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Exercise Type That Faster Reduces Postprandial Glycemia.

Exercise Type That Faster Reduces Postprandial Glycemia.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04846751
Acronym
GLYEXER
Enrollment
11
Registered
2021-04-15
Start date
2021-11-01
Completion date
2024-09-10
Last updated
2022-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise-Induced Hyperinsulinism, Glucose, High Blood

Brief summary

It is well established that a bout of 50 min of continuous moderate intensity exercise, improves insulin sensitivity up to 48 hours after the bout. However, it is less well known, what is the exercise type more efficient to buffer the elevations in blood glucose elicited by carbohydrate ingestion. The purpose of this study is to elucidate if intervalic exercise is superior to continous on improving postprandial glycemic control.

Detailed description

Carbohydrate oxidation, glucose and insulin blood concentrations, isotopically measured rate of appearance of endogenous and exogenous glucose will be measured in 4 ocassions. Participants will undergo in a cross-over randomized fashion the following trials: 1. Exercise pedalling during 50 min at 60% of their VO2max followed by an oral glucose tolerance test (OGTT). 2. Exercise pedalling during 50 min in a hot environment (33ºC) at 60% of their VO2max followed by an oral glucose tolerance test (OGTT). 3. Exercise pedalling during 50 min using intervalic bouts averaging 60% of VO2max followed by an oral glucose tolerance test (OGTT). 4. No exercise, followed by an oral glucose tolerance test (OGTT).

Interventions

BEHAVIORALTYPE OF EXERCISE (OR REST)

continous exercise in normal temperature, continous exercise in hot environment, intervallic exercise in normal temperature.

Sponsors

University of Castilla-La Mancha
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Study composed of 4 trials, full-crossover, administered in a randomized order with the inclusion of a control trial.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Participant must be capable and willing to provide consent, understand, instructions and protocols. * Minimal fitness level to be able to complete 50 min of continous exercise at a moderate intensity.

Exclusion criteria

* Smokers * Pregnancy * Any non-controlled medical condition which could influence results or could be worsened by exercise

Design outcomes

Primary

MeasureTime frameDescription
Blood glucose concentration16 weeksIncremental area under the curve during the 120 min of the oral glucose tolerance test
Blood insulin concentration16 weeksIncremental area under the curve during the 120 min of the oral glucose tolerance test

Secondary

MeasureTime frameDescription
Carbohydrate oxidation16 weeksMeasured using indirect calorimetry
Turnover rate of endogenous and exogenous glucose16 weeksMeasured using isotopic tracers.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026