Resistance Training Clinical Trial
Official title:
Influence of Resistance Training Experience on the Efficacy of Mental Imagery in Modulating Corticospinal Excitability and Inhibition: A Pilot Study
Verified date | February 2023 |
Source | University of Central Florida |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will utilize transcranial magnetic stimulation (TMS) to examine the effects of mental imagery in resistance-trained versus untrained men and women. In randomized order, each participant will perform a mental imagery task or a control condition as TMS is used to study corticospinal excitability.
Status | Completed |
Enrollment | 60 |
Est. completion date | January 1, 2023 |
Est. primary completion date | January 1, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 35 Years |
Eligibility | Inclusion Criteria: - Over the previous six months, participant has performed at least three resistance training sessions per week or - Over the previous six months, participant has refrained from resistance training entirely. Exclusion Criteria: - Do not meet the resistance training experience requirements of either group - Neuromuscular disease (e.g. Parkinson's, MS, ALS) - Metabolic disease (e.g. diabetes, thyroid disorder, metabolic syndrome) - Arthritis in the upper limbs (hands, arms, shoulders) - Trouble using or controlling one's muscles - History of cancer - History of stroke - History of heart attack - Use of an assistive walking device or other mobility aids - Physician mandated contraindication to exercise within the last 6 months - Epilepsy or history of convulsions/seizures - History of fainting or syncope - History of head trauma that was diagnosed as concussion or was associated with loss of consciousness - History of hearing problems or tinnitus - Cochlear implants - Implanted metal in the brain, skull, or elsewhere in the body - Implanted neurotransmitter - Cardiac pacemaker or intracardiac lines - Medication infusion device - Past problems with brain stimulation - Past problems with MRI - Use of muscle relaxants or benzodiazepines - Allergy to rubbing alcohol - Any other health related illnesses that would prohibit a participant from physical performance testing - Lack of transportation to and from the laboratory - Any permanent / non-removable jewelry or metal fixtures |
Country | Name | City | State |
---|---|---|---|
United States | Central Florida Research Park; Partnership 1 Building; UCF Neuromuscular Plasticity Laboratory | Orlando | Florida |
Lead Sponsor | Collaborator |
---|---|
University of Central Florida |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Corticospinal Excitability | Peak-to-peak amplitude of the motor evoked potential of the first dorsal interosseous at 130% of resting motor threshold | Greater than or equal to 24 hours to 7 days between visits. |
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