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CompletedNCT00882986Updated Sep 24, 2015

Cardiovascular and Metabolic Responses to a Mixed Meal

An observational study in Insulin Resistance, sponsored by John Thyfault. Completed at 1 site in United States. Open to male participants aged 20 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-09-24.

Sponsored by John Thyfault · Observational

Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
20
Ages
20 Years to 50 Years
Sex
Male
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Study summary

The purpose is to determine whether regular endurance exercise and/or body weight influence the way our nervous and vascular systems respond during the metabolism of meals.

Read the detailed description

To begin to examine this question we recruited healthy endurance-trained (high fit, HF) and normally active (average fit, AF) subjects. It is well characterized that chronic endurance training results in enhanced peripheral insulin sensitivity. Therefore, our rationale was that inclusion of two healthy subject groups, with distinct differences in insulin sensitivity, would allow us to investigate how enhanced insulin sensitivity influences insulin-mediated changes in central sympathetic outflow. Direct measurements of central sympathetic outflow to skeletal muscle (i.e., MSNA) were recorded, and a mixed meal was used as a physiological method to evoke robust and sustained increases in MSNA, which have been primarily attributed to insulin. We hypothesized that HF subjects would have a greater MSNA response, for a given plasma insulin concentration, following consumption of a mixed meal (i.e., greater central insulin sensitivity).

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Conditions studied

  • Insulin Resistance

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Keywords

  • insulin resistance
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In context

Insulin Resistance

1,960 studies on the registry are indexed under Insulin Resistance; 306 are open to participants now.

This study's enrollment of 20 is below the median of 80 across 339 observational studies indexed under Insulin Resistance.

Browse Insulin Resistance studies →

Lead sponsor

This is the only study on the registry with John Thyfault as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 50 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

young, lean, healthy men

Inclusion criteria

  • healthy, not currently taking any medications

Exclusion criteria

Exclusion Criteria:

  • unhealthy, taking medications
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Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
20 participants (actual)
Patient registry
No

Groups and cohorts

  • 1

    Men with high fitness (above VO2max of 60)

  • 2

    Men with average fitness (below VO2max of 50)

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What researchers measure

Primary outcomes

  1. insulin/glucose response to mixed meal ingestion

    Time frame: This study is cross-sectional. Primary and secondary measures will be assessed at a single timepoint.

Secondary outcomes

  1. MSNA

    Time frame: This is a cross-sectional study. Primary and seconardy measures will be assessed at a single visit lasting 4-6 hours.

  2. Blood flow

    Time frame: This is a cross-sectional study. Primary and seconardy measures will be assessed at a single visit lasting 4-6 hours.

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Study locations

1 site
  • University of Kansas Medical Center
    Kansas City, Kansas 66160, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 24, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00882986
Lead sponsor
John Thyfault
Responsible party
John Thyfault (Associate Professor, University of Kansas Medical Center) — Sponsor-investigator
First posted
Apr 17, 2009
Start date
Jan 2009
Primary completion
Aug 2011
Completion
Aug 2011
Last update
Sep 24, 2015

Study contacts

John P Thyfault, PhD
principal investigator · University of Kansas Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2015. You cannot join it, but the record below documents what was studied.

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