Mirror Illusion Training and Cross-education

October 7, 2021 updated by: Joshua Carr, Texas Christian University

Mirror Illusion Training to Improve Contralateral Arm Strength

Cross-education describes the transfer of motor performance to the opposite limb following unilateral training and is primarily explained by adaptations within the brain. The mirror training hypothesis suggests that illusionary mirror visual feedback may augment the cross-education of strength to the untrained, contralateral limb. The purpose of this project is to examine how the use of illusionary mirror visual feedback shapes the neuromuscular adaptations that occur for both limbs during unilateral (single-limb) strength training. Our hypothesis is that mirror training will augment the level of cross-education for the untrained arm.

Study Overview

Detailed Description

Recent empirical evidence shows a heightened level of strength transfer with the use of illusionary mirror visual feedback, but this was shown for the small muscles of the wrist during isokinetic training. It is unknown if larger, multi-joint muscles respond favorably to mirror training in practical settings. A randomized controlled study design will allocate approximately 20 participants into two groups. One group will perform unilateral strength training with illusionary mirror visual feedback (Mirror) and the other will perform the same unilateral strength training but without a mirror (No-Mirror). The intervention will involve four weeks of unilateral strength training performed twice weekly at high intensities (>80%1RM).

Study Type

Interventional

Enrollment (Anticipated)

20

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

    • Texas
      • Fort Worth, Texas, United States, 76126
        • TCU Neuromuscular Physiology Laboratory
      • Fort Worth, Texas, United States, 76126
        • TCU RIC

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 35 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • right-hand dominance
  • no previous strength training of upper body last 3 months
  • no injuries or recent surgeries of the upper limbs
  • willingness to adhere to the strength training requirements of the study

Exclusion Criteria:

  • current use of hormone replacement therapy
  • pregnancy/breastfeeding

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Resistance training control group
The resistance training control group will perform unilateral resistance training on their dominant arm. The training will be performed twice per week for four weeks totaling eight training sessions.
Unilateral resistance training of the elbow flexors
Experimental: Resistance training with mirror illusion group
The resistance training with mirror illusion group will perform unilateral resistance training on their dominant arm. During training, they will view a mirror illusion of their exercising arm over their opposite, non-exercising arm. The training will be performed twice per week for four weeks totaling eight training sessions.
Unilateral resistance training of the elbow flexors
Modified Ramachandran's mirror box

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in dynamic muscle strength for the trained and untrained arm
Time Frame: Baseline (week 0) post-training (week 5)
Dynamic 1-repetition maximum (lbs)
Baseline (week 0) post-training (week 5)
Change in isometric muscle strength for the trained and untrained arm
Time Frame: Baseline (week 0) post-training (week 5)
Isometric maximal voluntary contraction
Baseline (week 0) post-training (week 5)
Change in lean mass for the trained and untrained arm
Time Frame: Baseline (week 0), mid-training (week 2), post-training (week 5)
DEXA (g)
Baseline (week 0), mid-training (week 2), post-training (week 5)
Change in muscle thickness for the trained and untrained arm
Time Frame: Baseline (week 0), mid-training (week 2), post-training (week 5)
Ultrasound muscle thickness (cm)
Baseline (week 0), mid-training (week 2), post-training (week 5)
Change in muscle activation for the trained and untrained arm
Time Frame: Baseline (week 0) post-training (week 5)
Electromyographic amplitude (volts)
Baseline (week 0) post-training (week 5)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Joshua C Carr, Texas Christian 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 (Actual)

July 19, 2021

Primary Completion (Anticipated)

August 19, 2023

Study Completion (Anticipated)

August 19, 2023

Study Registration Dates

First Submitted

October 7, 2021

First Submitted That Met QC Criteria

October 7, 2021

First Posted (Actual)

October 20, 2021

Study Record Updates

Last Update Posted (Actual)

October 20, 2021

Last Update Submitted That Met QC Criteria

October 7, 2021

Last Verified

October 1, 2021

More Information

Terms related to this study

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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