Effects of Snack Types on Acute Glucose and Insulin Response

January 16, 2026 updated by: San Diego State University
The purpose of the present study was to determine the effects of different type of snack consumption on postprandial satiety, glucose, insulin, antioxidant capacity and anxiety in healthy subjects.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

160

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • California
      • San Diego, California, United States, 92182-7251
        • Recruiting
        • School of Exercise and Nutritional Sciences, SDSU
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 55 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 18-55 years old

Exclusion Criteria:

  • Smoker
  • Pregnant woman
  • Required dietary supplement use
  • Required medication of metabolic disorders
  • Allergy to nuts or gluten (wheat)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Pretzels
Subjects consume pretzels to examine postprandial response
To examine postprandial responses of pretzel consumption
Experimental: Brazil nuts
Subjects consume Brazil nuts to examine postprandial response
To examine postprandial responses of Brazil nut consumption
Active Comparator: Potato chips
Subjects consume potato chips to examine postprandial response
To examine postprandial responses of potato chip consumption
Experimental: Mixed nuts
Subjects consume mixed nuts to examine postprandial response
To examine postprandial responses of mixed nut consumption
Active Comparator: White bread
Subjects consume white bread to examine postprandial response
To examine postprandial responses of white bread consumption
Experimental: Dried mango
Subjects consume dried mango to examine postprandial response
To examine postprandial responses of dried mango consumption
Experimental: Mango fruit
Subjects consume fresh mango to examine postprandial response
To examine postprandial responses of fresh mango consumption

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of Satiety
Time Frame: 0, 20, 40, 60, 90 and 120 minutes post snack consumption
Hunger feeling (appetite) will be examined using visual analog scale (0-10): 0 least and 10 greatest
0, 20, 40, 60, 90 and 120 minutes post snack consumption
Change of glucose level
Time Frame: 0 and 40 minutes post snack consumption
Blood will be collected by finger pricks and change of glucose level will be examined.
0 and 40 minutes post snack consumption
Change of insulin level
Time Frame: 0 and 40 minutes post snack consumption
Blood will be collected by finger pricks and change of insulin level will be examined
0 and 40 minutes post snack consumption
Change of anxiety feeling
Time Frame: 0 and 40 minutes post snack consumption
Anxiety feeling will examined using STAI (Spielberger Stasumte-Trait Anxiety Inventory) questionnaire (1-4): 1 least and 4 greatest, total summed score will be used.
0 and 40 minutes post snack consumption
Change of antioxidant level
Time Frame: 0 and 40 minutes post snack consumption
Blood will be collected by finger pricks and change of antioxidant level will be examined
0 and 40 minutes post snack consumption

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 15, 2018

Primary Completion (Estimated)

December 1, 2028

Study Completion (Estimated)

December 1, 2028

Study Registration Dates

First Submitted

April 25, 2019

First Submitted That Met QC Criteria

May 17, 2019

First Posted (Actual)

May 20, 2019

Study Record Updates

Last Update Posted (Actual)

January 21, 2026

Last Update Submitted That Met QC Criteria

January 16, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HS-2019-0094

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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