- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03310476
Influence of Resistant Starch Intake in Potatoes on Blood Glucose and Satiety Responses in Overweight Females
September 12, 2019 updated by: Mindy Patterson Maziarz, Texas Woman's University
Influence of Resistant Starch in Baked and Boiled Potatoes on Glycemic and Satiety Responses in Overweight Females
Resistant starch (RS) is a type of fiber that has unique digestive properties that can impact overall health including glucose homeostasis and satiety.
RS found in potatoes can be increased by using certain cooking methods and serving temperatures.
The purpose of this trial will compare the acute glycemic and satiety responses after consuming potatoes differing in RS content that are 1) baked then chilled or 2) boiled and consumed hot in overweight females on two separate occasions.
Study Overview
Detailed Description
Potatoes are a low-cost, nutrient-dense dietary staple in the U.S. rich in complex carbohydrates, potassium, magnesium, and fiber, but low in fat and sodium.
Starch is the main complex carbohydrate found in potatoes that yields glucose to contribute to overall energy needs.
Another type of starch found in potatoes is resistant to amylase hydrolysis in the small intestine which is resistant starch (RS).
Trials using RS as a functional ingredient (~15-30 g/day) in healthy and overweight adults resulted in improvements in postprandial glucose, insulin sensitivity, satiety hormone response, and subjective satiety.
Limited data exists using RS naturally found in commonly consumed foods, such as potatoes.
Altering the cooking methods and serving temperatures of potatoes can influence the amount of RS to impact glucose, satiety hormone response, and subjective satiety.
Using a cross-sectional, cross-over design, the aim of this study will determine how potatoes 1) baked and chilled or 2) boiled and consumed hot influence postprandial glycemic parameters, satiety hormones (glucagon-like peptide-1, peptide YY, and glucose-dependent insulinotropic polypeptide), subjective satiety, and subsequent energy intake in overweight females.
Study Type
Interventional
Enrollment (Actual)
30
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 Locations
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Texas
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Houston, Texas, United States, 77030
- Texas Woman's University
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-
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
14 years to 36 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Overweight and obese (BMI between 28 and 40 kg/m^2)
- Any race or ethnicity
Exclusion Criteria:
- Diabetes or other metabolic disorder, cancer, or cardiovascular disease
- Smoking
- Pregnant or lactating
- More than 5% weight loss or gain over prior 6 months
- Following a special diet
- Sensitivity or aversion to potatoes
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Baked, consumed chilled potatoes
|
Participants will follow the same protocol for each arm with a minimum of 1-week wash-out period between arms.
For each arm, fasting blood will be collected then 200 g of potato will be consumed.
Postprandial blood will be collected 15, 30, 60, and 120 minutes.
Subjective satiety will be assessed using Visual Analogue Scale three times, as well as 48-hour subsequent dietary intake.
|
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Experimental: Boiled, consumed hot potatoes
|
Participants will follow the same protocol for each arm with a minimum of 1-week wash-out period between arms.
For each arm, fasting blood will be collected then 200 g of potato will be consumed.
Postprandial blood will be collected 15, 30, 60, and 120 minutes.
Subjective satiety will be assessed using Visual Analogue Scale three times, as well as 48-hour subsequent dietary intake.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in postprandial glucose and insulin concentrations
Time Frame: Change in glucose and insulin concentrations collected 15, 30, 60, and 120 minutes following potato intake
|
Postprandial glucose and insulin concentrations will be compared between interventions
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Change in glucose and insulin concentrations collected 15, 30, 60, and 120 minutes following potato intake
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in postprandial glucagon-like peptide- 1 (GLP-1, pg/mL) concentrations
Time Frame: Change in GLP-1 concentrations collected 15, 30, 60, and 120 minutes following potato intake
|
Postprandial changes in GLP-1 will be compared between interventions
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Change in GLP-1 concentrations collected 15, 30, 60, and 120 minutes following potato intake
|
|
Change in postprandial peptide YY (PYY, pg/mL) concentrations
Time Frame: Change in PYY concentrations collected 15, 30, 60, and 120 minutes following potato intake
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Postprandial changes in PYY will be compared between interventions
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Change in PYY concentrations collected 15, 30, 60, and 120 minutes following potato intake
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|
Change in postprandial glucose-dependent insulinotropic peptide (GIP, pg/mL) concentrations
Time Frame: Change in GIP concentrations collected 15, 30, 60, and 120 minutes folllowing potato intake
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Postprandial changes in GIP will be compared between interventions
|
Change in GIP concentrations collected 15, 30, 60, and 120 minutes folllowing potato intake
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in postprandial subjective satiety
Time Frame: VAS measured immediately and 120 minutes following potato intake
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Change in postprandial subjective satiety measured by Visual Analogue Scale (VAS) will be compared between interventions
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VAS measured immediately and 120 minutes following potato intake
|
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Change in subsequent energy intake
Time Frame: Subsequent energy intake over 48 hours following potato intake
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Change in subsequent energy intake 48 hours following potato intake will be compared between interventions
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Subsequent energy intake over 48 hours following potato intake
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Mindy Patterson, PhD, RDN, Texas Woman's University
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 1, 2018
Primary Completion (Actual)
August 31, 2019
Study Completion (Actual)
August 31, 2019
Study Registration Dates
First Submitted
September 21, 2017
First Submitted That Met QC Criteria
October 10, 2017
First Posted (Actual)
October 16, 2017
Study Record Updates
Last Update Posted (Actual)
September 16, 2019
Last Update Submitted That Met QC Criteria
September 12, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Resistant starch in potatoes
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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