Triceps brachial muscle strength was evaluated with an isokinetic dynamometer (Cybex HUMAC / NORM, CSMI, 2004). Isometric muscle strength measurement was performed at the beginning and end of the study at angular velocities of 0-150 ° elbow range, 180 ° / s (endurance measurement). 6 weeks
Primary functional performances Upper Extremity Y Balance Test 6 weeks
Primary delayed-onset muscle soreness Visual Analog Scale 6 weeks
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