- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06627491
Influence of Fast and Slow Imagined Muscle Contractions on Muscle Function or Central Nervous System Properties
Does the Speed of Imagined Muscle Contractions Affect Muscle Function and Central Nervous System Excitability?
The goal of this randomized clinical trial is to learn if imagining fast or slow muscle contractions causes different responses for nervous system excitability and muscle function in young, healthy males and females in. The main questions are:
Does imagining fast muscle contractions cause greater nervous system excitability compared to imagining slow muscle contractions?
Does imagining fast muscle contractions increase muscle function compared to imagining slow muscle contractions?
A control condition (rest) will be compared with two intervention conditions: imagining fast and imagining slow conditions, to determine if the fast and slow increase outcomes more than control and if fast has the greatest response.
Participants will:
- Attend 4 laboratory visits
- Perform 50 imagined contractions fast or slow, but with no physical movement
- Physical muscle contractions and non-invasive brain stimulation would be completed before and after each condition.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Garrett Hester, Ph.D.
- Phone Number: 470-578-4267
- Email: ghester4@kennesaw.edu
Study Locations
-
-
Georgia
-
Kennesaw, Georgia, United States, 30144
- Recruiting
- Kennesaw State University
-
Contact:
- Garrett Hester, Ph.D.
- Phone Number: 470-578-4267
- Email: ghester4@kennesaw.edu
-
Contact:
- Garrett Hester, Ph.D.
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Be between the ages of 18 - 30
- Healthy (no medical conditions)
- If female, must be taking the same monophasic oral contraceptive for the past 6 months
- Have a body mass index between 18.5 - 30 kg/m2
- Have not performed structured cardiovascular or resistance exercise in past 3 years
- Be right-handed
- Not currently taking stimulants, antipsychotic, anxiety, or depression medications
- Have not suffered an upper extremity musculoskeletal injury within the past year
Exclusion Criteria:
- If transcranial magnetic stimulation (TMS) is not deemed appropriate depending on your responses to the TMS-specific questionnaire
- Being ambidextrous
- Although rare, you will be excluded if discernable muscle activation responses are not possible via TMS
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
Participants will rest quietly with eyes closed during the control condition.
|
|
|
Experimental: Fast
Participants will imagine 2 blocks of 25 fast muscle contractions separated by 30 sec
|
The intervention involved imagining, with no physical movement, of muscle contractions.
|
|
Experimental: Slow
Participants will imagine 2 blocks of 25 slow muscle contractions separated by 30 sec
|
The intervention involved imagining, with no physical movement, of muscle contractions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in rate of torque development as measured by newton-meters per second
Time Frame: Baseline, minute 20
|
A measure of the capacity to increase muscle torque rapidly as determined by the slope of the torque-time curve
|
Baseline, minute 20
|
|
Change in nervous system excitability as measured by electromyographic waveform aplitude following motor cortex stimulation
Time Frame: Baseline, minute 20
|
A measure of excitability for the corticospinal tract
|
Baseline, minute 20
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in isometric bicep strength as measured by newton-meters of torque
Time Frame: Baseline, minute 20
|
Isometric strength of a muscle
|
Baseline, minute 20
|
|
Change in agonist muscle activation as measured by electromyography amplitude
Time Frame: Baseline, minute 20
|
A measure of the capacity at which the muscle is activated by the nervous system
|
Baseline, minute 20
|
|
Change in antagonist co-activation as measured by electromyography amplitude
Time Frame: Baseline, minute 20
|
A measure of the capacity at which the antagonist muscle is activated by the nervous system
|
Baseline, minute 20
|
|
Change in rate of agonist muscle activation as measured by electromyography amplitude
Time Frame: Baseline, minute 20
|
A measure of how quickly the nervous system activates the muscle
|
Baseline, minute 20
|
|
Change in nervous system inhibition as measured by electromyographic waveform aplitude following motor cortex stimulation
Time Frame: Baseline, minute 20
|
A measure of inhibition for the corticospinal tract
|
Baseline, minute 20
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-reported ability to imagine movements as measured by Movement Imagery Questionnaire-Revised as measured on a scale from 8 to 56
Time Frame: Baseline
|
Survey that estimates one's capacity to imagine movement.
A higher score indicates better imagination.
|
Baseline
|
|
Level of vividness for imagining the imagined contractions as measured by 7-point likert scale as measured from 1 to 7
Time Frame: 20 minutes after baseline
|
A 7-point likert scale is used to to determine how vivid one's imagination was for the conditions.
A higher score indicates greater difficulty imagining the movement.
|
20 minutes after baseline
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- MI_KA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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