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

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

Study Contact Backup

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.

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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