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NCT03019510 · ClinicalTrials.gov registry record · NA

Lowering Impaired Fasting Glucose Levels With Exercise

A NA study, sponsored by University of Missouri-Columbia.

Completed
Registry status
NA
Development phase
54
Enrollment target

NCT03019510: Completed NA study, sponsored by University of Missouri-Columbia.

NCT03019510 is a NA study that has completed, run by University of Missouri-Columbia. The registered enrollment target is 54 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03019510, a NA study, has completed, sponsored by University of Missouri-Columbia.

COMPLETED
Registry status
NA
Development phase
54 participants
Enrollment target

Study Summary

Morning hyperglycemia plays a role in the future development of insulin resistance and type 2 diabetes (T2D) (8) and is associated with numerous microvascular and cardiovascular complications and renal disease. These augmented morning glucose levels are due to an elevated endogenous glucose production (EGP), as a result of a loss of coordination between glucose levels and insulin secretion, and possibly hyperglucagonemia during the overnight period. Exercise stimulates glucose uptake and increases insulin sensitivity acutely, and may be the best lifestyle intervention to minimize the nocturnal rise in glucose levels. Prescription of the timing of exercise relative to a meal and/or to the overnight period may be particularly critical for individuals that have impaired fasting glucose (IFG) levels. Surprisingly little is known about the overnight period when elevated EGP and the synchrony between glucose and c-peptide/glucagon levels becomes disturbed. This novel study will provide insight into the hormonal/metabolic milieu of a dinner meal, the evening and overnight period that occurs in non-obese, OB and OB+IFG individuals; it will also establish if the timing of exercise can attenuate nocturnal glucose elevations, and if this is associated with improved hormonal synchrony. This project will compare EGP, β-cell function and hormonal responses between morning and evening exercise on the postprandial and overnight period in obese individuals with/without IFG levels. Fifty-four subjects will be studied during the evening meal (EGP and β-cell function), postprandially and through the overnight period (1600-0700 h), allowing us to examine some of the potential mechanisms for the elevation in overnight glucose levels. This is the first study that will examine this issue from pre-dinner through the night while previous studies have only examined chronically fasted individuals and this study will lay the groundwork for understanding the pathology of the predawn phenomena in

Primary Outcome

the hour prior to study completion will be used for this measurement

Interventions

  • BEHAVIORAL No exercise
  • BEHAVIORAL Morning exercise
  • BEHAVIORAL Evening exercise

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2016-10
Est. Completion 2021-09-30
Phase NA
University of Missouri-Columbia

291 total trials

What the finished NCT03019510 record still lists

NCT03019510 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 54 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 3 interventions - of which No exercise is the first listed.

NCT03019510 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03019510 about?

NCT03019510 is a clinical study titled "Lowering Impaired Fasting Glucose Levels With Exercise". Morning hyperglycemia plays a role in the future development of insulin resistance and type 2 diabetes (T2D) (8) and is associated with numerous microvascular and cardiovascular complications and renal disease. These augmented morning glucose levels are due to an elevated endogenous glucose producti...

What is the current status of trial NCT03019510?

This trial is currently completed. It is a NA study. The enrollment target is 54 participants. The study started on 2016-10. Estimated completion is 2021-09-30.

What interventions are being tested in trial NCT03019510?

The interventions under investigation include: No exercise (BEHAVIORAL), Morning exercise (BEHAVIORAL), Evening exercise (BEHAVIORAL).

Who is sponsoring clinical trial NCT03019510?

This trial is sponsored by University of Missouri-Columbia, which has 291 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03019510's enrollment target sits among peer trials

54 1268th of 2000 higher than 730 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03019510, the US trial registry maintained by the National Library of Medicine. NCT03019510 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.