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CompletedNCT03310476Updated Sep 16, 2019

Influence of Resistant Starch Intake in Potatoes on Blood Glucose and Satiety Responses in Overweight Females

An interventional study of Potatoes in Overweight and Obesity, sponsored by Texas Woman's University. Completed at 1 site in United States. Open to female participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-09-16.

Sponsored by Texas Woman's University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Female
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Overweight and Obesity

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03

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Overweight and obese (BMI between 28 and 40 kg/m\^2)
  • Any race or ethnicity

Exclusion criteria

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
04

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Baked, consumed chilled potatoes

    Other: Potatoes

  • Experimental
    Boiled, consumed hot potatoes

    Other: Potatoes

Interventions

  • OtherPotatoes

    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.

05

What researchers measure

Primary outcomes

  1. Change in postprandial glucose and insulin concentrations

    Postprandial glucose and insulin concentrations will be compared between interventions

    Time frame: Change in glucose and insulin concentrations collected 15, 30, 60, and 120 minutes following potato intake

Secondary outcomes

  1. Change in postprandial glucagon-like peptide- 1 (GLP-1, pg/mL) concentrations

    Postprandial changes in GLP-1 will be compared between interventions

    Time frame: Change in GLP-1 concentrations collected 15, 30, 60, and 120 minutes following potato intake

  2. Change in postprandial peptide YY (PYY, pg/mL) concentrations

    Postprandial changes in PYY will be compared between interventions

    Time frame: Change in PYY concentrations collected 15, 30, 60, and 120 minutes following potato intake

  3. Change in postprandial glucose-dependent insulinotropic peptide (GIP, pg/mL) concentrations

    Postprandial changes in GIP will be compared between interventions

    Time frame: Change in GIP concentrations collected 15, 30, 60, and 120 minutes folllowing potato intake

Other outcomes

  1. Change in postprandial subjective satiety

    Change in postprandial subjective satiety measured by Visual Analogue Scale (VAS) will be compared between interventions

    Time frame: VAS measured immediately and 120 minutes following potato intake

  2. Change in subsequent energy intake

    Change in subsequent energy intake 48 hours following potato intake will be compared between interventions

    Time frame: Subsequent energy intake over 48 hours following potato intake

06

Study locations

1 site
  • Texas Woman's University
    Houston, Texas 77030, United States
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03310476
Lead sponsor
Texas Woman's University
Collaborators
Alliance for Potato Research and Education
Responsible party
Mindy Patterson Maziarz (Assistant Professor, Texas Woman's University) — Principal investigator
First posted
Oct 16, 2017
Start date
Jan 1, 2018
Primary completion
Aug 31, 2019
Completion
Aug 31, 2019
Last update
Sep 16, 2019

Study contacts

Mindy Patterson, PhD, RDN
principal investigator · Texas Woman's University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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