Eccentric Resistance Training With Blood Flow Restriction on Muscle Function

Sponsor
Sara Harper (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04977804
Collaborator
(none)
30
2
6

Study Details

Study Description

Brief Summary

The study will determine the effects of adding blood flow restriction to eccentric training to assess whether this increases the improvements of muscle strength and size.

Condition or Disease Intervention/Treatment Phase
  • Other: Exercise
  • Other: Eccentric plus blood-flow restriction
N/A

Detailed Description

Subjects will be randomly assigned to two groups: an eccentric only resistance training group or an eccentric training plus blood flow restriction group. Subjects will train at a moderately low intensity on a multiple-joint eccentric device. Those in the blood flow restriction will wear blood flow restriction cuffs on their upper thighs to reduce blood flow during the brief protocol. The training session will occur twice per week and will last ~5 minutes, including a one minute warm up, a one minute cool down and a three minute workout phase. The training program will last 7 weeks. Testing will be conducted at baseline (following a one session familiarization), 4 weeks and after the end of the 7 week training period. Assessments will focus on muscle strength, function, and morphology (size).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two group, randomized parallel group design.Two group, randomized parallel group design.
Masking:
Single (Outcomes Assessor)
Masking Description:
The person assessing the outcome measures will be blinded to the group designation of the subjects.
Primary Purpose:
Basic Science
Official Title:
Effects of Blood Flow Restriction During Multiple-joint Eccentric Resistance Training on Muscle Morphology and Function of the Lower Body.
Anticipated Study Start Date :
Sep 30, 2022
Anticipated Primary Completion Date :
Apr 1, 2023
Anticipated Study Completion Date :
Apr 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Eccentric only training

This is the experimental control; where this group will be used as the standard active comparison condition.

Other: Exercise
The interventions are a form or exercise, specifically resistance exercise.

Experimental: Eccentric plus blood-flow restriction

This is the experimental condition involving the eccentric resistance training with blood flow restriction.

Other: Eccentric plus blood-flow restriction
Eccentric plus blood-flow restriction

Outcome Measures

Primary Outcome Measures

  1. Eccentron maximal muscle strength [7 weeks]

    Eccentric muscle strength will be assessed via Eccentron (BTE Technologies, Inc., USA), an seated isokinetic dynamometer.

  2. Local muscle hypertrophy [7 weeks]

    Muscle size changes of the quadriceps muscle measured an ultrasound device (GE NextGen LOGIQ, Tampa, Florida, USA).

  3. Muscle mass [7 weeks]

    dual energy x-ray absorptiometry device (DEXA) the Hologic Horizon W Dual X-ray absorptiometry (Hologic Canada ULC, Mississauga, ON, Canada) will be used to assess appendicular (lower body) mean mass.

  4. Muscle function [7 weeks]

    Vertical jump height will assess 3 maximal countermovement attempts on a jump mat (Just Jump Technologies, Huntsville, AL, USA) that measures jump height based on flight time.

Secondary Outcome Measures

  1. Muscle soreness [7 weeks]

    local muscle soreness will be assessed throughout the duration of the intervention period using a Wagner force algometer.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 30 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 18-30 years of age

  • currently engaged in some form of resistance training between 1-3 times per week

  • must have been training aerobically, but no more than 3 hours a week for the past six months

Exclusion Criteria:
  • Must not have had any surgery of the lower limbs within the past 1 year period

  • Must not have any neuromuscular disorder (e.g., Muscular dystrophy etc.)

  • < 76 inches tall (in order to fit on the training machine)

  • Maximal strength of < 725 lbs for the eccentric training device

  • If any of the subjects are pregnant or plan to be pregnant in the duration of the protocol.

For those randomized to the BFR group, if any of the subject's thighs are too large for the BFR cuffs (greater than 68 cm).

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Sara Harper

Investigators

  • Principal Investigator: Brennan J Thompson, PhD, Utah State Univeristy

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sara Harper, Co-Principal Investigator, Utah State University
ClinicalTrials.gov Identifier:
NCT04977804
Other Study ID Numbers:
  • 12042
First Posted:
Jul 27, 2021
Last Update Posted:
May 17, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sara Harper, Co-Principal Investigator, Utah State University

Study Results

No Results Posted as of May 17, 2022