- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05958056
Low Load Resistance Exercises With Blood Flow Restriction Versus High Load Resistance Exercises
August 15, 2023 updated by: Alia A. Alghwiri, University of Jordan
The Acute Effect of Low Load Resistance Exercises With Blood Flow Restriction Versus High Load Resistance Exercises on Growth Hormone and Blood Lactate
Practical blood flow restriction (PBFR) is a new technique of reducing the venous return using a band with a pressure that is applied using a perceived pressure scale.
The studies that investigate the acute effect of using PBFR and regular high intensity exercises on the level of growth hormone (GH) and blood lactate (BL) after lower extremity training in collegiate athletes are scarce.
Study Overview
Detailed Description
Practical blood flow restriction (PBFR) is a new technique of reducing the venous return using a band with a pressure that is applied using a perceived pressure scale.
The studies that investigate the acute effect of using PBFR and regular high intensity exercises on the level of growth hormone (GH) and blood lactate (BL) after lower extremity training in collegiate athletes are scarce.
Therefore, this study aimed to investigate the acute effect of a single session low load resistance exercises with PBFR compared to a high load resistance exercises without PBFR on the levels of GH and BL.
A convenience sample of collegiate athletes were allocated to either an experimental group that performed low resistance exercises with PBFR or a control group that performed high resistance exercises without PBFR.
The levels of GH and BL were examined in 3 time points: pre-training, immediate post-training, and 15 minutes post-training for both groups.
Analysis of Variance (ANOVA) was used to assess the main and interaction effects of the groups.
Study Type
Interventional
Enrollment (Actual)
22
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
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Amman, Jordan, 11942
- The University of Jordan
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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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Student collegiate athletes.
- Age of 18 years and older.
- Free from any cardiovascular or respiratory disorders and did not have any injuries during the previous 12 months.
Exclusion Criteria:
- Students who were taking any medications for chronic conditions.
- Student who were taking any supplements.
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Low load resistance exercises with Practical blood flow restriction (PBFR)
Participants in the experimental group performed one session of 30% 1RM with Practical blood flow restriction training.
The number of repetitions in every set was 15 times with PBFR.19 Participants in the experimental group used the elite band (occlusion training bands) for both thighs during the training session.
The width of the thigh band was 5cm, which would produce a pressure between 160-240 mmHg.
This pressure range is appropriate for most of the individuals who used PBFR.27
The perceived pressure scale (PPS) was used to estimate the appropriate pressure (7 out of 10) in training before performing the exercises.28,29
The blood flow restriction bands booklet was used30 along with previous studies to design the training session.
Participants removed the BFR band immediately after the end of the training session.
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The training session included leg curl and leg extension exercises with 4 sets each.
Participants started with leg extension exercise for 4 sets with a 30-second rest periods between the sets.
Then, participants took a rest for 60 seconds.
Afterward, participants performed leg curl exercise for 4 sets with a 30-second rest periods between the sets.
Exercises in each set were performed continuously (uninterrupted) with a speed of 2 seconds for each repetition and a medium exercise performance speed.
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Active Comparator: High resistance exercises
Participants in the control group performed one session of 80% 1RM without PBFR.
The number of repetitions in every set was 10 times.
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The training session included leg curl and leg extension exercises with 4 sets each.
Participants started with leg extension exercise for 4 sets with a 30-second rest periods between the sets.
Then, participants took a rest for 60 seconds.
Afterward, participants performed leg curl exercise for 4 sets with a 30-second rest periods between the sets.
Exercises in each set were performed continuously (uninterrupted) with a speed of 2 seconds for each repetition and a medium exercise performance speed.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Growth Hormone
Time Frame: Before intervention.
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Blood test of the level of growth hormone
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Before intervention.
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Growth Hormone
Time Frame: Immediately post intervention.
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Blood test of the level of growth hormone
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Immediately post intervention.
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Growth Hormone
Time Frame: 15 minutes after the end of intervention.
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Blood test of the level of growth hormone
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15 minutes after the end of intervention.
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Blood lactate
Time Frame: Before intervention.
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Blood test of the level of Blood lactate
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Before intervention.
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Blood lactate
Time Frame: Immediately post intervention.
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Blood test of the level of Blood lactate
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Immediately post intervention.
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Blood lactate
Time Frame: 15 minutes after the end of intervention.
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Blood test of the level of Blood lactate
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15 minutes after the end of intervention.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: Alia Alghwiri, PhD, The University of Jordan
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)
March 1, 2021
Primary Completion (Actual)
December 1, 2021
Study Completion (Actual)
July 1, 2022
Study Registration Dates
First Submitted
July 14, 2023
First Submitted That Met QC Criteria
July 14, 2023
First Posted (Actual)
July 24, 2023
Study Record Updates
Last Update Posted (Actual)
August 16, 2023
Last Update Submitted That Met QC Criteria
August 15, 2023
Last Verified
August 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 4/2019
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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