The UNCODE Study: Unravelling the Neural Contributors Of Dynapenia in Elders

The UNCODE Study seeks to better identify the neurological causes of muscle weakness
associated with advancing age. The main study consists of 4 laboratory-based testing sessions
that involve testing muscle strength and physical and cognitive function as well as a battery
of tests to 1) quantify brain excitability (using single and paired pulse transcranial
magnetic stimulation of the upper and lower extremity muscles), 2) modulate brain
excitability of the upper extremity muscles (using non-invasive transcranial direct current
stimulation), 3) spinal motor nerve firing characteristics using decomposition surface
electromyography, and 4) brain structure and function characteristics based on magnetic
resonance images of the brain. Additionally, three optional sub-studies are also available
for enrollment. The first is a genetics sub-study where a cheek swab will be used to examine
associations between certain genes (APOE-4 allele) and the physiological and functional
measures obtained from the main study. The other two sub-studies are interventions. The first
sub-study is a progressive resistance exercise training study where study participants will
undergo 12-weeks of exercise training (3x/wk) and at the completion of the exercise training
the measures obtained in the main study will be re-assessed. The other sub-study is a mental
imagery sub-study where subjects are randomly assigned to perform a mental imagery training
program consisting of imaging strong muscle contractions and mobility tasks (5x/wk) or to
serve as a control (i.e., to not modify lifestyle) for 6-weeks. At the completion of the
respective intervention period the measures obtained in the main study will be re-assessed.

Inclusion Criteria:

- Age 60+ years with no significant health issues or conditions that, in the
investigator's opinion, would limit the subject's ability to complete the study per
protocol or that would impact the capability to get an accurate measurement of study
endpoints.

- Body mass index between 16.0 and 40.0 kg/m2.

- With no condition that would limit participation in supervised resistance training
exercise based on the Physical Activity Readiness Questionnaire (PAR-Q) (for the
"Resistance Exercise Training Sub-Study only).

- Willingness to maintain current diet and adhere to the intervention programs described
for the sub-studies (if applicable) and willing to undergo all testing procedures.

- Able to read, understand, and complete study-related questionnaires

- Able to read and understand, and willing to sign the informed consent form (ICF).

Exclusion Criteria:

- Failure to provide informed consent.

- Any activity of daily living (ADL) disability (difficulty feeding, dressing,
continence, bathing, toileting, and transferring).

- Lives in a nursing home; persons living in assisted or independent housing will not be
excluded.

- Cognitive impairment, defined as a known diagnosis of dementia or Modified Mini-Mental
State exam score <24

- Known neuromuscular or neurological conditions affecting somatosensory or motor
function or control (e.g., hemiplegia, multiple sclerosis, peripheral neuropathy,
Parkinson's disease, Myasthenia Gravis, Ataxia, Apraxia, post-polio syndrome,
mitochondrial myopathy, etc.).

- Unable to communicate because of severe hearing loss or speech disorder.

- Severe visual impairment, which would preclude completion of the assessments.

- Cancer requiring treatment currently or in the past 2 years (except primary
non-melanoma skin cancer or in situ cervical cancer)

- Hospitalization (medical confinement for ≥24 hours), or immobilization, or major
surgical procedure requiring general anesthesia within 12 weeks prior to screening, or
any planned surgical procedures during the study period.

- Chronic or relapsing/remitting gastrointestinal disorders such as inflammatory bowel
disease and irritable bowel syndrome.

- Known history of human immunodeficiency virus (HIV) antibody at screening.

- Use of systemic glucocorticoids.

- Severe pulmonary disease, requiring either steroid pills or injections or the use of
supplemental oxygen.

- Severe cardiac disease, including New York Heart Association (NYHA) Class III or IV
congestive heart failure, clinically significant aortic stenosis, recent history of
cardiac arrest (within 6-months), use of a cardiac defibrillator, or uncontrolled
angina.

- Renal failure on hemodialysis

- Psychiatric conditions that warrant acute or chronic therapeutic intervention (e.g.,
major depressive disorder, bipolar disorder, panic disorder, schizophrenia) that in
the investigators opinion may interfere with the conduct of study procedures

- Unable to undergo MRI or transcranial magnetic stimulation (TMS) (e. g. body
containing any metallic medical devices or equipment, including heart pacemakers,
metal prostheses, implants or surgical clips, any prior injury from shrapnel or
grinding metal, exposure to metallic dusts, metallic shavings or having tattoos
containing metallic dyes).

- Unable to reliably undergo exercise or strength tests described for this study.

- Participation in progressive resistance exercise within the previous 24 weeks prior to
screening (for sub-studies only).

- Participation in any clinical trial within 12 weeks prior to screening (for
sub-studies only).

- Limb amputation (except for toes) and/or any fracture within 24 weeks.

- Osteoarthritis, rheumatologic diseases or orthopedic disorders that will not allow
completion of the motions required for the resistance exercise (for Resistance
Exercise Training Sub-Study only).

- Conditions (such as myasthenia gravis, myositis, muscular dystrophy or myopathy,
including drug-induced myopathy) leading to muscle loss, muscle weakness, muscle
cramps or myalgia.

- Acute viral or bacterial upper or lower respiratory infection at screening

- Abnormal or uncontrolled blood pressure at the screening visit defined as diastolic BP
>100 and/or systolic BP >170 mm Hg; if taking anti-hypertensive medication, have to be
on stable doses of medication for more than 3 months.

- Medications known to alter the investigators' primary TMS-based outcomes. For
instance, individuals taking benzodiazepines will be excluded from study
participation.

- Current or recent history (within 1 year of screen) of heavy alcohol consumption or
drug abuse that in the investigators opinion may interfere with the conduct of study
procedures.

- Subjects with the following abnormal ECG findings at screening will be excluded:
Electrocardiogram findings indicative of left ventricular hypertrophy (LVH) (based on
Cornell voltage criteria):

- For men: S in V3 plus R in a VL >2.8 milliVolts (mV) (28 mm)

- For women: S in V3 plus R in a VL >2.0 mV (20 mm)

- Electrocardiogram finding of QT prolongation