- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05606744
Effects of Blood Flow Restriction During Eccentric Resistance Exercise
November 3, 2022 updated by: Brennan Thompson, Utah State University
Effects of Blood Flow Restriction During Multiple-joint Eccentric Resistance Training on Muscle Morphology and Function of the Lower Body
The purpose of this study is to compare the muscle strength and muscle soreness effects experienced following short term (acute) eccentric exercise with and without blood flow restriction (BFR) performed at low - moderate training intensities.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
45
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: Brennan J Thompson, PhD
- Phone Number: 435-797-5785
- Email: brennan.thompson@usu.edu
Study Contact Backup
- Name: Sara Harper, PhD
- Phone Number: 435-797-1376
- Email: sara.harper@usu.edu
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
16 years to 28 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Exclusion Criteria:
- lower body surgery or injury in the last 12 months
- have any neuromuscular disease
- height >76 inches tall
- height <54 inches tall
- eccentric strength greater than 725 pounds
- pregnant or plan to be pregnant in the duration of the protocol
- don't do resistance exercise at least once per week
- perform intense cardio or strength training >4 days per week
- Present with any other significant comorbid conditions that would impair the ability to participate in the exercise-based testing
Inclusion criteria:
- 18 - 30 years old
- strength train lower body 1-3 times per week
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Eccentric exercise
Only multi-joint eccentric exercise
|
Individuals will be randomized to receive eccentric exercise only, or eccentric exercise with blood flow restriction.
|
Experimental: Eccentric training with blood flow restriction
Multi-joint eccentric exercise with blood flow restriction
|
Individuals will be randomized to receive eccentric exercise only, or eccentric exercise with blood flow restriction.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
visual analog scale (soreness)
Time Frame: Baseline (pretest)
|
soreness
|
Baseline (pretest)
|
visual analog scale (soreness)
Time Frame: immediately post exercise
|
soreness
|
immediately post exercise
|
visual analog scale (soreness)
Time Frame: 24 hours post exercise
|
soreness
|
24 hours post exercise
|
visual analog scale (soreness)
Time Frame: 48 hours post exercise
|
soreness
|
48 hours post exercise
|
visual analog scale (soreness)
Time Frame: 72 hours post exercise
|
soreness
|
72 hours post exercise
|
force algometer (soreness)
Time Frame: Baseline (pretest)
|
soreness
|
Baseline (pretest)
|
force algometer (soreness)
Time Frame: immediately post exercise
|
soreness
|
immediately post exercise
|
force algometer (soreness)
Time Frame: 24 hours post exercise
|
soreness
|
24 hours post exercise
|
force algometer (soreness)
Time Frame: 48 hours post exercise
|
soreness
|
48 hours post exercise
|
force algometer (soreness)
Time Frame: 72 hours post exercise
|
soreness
|
72 hours post exercise
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Eccentric muscle strength
Time Frame: Baseline (pretest)
|
muscle strength will be assessed on the Eccentron.
|
Baseline (pretest)
|
Eccentric muscle strength
Time Frame: immediately post exercise
|
muscle strength will be assessed on the Eccentron.
|
immediately post exercise
|
Eccentric muscle strength
Time Frame: 24 hours post exercise
|
muscle strength will be assessed on the Eccentron.
|
24 hours post exercise
|
Eccentric muscle strength
Time Frame: 48 hours post exercise
|
muscle strength will be assessed on the Eccentron.
|
48 hours post exercise
|
Eccentric muscle strength
Time Frame: 72 hours post exercise
|
muscle strength will be assessed on the Eccentron.
|
72 hours post exercise
|
Single-leg hop
Time Frame: Baseline (pretest)
|
3 single-leg hops per limb
|
Baseline (pretest)
|
Single-leg hop
Time Frame: immediately post exercise
|
3 single-leg hops per limb
|
immediately post exercise
|
Single-leg hop
Time Frame: 24 hours post exercise
|
3 single-leg hops per limb
|
24 hours post exercise
|
Single-leg hop
Time Frame: 48 hours post exercise
|
3 single-leg hops per limb
|
48 hours post exercise
|
Single-leg hop
Time Frame: 72 hours post exercise
|
3 single-leg hops per limb
|
72 hours post exercise
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Brennan Thompson, PhD, Utah State University
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 (Anticipated)
June 1, 2023
Primary Completion (Anticipated)
December 1, 2023
Study Completion (Anticipated)
March 1, 2024
Study Registration Dates
First Submitted
October 13, 2022
First Submitted That Met QC Criteria
November 3, 2022
First Posted (Actual)
November 7, 2022
Study Record Updates
Last Update Posted (Actual)
November 7, 2022
Last Update Submitted That Met QC Criteria
November 3, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 12042a
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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