- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03149133
Comparison of Occlusive and Classical Hypertrophy Training in Terms of Thickness and Stiffness of The Muscle
August 16, 2017 updated by: ÖMER BATIN GÖZÜBÜYÜK, Istanbul University
Comparison of Occlusive and Classical Hypertrophy Training in Terms of Thickness and Stiffness of The Muscle, An Ultrasound-Based Study
Occlusive or ischemic training is a type of strength training which is becoming more and more popular every day.
The safety, efficacy and detailed description about the use of occlusive training is well documented in the literature.
However, the effects on hypertrophy and the stiffness of the muscle tissue are not studied.
We aimed to measure these changes by ultrasound technology in a randomized controlled design.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Patients were randomized into classical hypertrophy and occlusive hypertrophy groups.
The participants are free from any systemic disease, infection or recent injury.
Both groups perform hypertrophy training with different intensities.
The outcome measures are; thickness determined by B-mode ultrasound and stiffness by shear-wave elastography.
Comparison of both groups will be made.
Study Type
Interventional
Enrollment (Actual)
25
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
İstanbul, Turkey, 34093
- Istanbul University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Healthy recreational athletes
Exclusion Criteria:
- Any kind of systemic disorder
- Active or chronic infection
- Recent (last 6 months) musculoskeletal injury
- Performed strength training at last 72 hours
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Classical Hypertrophy
The classical hypertrophy group performs strength training with 75-80% of 1-Repetition Maximum.
|
Training with 75-80 % of 1-RM
|
Experimental: Occlusive Training
The occlusive hypertrophy group performs strength training with %35-50 of 1-Repetition Maximum.
|
Training with 35-50 % of 1-RM
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Thickness
Time Frame: 6 weeks
|
The thickness of the biceps brachii muscle determined by B-mode ultrasound
|
6 weeks
|
Stiffness
Time Frame: 6 weeks
|
The stiffness of the biceps brachii muscle determined by ultrasound elastography
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Strength change
Time Frame: 6 weeks
|
Arm flexion strength determined by isokinetic dynammometer
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 5, 2017
Primary Completion (Actual)
August 15, 2017
Study Completion (Actual)
August 16, 2017
Study Registration Dates
First Submitted
May 8, 2017
First Submitted That Met QC Criteria
May 9, 2017
First Posted (Actual)
May 11, 2017
Study Record Updates
Last Update Posted (Actual)
August 21, 2017
Last Update Submitted That Met QC Criteria
August 16, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2016/248
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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