- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04755608
The Effect of Low-Intensity Resistance Exercise Training
The Effect OfF Low-Intensity Resistance Exercise Training Combined With Blood Flow Restruction On Triceps Brachii Muscle Volume And Performance
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Uskudar
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İstanbul, Uskudar, Turkey, 34668
- University and Health Sciences Physical Therapy and Rehabilitation
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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 Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Low Intensity Blood Flow Restriction Group
|
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.
|
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Active Comparator: High Intensity Resistant Training Group
|
People included in the study did resistance exercise with free weight at 70-80% of 1 MT.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
triceps muscle thickness
Time Frame: 6 weeks
|
Triceps brachial (TB) long head thickness was measured using the Esaote mylab C series ultrasound device.
|
6 weeks
|
|
triceps and biceps strength
Time Frame: 6 weeks
|
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
|
|
triceps and biceps endurance
Time Frame: 6 weeks
|
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
|
|
functional performances
Time Frame: 6 weeks
|
Upper Extremity Y Balance Test
|
6 weeks
|
|
delayed-onset muscle soreness
Time Frame: 6 weeks
|
Visual Analog Scale
|
6 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Yunus Emre Tütüneken, MSc, Istinye University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 46418926-19-138
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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