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Mealtime Walking Study to Improve Postprandial Metabolic Response

Mealtime Walking Study to Improve Postprandial Metabolic Response

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04499287
Enrollment
10
Registered
2020-08-05
Start date
2014-09-17
Completion date
2015-03-10
Last updated
2021-07-23

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

Conditions

PreDiabetes, Postprandial Hyperglycemia

Keywords

blood glucose, blood insulin, fiber, prediabetes, postprandial glycemia

Brief summary

This randomized crossover trial will investigate the metabolic responses following the consumption of a bagel+juice meal under 3 conditions: control, fiber (positive control), and postmeal walk in15 healthy adults. It is hypothesized that the postmeal walk will reduce glycemia, insulinemia, and oxidative stress similar to fiber.

Detailed description

The study will follow a randomized, crossover design. Participants and the investigator will be blinded for the control treatments but not for the walk treatment. Participants will complete 3 meal tests; tests are separated by about 1 week. An initial screening visit will be scheduled for the online survey respondents that meet the inclusion criteria and are willing to consider participation. At this visit, written consent will be secured followed by further screening for the exclusion criteria and the collection of demographic and health history data and anthropometric measures. A fasting blood sample will be collected for glucose analysis. Participants will be scheduled for experimental testing and provided with instructions and calendars. Participants will be given at least one week's notice if they do not qualify for the trial based on fasting glucose concentrations. On the day prior to each experimental day, the participants will consume 2 bagels (54 g carbohydrate/bagel), and on the night prior to each visit, participants will consume a standard dinner of their choice. (The bagels will be provided to participants and the standardized dinner will be documented. The bagels and standardized dinner meal will facilitate controlled 'glycogen loading' prior to testing.) No other food will be consumed after this dinner meal, and participants will fast overnight until they arrive at the research center the next morning (e.g., no food or beverage with the exception of water). Fasting blood (1 tablespoon) will be collected and the test meal (bagel+juice) will be consumed. Postprandial blood samples will be collected for 4 hours (see below). The subjects will not be allowed to consume any food or beverage (with the exception of water) through the duration the visit. A snack will be provided to participants once the testing is over. Glucose: 0,15,30,60,120, 180, 240 Insulin: 0, 30, 120, 180, 240 Oxidative Stress Markers: 0, 180, 240 The blood insulin level will be determined in venous blood by RIA. Capillary blood glucose will be determined with a glucometer. Oxidative stress, e.g., total antioxidant capacity, IL-6, and TBARS will be assessed using microplate analyses kits.

Interventions

OTHER15-minute walk at preferred walking speed.
DIETARY_SUPPLEMENTFiber

9 grams soluble fiber

OTHERcontrol

control

Sponsors

Arizona State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Intervention model description

randomized, controlled, crossover

Eligibility

Sex/Gender
ALL
Age
35 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* obese (BMI ≥ 30 kg/m2) * nonsmoking * sedentary * fasting capillary blood glucose that measured from 5.6 to 6.9 mmol/L

Exclusion criteria

* answered yes to any of the questions on the Par-Q & You questionnaire * refused to discontinue antioxidant supplement use for several weeks prior to and during the study * prescribed medication use (unless use was consistent for the 3 months prior to the study and intake remained consistent throughout the study duration) * food allergies or medical conditions that impacted normal functioning of the gastrointestinal tract

Design outcomes

Primary

MeasureTime frameDescription
Postprandial glycemia4 hoursincremental area under curve
postprandial insulinemia4 hoursincremental area under curve

Secondary

MeasureTime frameDescription
postprandial oxidative stress4 hourstotal antioxidant capacity of blood

Outcome results

None listed

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