- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05710757
Investigating Proximal Muscle Strength Effects by Incorporating Proximal Muscle Lengthening
March 19, 2024 updated by: LaToya Green, University of Tennessee
The purpose of this study is to assess strength gains of proximal musculature in the nondominant upper extremity after implementing blood flow restriction (BFR) and myofascial release (MFR) with the supplementation of whey protein.
Study Overview
Status
Active, not recruiting
Intervention / Treatment
Detailed Description
The purpose of this study is to assess strength gains of proximal musculature in the nondominant upper extremity after implementing blood flow restriction (BFR) and myofascial release (MFR) with the supplementation of whey protein.
Blood flow restricted (BFR) exercise is the brief and non-continuous blockage of venous blood flow using a device that restricts the flow of blood while exercising.
This technique is used to produce hypertrophy (muscle growth) and strength responses while exercising at a lighter load than traditionally required to produce a similar response.
Myofascial release (MFR) is a technique that involves applying gentle sustained pressure into the myofascial connective tissue restrictions to eliminate pain and restore motion.
Study Type
Interventional
Enrollment (Estimated)
60
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 Contact
- Name: LaToya L Green, EdD
- Phone Number: 901-448-5888
- Email: lgreen24@uthsc.edu
Study Contact Backup
- Name: Myra M Meekins, PhD
- Phone Number: 901-448-5888
- Email: mmeekins@uthsc.edu
Study Locations
-
-
Tennessee
-
Memphis, Tennessee, United States, 38163
- University of Tennessee Health Science Center
-
Contact:
- Kimberly Williams, MS
- Phone Number: 901-448-1343
- Email: kwilli72@uthsc.edu
-
Contact:
- Jessica McMorris, MS
- Phone Number: 901.448.5920
- Email: jmcmorr1@uthsc.edu
-
Principal Investigator:
- LaToya L Green, EdD
-
Sub-Investigator:
- Myra M Meekins, PhD
-
-
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 30 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Healthy individuals between the age of 18 and 30
Exclusion Criteria:
- Individuals with uncontrolled high blood pressure
- Individuals with sickle cell anemia, current pregnancy
- Individuals with a history of deep vein thrombosis
- Individuals with diabetes
- Individuals with active infection
- Individuals with less than normal range of motion or muscle strength
- Individuals with moderate to severe upper extremity injury in the past 12 months
- Individuals with a current diagnosis of cancer.
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Myofascial Release
The Experimental group will receive a myofascial release pectoralis minor release intervention.
|
Myofascial release (MFR) is a technique that involves applying gentle sustained pressure into the myofascial connective tissue restrictions to eliminate pain and restore motion.
Blood flow restricted (BFR) exercise is the brief and non-continuous blockage of venous blood flow using a device that restricts the flow of blood while exercising.
This technique is used to produce hypertrophy (muscle growth) and strength responses while exercising at a lighter load than traditionally required to produce a similar response.
Sham MFR.
|
Sham Comparator: Sham Myofascial Release
The Control group will receive a sham myofascial release pectoralis minor release intervention.
|
Myofascial release (MFR) is a technique that involves applying gentle sustained pressure into the myofascial connective tissue restrictions to eliminate pain and restore motion.
Blood flow restricted (BFR) exercise is the brief and non-continuous blockage of venous blood flow using a device that restricts the flow of blood while exercising.
This technique is used to produce hypertrophy (muscle growth) and strength responses while exercising at a lighter load than traditionally required to produce a similar response.
Sham MFR.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Scapular retraction strength
Time Frame: 8 weeks
|
Assess scapular retraction strength with a dynamometer
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
One repetition maximum (1RM)
Time Frame: 8 weeks
|
maximum amount of weight that can be lifted one time for scapular retractors on a row machine
|
8 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Length for the pectoralis minor
Time Frame: 8 weeks
|
Assess length of the pectoralis minor with a tape measure
|
8 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)
October 16, 2023
Primary Completion (Estimated)
September 1, 2024
Study Completion (Estimated)
September 1, 2024
Study Registration Dates
First Submitted
January 12, 2023
First Submitted That Met QC Criteria
January 24, 2023
First Posted (Actual)
February 2, 2023
Study Record Updates
Last Update Posted (Actual)
March 20, 2024
Last Update Submitted That Met QC Criteria
March 19, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 22-08926-XP
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
Yes
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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