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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02987491
Other study ID # 7605
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 2016
Est. completion date June 28, 2018

Study information

Verified date August 2019
Source Oregon State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Obesity is associated with a decrease in skeletal muscle insulin sensitivity. Aerobic exercise can increase insulin sensitivity in the few hours following exercise, however the cellular mechanisms are not completely understood. The current project is to investigate mechanisms of exercise improvements to skeletal muscle insulin sensitivity.


Description:

Study Overview: We are investigating the mechanisms by which exercise improves the response of skeletal muscle to insulin in lean and obese adults. Participants will complete 4 study visits consisting of: 1) screening visit, 2) maximal exercise test visit, and then a randomized order of 3) a resting metabolic study visit, and 4) an exercise metabolic study visit. Metabolic study visits for resting and exercise conditions will be identical, other than remaining sedentary or performing exercise. Skeletal muscle biopsy samples will be collected during resting, immediately post-exercise and during insulin stimulated conditions.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 28, 2018
Est. primary completion date June 28, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Males or Females

- Aged 18-45 years

- Normal weight (body mass index [BMI] 18-26 kg/m2) or obese (BMI 30-46 kg/m2)

- Sedentary (< 1 hour of planned physical activity per week for = 6 months)

- Weight stable (< 2 kg change in body mass for = 6 months)

- Non-smokers (no tobacco or nicotine use for = 1 year)

Exclusion Criteria:

- Hypertension (systolic blood pressure >140 mmHg, diastolic blood pressure > 90mmHg)

- Chronic health condition including diabetes, cardiovascular disease, treated hypertension, cancer, anemia, uncontrolled hyper- or hypothyroidism.

- Pregnant, nursing, irregular menses or post-menopausal (if female)

- Hyperglycemia (fasting glucose >126 mg/dl)

- Hypercholesterolemia (fasting LDL>140mg/dl)

- Hemoglobin < 13.0 g/dl (males), < 11.5 g/dl (females)

- Compromised renal function (outside 135-145 mmol/L sodium, 3.5-5.1 mmol/L potassium)

- Lidocaine allergy

- Medications including ß-blockers, angiotensin converting enzyme inhibitors, insulin, thiazolidinediones, metformin, sulfonylureas, chronic non-steroidal anti-inflammatory use, anti-coagulant (e.g. warfarin), current antibiotics, opiates, monoamine oxidase inhibitors, benzodiazepines, or others that may impact the study outcomes

- Any physical limitation that prevents a participant from safely completing the exercise test

- Due to the risks associated with the current protocol, individuals with a diminished capacity to consent will be excluded. Similarly, due to the need for constant, accurate participant monitoring during metabolic study activities, participants will need to clearly understand verbal and written English. Participants who cannot clearly understand verbal and written English will be excluded.

Study Design


Intervention

Behavioral:
Exercise
Participants will perform 2 metabolic study days of either resting or acute bout of cycling exercise in a randomized cross-over design.

Locations

Country Name City State
United States Oregon State University Corvallis Oregon

Sponsors (1)

Lead Sponsor Collaborator
Oregon State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Skeletal muscle insulin sensitivity Skeletal muscle insulin sensitivity will be measured by hyperinsulinemic-euglycemic clamp. 2 hours following rest or exercise
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