Effect of White Potatoes on Glycemic Response and Satiety in Older Adults

Sponsor
Ryerson University (Other)
Overall Status
Completed
CT.gov ID
NCT03309124
Collaborator
(none)
20
1
5
15.7
1.3

Study Details

Study Description

Brief Summary

The purpose of the present study is to explore the influence of cooking methods of potatoes on post-prandial glycaemia and satiety in healthy older adults.

Condition or Disease Intervention/Treatment Phase
  • Other: White bread
  • Other: Baked potato with skin
  • Other: Mashed potatoes
  • Other: Fried French fries
  • Other: Meal skipping
N/A

Detailed Description

Each of the 5 study sessions will be at least 7 days apart. Either meal skipping, or one of three treatments of white potatoes (a) baked (with skin), (b) mashed, (c) fried French fries, or white bread, prepared on the day of testing, will be served to healthy older adults (65+ years). Participants will consume the equivalent to 1 medium sized potato (~280 kcal) or an equivalent amount of calories from white bread. Glycemic response, insulin, incretin hormones (glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic peptide (GIP)), dipeptidyl peptidase 4 (DPP4), and cholecystokinin (CCK) will be measured for 2 h (0, 15, 30, 45, 60, 90 and 120 min) following meal consumption, as well as mood and subjective appetite. An ad libitum test meal will be provided at 120 min to assess food intake suppression.

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Effect of White Potatoes on Glycemic Response and Satiety in Older Adults
Actual Study Start Date :
Apr 9, 2018
Actual Primary Completion Date :
Aug 1, 2019
Actual Study Completion Date :
Aug 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: White bread

Matched for energy content and available carbohydrate content of potato treatments

Other: White bread
Toasted, with canola oil added to match for fat content of French fries (13.9 grams), as well as being matched for energy (280 kilocalories) and available carbohydrate content (33 grams) of potato treatments.

Experimental: Baked potato with skin

Baked russet potato

Other: Baked potato with skin
Baked russet potato with canola oil added once baked to match for fat content of French fries, and also matched for the salt content of white bread (280 milligrams).

Experimental: Mashed potatoes

Mashed potatoes prepared from frozen, matched for available carbohydrate content of baked potato

Other: Mashed potatoes
Mashed potatoes prepared from frozen, with canola oil added to match for fat content of French fries, as well as being matched for energy and available carbohydrate content of the baked potato.

Experimental: Fried French fries

Matched for available carbohydrate content of baked potato

Other: Fried French fries
Prepared from frozen, matched for energy and available carbohydrate content of baked potato and salt content of white bread.

Experimental: Meal skipping

No food given

Other: Meal skipping
No food given

Outcome Measures

Primary Outcome Measures

  1. Ad libitum food intake (lunch, at 120 minutes) [120 minutes after meal consumption]

    Food intake will be determined by weighing the meal before and after serving. The net weight of the test meal will be converted to calories

  2. Change from baseline glycemic response [baseline and then 15, 30, 45, 60, 90 and 120 minutes after meal consumption]

    Blood glucose (mmol/L). Blood glucose will be measured in whole blood using YSI 2300 STAT PLUS (YSI Incorporated, Yellow Springs, OH)

  3. Change from baseline insulin [baseline and then 15, 30, 45, 60, 90 and 120 minutes after meal consumption]

    Blood insulin (pmol/L). Insulin concentration in serum will be determined in duplicate via enzyme-linked immunosorbent assay kits (ELISA; Millipore, Billerica, Massachusetts).

Secondary Outcome Measures

  1. Change from baseline subjective appetite [baseline and then 15, 30, 45, 60, 90 and 120 minutes after meal consumption]

    Measured using visual analogue scale (mm). Each VAS is a 100 mm line where they will place a pencil mark to describe their feelings.

  2. Change from baseline mood [baseline and then 15, 30, 45, 60, 90 and 120 minutes after meal consumption]

    Measured using visual analogue scale (mm). Each VAS is a 100 mm line where they will place a pencil mark to describe their feelings.

  3. Change from baseline cholecystokinin (CCK) [baseline and then 15, 30, 45, 60, 90 and 120 minutes after meal consumption]

    Blood CCK (pmol/L). CCK concentration in serum will be determined in duplicate via enzyme-linked immunosorbent assay kits (ELISA; Millipore, Billerica, Massachusetts)

  4. Change from baseline dipeptidyl peptidase 4 (DPP4) [baseline and then 15, 30, 45, 60, 90 and 120 minutes after meal consumption]

    Blood DPP4 (ng/mL). DPP4 concentration in serum will be determined in duplicate via enzyme-linked immunosorbent assay kits (ELISA; Millipore, Billerica, Massachusetts)

  5. Change from baseline glucose-dependent insulinotropic peptide (GIP) [baseline and then 15, 30, 45, 60, 90 and 120 minutes after meal consumption]

    Blood GIP (pmol/L). GIP concentration in serum will be determined in duplicate via enzyme-linked immunosorbent assay kits (ELISA; Millipore, Billerica, Massachusetts)

  6. Change from baseline glucagon-like peptide-1 (GLP-1) [baseline and then 15, 30, 45, 60, 90 and 120 minutes after meal consumption]

    Blood GLP-1 (pmol/L). GLP-1 concentration in serum will be determined in duplicate via enzyme-linked immunosorbent assay kits (ELISA; Millipore, Billerica, Massachusetts)

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • be 65 years or older

  • be healthy

  • not be taking medications that affect food intake regulation or blood glucose

Exclusion Criteria:
  • anyone with food sensitivities or allergies to potatoes or potato-products,

  • smokers

  • diabetic or overweight/obese individuals.

Contacts and Locations

Locations

Site City State Country Postal Code
1 School of Nutrition, Ryerson University Toronto Ontario Canada M5B 2K3

Sponsors and Collaborators

  • Ryerson University

Investigators

  • Principal Investigator: Nick Bellissimo, PhD, Ryerson University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nick Bellissimo, Associate Professor, Ryerson University
ClinicalTrials.gov Identifier:
NCT03309124
Other Study ID Numbers:
  • REB2017-330
First Posted:
Oct 13, 2017
Last Update Posted:
Sep 13, 2019
Last Verified:
Sep 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Nick Bellissimo, Associate Professor, Ryerson University

Study Results

No Results Posted as of Sep 13, 2019