Mealtime Walking Study to Improve Postprandial Metabolic Response

NCT ID: NCT04499287

Last Updated: 2021-07-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-09-17

Study Completion Date

2015-03-10

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

PreDiabetes Postprandial Hyperglycemia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

randomized, controlled, crossover
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Control

Test meal \[bagel with butter (20 g) and apple juice (240 ml) with added sugar (24 g)\] The meal was a total of 640 kcal (100 g carbohydrate, 21 g fat, 10 g protein. Participants remained seated in the laboratory with minimal activity for the four hours following test meal consumption. One week later the test meal was consumed with fiber (36 g, Metamucil powder, Procter\&Gamble, Cincinnati, OH) added to the apple juice (active) and participants remained seated in the laboratory with minimal activity for the four hours following test meal consumption . One week later participants were given 5 minutes to transition to the treadmill following consumption of the test meal and began walking on a motorized treadmill at their calculated preferred walking speed for 15 minutes (experimental). Afterwards participants remained seated in the laboratory with minimal activity for the remainder of the four hours following test meal consumption

Group Type PLACEBO_COMPARATOR

15-minute walk at preferred walking speed.

Intervention Type OTHER

Fiber

Intervention Type DIETARY_SUPPLEMENT

9 grams soluble fiber

control

Intervention Type OTHER

control

Fiber

Test meal \[bagel with butter (20 g) and apple juice (240 ml) with added sugar (24 g)\] The meal was a total of 640 kcal (100 g carbohydrate, 21 g fat, 10 g protein. 9 grams of soluble viscous fiber from psyllium husk (36 g, Metamucil powder, Procter\&Gamble, Cincinnati, OH) was mixed with the apple juice. Participants remained seated in the laboratory with minimal activity for the four hours following test meal consumption. One week later participants were given 5 minutes to transition to the treadmill following consumption of the test meal and began walking on a motorized treadmill at their calculated preferred walking speed for 15 minutes (experimental). Afterwards participants remained seated in the laboratory with minimal activity for the remainder of the four hours following test meal consumption. One week later the test meal was consumed, and participants remained seated in the laboratory with minimal activity for the four hours following test meal consumption (placebo).

Group Type ACTIVE_COMPARATOR

15-minute walk at preferred walking speed.

Intervention Type OTHER

Fiber

Intervention Type DIETARY_SUPPLEMENT

9 grams soluble fiber

control

Intervention Type OTHER

control

Walk

Test meal \[bagel with butter (20 g) and apple juice (240 ml) with added sugar (24 g)\] The meal was a total of 640 kcal (100 g carbohydrate, 21 g fat, 10 g protein. Participants were given 5 minutes to transition to the treadmill following consumption of the test meal and began walking on a motorized treadmill at their calculated preferred walking speed for 15 minutes. Afterwards participants remained seated in the laboratory with minimal activity for the remainder of the four hours following test meal consumption One week later the test meal was consumed, and participants remained seated in the laboratory with minimal activity for the four hours following test meal consumption (placebo comparator). One week later the test meal was consumed with fiber (36 g, Metamucil powder, Procter\&Gamble, Cincinnati, OH) added to the apple juice and participants remained seated in the laboratory with minimal activity for the four hours following test meal consumption (active comparator).

Group Type EXPERIMENTAL

15-minute walk at preferred walking speed.

Intervention Type OTHER

Fiber

Intervention Type DIETARY_SUPPLEMENT

9 grams soluble fiber

control

Intervention Type OTHER

control

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

15-minute walk at preferred walking speed.

Intervention Type OTHER

Fiber

9 grams soluble fiber

Intervention Type DIETARY_SUPPLEMENT

control

control

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

35 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Arizona State University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Carol Johnston

Professor and Associate Dean

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

OxPMW

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Ordered Eating and Acute Exercise
NCT06242015 COMPLETED NA
Breakfast Meal Replacement
NCT02482545 COMPLETED NA
Medifast 5 & 1 Plan
NCT01211301 COMPLETED NA
The Mixed Meal Challenge Study
NCT05087823 COMPLETED NA
Exercise and Weight Control
NCT02152501 COMPLETED NA
Food As MedicinE for Diabetes
NCT04828785 ACTIVE_NOT_RECRUITING NA