- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05084690
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
Status
Enrolling by invitation
Conditions
Intervention / Treatment
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.
Sponsor
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021-102
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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