Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03889548
Other study ID # 00000170
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 7, 2019
Est. completion date January 1, 2023

Study information

Verified date February 2023
Source University of Central Florida
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Kinesthetic mental imagery is a technique that has previously been utilized to modulate neural signaling to the limbs in the absence of any mechanical movement of the limb. Kinesthetic imagery tasks require an individual to imagine they are maximally contracting a target muscle group. Previous investigations have shown mental imagery tasks to increase maximal strength of the limb and even attenuate strength loss during periods of immobilization. Similarly, corticospinal excitability, which indicates the ease in which the cortex can stimulate muscular contraction, has also been shown to increase during mental imagery tasks. These adaptations have been attributed to the role of the cortex as a critical determinant of strength and the potent cortical stimulus posed by mental imagery. Mental imagery and resistance training have both shown to provide a positive impact on muscle strength. However, the interplay between a mental imagery task and resistance training experience has yet to be fully investigated in terms of their impact on corticospinal excitability and inhibition. To our knowledge, no study has examined the effect of resistance training experience on corticospinal excitability and inhibition during a mental imagery task. Thus, the purpose of this study is to determine if resistance trained and untrained participants experience differences in corticospinal excitability and inhibition during kinesthetic mental imagery.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mental Imagery
Immediately after determination of the resting motor threshold and pre-test measurements, the TMS administrator will leave the room so as to be blinded to the treatment condition of the participant. At this time the participant will be given instructions regarding the mental imagery protocol from a separate investigator who will not be blinded to the condition. During the mental imagery protocol, participants will be instructed to close their eyes and imagine they are maximally contracting the muscles in their forearm and imagine that they are making their wrist flex and that they are pushing maximally against a hand grip in their hand. This will be a kinesthetic imagery task, in which they are urging their muscles to contract maximally.

Locations

Country Name City State
United States Central Florida Research Park; Partnership 1 Building; UCF Neuromuscular Plasticity Laboratory Orlando Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Central Florida

Country where clinical trial is conducted

United States, 

Outcome

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.
See also
  Status Clinical Trial Phase
Completed NCT05987046 - Contrast Training, Post-activation Countermovement Jump Performance in High Strength Male N/A
Completed NCT04136821 - The Long-term Effects of Oceanix™ on Resistance Training Adaptations N/A
Recruiting NCT05945641 - Effect of Low-load Resistance Training vs. High-intensity Interval Training on Local Muscle Endurance N/A
Completed NCT04069351 - Body Composition Changes During Overfeeding Plus Resistance Training N/A
Not yet recruiting NCT06360536 - Remotely Delivered Resistance Training for Cardiometabolic Health Among Black Women N/A
Completed NCT04535596 - Blood Flow Restriction Exercises and Conservative Exercises in Knee Osteoarthritis N/A
Completed NCT04213586 - Effects of Whey Protein and Collagen Supplementation N/A
Completed NCT05052164 - Improvement Of Physical And Physiological Parameters In Menopausal Or Post-Menopausal Celiac Women N/A
Completed NCT04630951 - Blood Flow Restriction Strength Training in Professional Soccer Players N/A
Not yet recruiting NCT03722277 - Variable Resistance Training in Patients With Osteoarthrosis of the Knee N/A
Completed NCT00991523 - Overnight Post-Exercise Recovery After Protein Ingestion Prior to Sleep N/A
Completed NCT01216722 - Study of Resistance Strengthening Versus Ambulation Post-Liver Transplant N/A
Recruiting NCT06131125 - Plyometric vs Explosive Strength Training on Agility, Power, and Balance in Basketball Players N/A
Recruiting NCT06131138 - Aquatic Exercises VS Core Strengthening on Disability, Flexibility and Postural Stability in Weightlifters. N/A
Recruiting NCT06131047 - High Intensity Resistance Training With and Without Blood Flow Restriction in ACL Reconstruction N/A
Recruiting NCT06240962 - Mindfulness Practice vs Strength Training on Pain, Kinesiophobia and Function Among Sprinters N/A
Completed NCT04315077 - The Short Term Effects of Oceanix Supplementation on Recovery N/A
Completed NCT05597423 - Massage as Recovery Strategy After Resistance Training N/A
Completed NCT02327975 - Prescription of Physical Exercise Through Mobile Application in Elderly N/A
Active, not recruiting NCT06171841 - Effects of Low-Intensity Blood Flow Restriction Training in Normoxia and Hypoxia Conditions N/A