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NCT04158375Completed

Molecular Mechanisms of Exercise Benefits to Insulin Resistant People

Source: ClinicalTrials.gov · Last updated 25 Nov 2025

Brief summary (registry, in English)

This proposal will investigate the underlying mechanisms of enhanced insulin sensitivity and improvement of muscle loss and performance in insulin resistant people by resistance exercise training. Based on the investigator's preliminary data, they hypothesize that the key regulators of health benefits of resistance training are two genes: PGC-1a4 and PPARB;, and that the increased expression of these genes following resistance training facilitates storage of glucose in muscle and enhances its utilization for the energy need of muscle for contraction as well as enhancing muscle mass and performance. The investigators will also determine whether resistance training can reduce the higher oxidative stress in insulin resistant humans and improve their muscle protein quality.

Status (registry)
Completed
Study type
Interventional
Enrollment
58 (actual)
First submitted
5 Nov 2019
Start date
2 Sept 2020
Primary completion date
17 Sept 2024
Lead sponsor
Mayo Clinic
Diseases
Obesity
NCT number
NCT04158375

What you commit to

  • Study type: Interventional
  • Participants enrolled: 58
  • From 2 Sept 2020 to the primary completion date, 17 Sept 2024
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Coronary artery disease or heart failure.

Lab values

  • A known medical condition that in the judgment of the investigator might interfere with the completion of the protocol such as the following examples:
    • Inpatient psychiatric treatment in the past 6 months
    • Presence of a known adrenal disorder
    • Abnormal liver function test results (Transaminase \>2 times the upper limit of normal); testing required for subjects taking medications known to affect liver function or with diseases known to affect liver function
    • Abnormal renal function test results (calculated GFR \<60 mL/min/1.73m2); testing required for subjects with diabetes duration of greater than 5 years post onset of puberty
    • Active gastroparesis
    • If on antihypertensive, thyroid, anti-depressant or lipid lowering medication, lack of stability on the medication for the past 2 months prior to enrollment in the study
    • Uncontrolled thyroid disease (TSH undetectable or \>10 mlU/L); testing required within three months prior to admission for subjects with a goiter, positive antibodies, or who are on thyroid hormone replacement, and within one year otherwise
    • Abuse of alcohol or recreational drugs
    • Infectious process not anticipated to resolve prior to study procedures (e.g. meningitis, pneumonia, osteomyelitis).
    • Uncontrolled arterial hypertension (Resting diastolic blood pressure \>90 mmHg and/or systolic blood pressure \>160 mmHg) at the time of screening.
    • Oral steroids
    • A recent injury to body or limb, muscular disorder, use of any medication, any carcinogenic disease, or other significant medical disorder if that injury, medication or disease in the judgment of the investigator will affect the completion of the protocol
    • Restrictions on Use of Other Drugs or Treatments:
    • Medications that may impact study end points such as mitochondrial biology eg. beta blockers
    • Anti-hyperglycemic drugs including metformin
    • Any other medication that the investigator believes is a contraindication to the subject's participation.

Other

  • Participation in a structured exercise program \>2 days per week

Who the study is looking for

  • age 50-75yrs
  • BMI 30-38kg/m2
  • hip to waist ratio of \>0.85 in women and 1.0 in men
  • fasting glucose ≥100-140mg/dl
    • Lean Group
  • age 50-75 years
  • hip to waist ratio of \<0.76 in women and 0.90 in men
  • fasting glucose of \<100mg/dl.

Age in the registry: 50 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Mayo Clinic in Florida
Coordinator of this site? Confirm its status
JacksonvilleUnited StatesUnknown status
Mayo Clinic in Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status
Mayo Clinic in Arizona
Coordinator of this site? Confirm its status
ScottsdaleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.