- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03956602
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
Status
Recruiting
Conditions
Intervention / Treatment
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
- Name: Mee Young Hong
- Phone Number: 6195942392
- Email: mhong2@sdsu.edu
Study Locations
-
-
California
-
San Diego, California, United States, 92182-7251
- Recruiting
- School of Exercise and Nutritional Sciences, SDSU
-
Contact:
- Mee Young Hong
- Phone Number: 619-594-2392
- Email: mhong2@mail.sdsu.edu
-
-
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.
Sponsor
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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