A Comparison of Neuromuscular Recruitment in Trained and Untrained Adults

Inclusion Criteria

• Participant must have a BMI between 18.5 and 38

• Participant be aged between 60 and 85

• Regularly exercises at least 5 days a week a minimum of 30 minutes per day.

• Engages in less than 2 days of exercise less than 30 minutes each day.

• Participant must use the Mayo Clinic patient online portal.

• Participant must be able to understand English without the need of an interpreter.

• Must be willing to be contacted for research

• Participant must be willing and capable to provide consent.

• Participants shall be generally healthy as deemed acceptable by the principalinvestigator

• Men and women will be participant in this study. Women cannot be pregnant duringthis study.

Exclusion Criteria:

• Surgical History - Gastric surgery, pacemaker placement, weight loss surgery,metabolic and obstetric surgery.

• Smokers will be excluded from the study.

• Medications: Insulins, common diabetic drugs, anti-hyperglycemic drugs, betablockers cardiac selective, beta-blockers noncardiac selective, oral steroids,opioids anti-depressants, and hormones

• Conidiations and Diagnosis: Disorder of coronary artery, hepatic failure,gastroparesis, disorder of the adrenal gland, drug related disorders, substanceabuse, malignant neoplastic disease, psychotic disorders, disorder of skeletalmuscle, finding of brain, chronic kidney disease, renal failure syndrome, disorderof pulmonary circulation, cerebrovascular disease, neuro developmental disorder,disorder of immune function, disorder of central nervous system.

• Participants are not to have an abnormal value as part of a lipid panel within thepast 6 months.

• Participant will be excluded if they have recreational drug use or a history ofalcohol abuse

• Inability or unwillingness of individual or legal guardian/representative to givewritten informed consent.

• Current or past participation within a specified timeframe in another clinicaltrial, as warranted by the administration of this intervention.

• Participant will be excluded if they have epilepsy.

• Participant will be excluded if they have cranial metal/device implants

• Participant will be excluded if they are pregnant