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Acute Metabolic Effects of Pre-meal Consumption of Whey in Women at Risk of Gestational Diabetes Mellitus

Primary Purpose

Gestational Diabetes Mellitus in Pregnancy

Status
Active
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Whey
Placebo
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gestational Diabetes Mellitus in Pregnancy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Referred to screening for Gestational Diabetes Mellitus by week 24-30
  • BMI 20-35
  • Normal blood pressure
  • Age > 18 years

Exclusion Criteria:

  • Special dietary regimes > 1 month at time of inclusion e.g. ketogenic diet
  • Daily intake of protein supplements
  • Milk allergy or phenylketonuria
  • Celiac disease
  • Medication with effect on glucose metabolism e.g. steroid
  • Do not speak or understand Danish
  • Gemelli
  • Polycystic Ovarian Syndrome
  • PI finds the patient unfit (like mental illness, too nervous or other)
  • Anemia (hemoglobin <6 mmol/l)
  • Severe chronic illness
  • Depression
  • Severe nausea/vomiting
  • Non-breakfast eaters

Sites / Locations

  • Medicinsk forskningslaboratorium for Diabetes og Hormonsygdomme og Steno Diabetes Center Aarhus (M-lab), Aarhus universitetshospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Whey

Placebo

Arm Description

Whey protein isolate WPI (Lacprodan® ISO.Water. from Arla Foods Ingredients). The intervention will be ingested 30 min. prior to an OGTT (3 hours). The intervention will also be ingested 30 min prior to breakfast in the women's own environment.

The placebo will be ingested 30 min. prior to an OGTT (3 hours). The placebo will also be ingested 30 min prior to breakfast in the women's own environment.

Outcomes

Primary Outcome Measures

Concentration differences in blood glucose following an OGTT

Secondary Outcome Measures

Concentration differences in glucose independent peptide (GIP)
Concentration differences in glucagon like peptide 1 (GLP-1)
Concentration differences in glucagon
Concentration differences in insulin
Concentration differences in c-peptide
Concentration differences in free fatty acids (FFA)
Concentration differences in ghrelin
Concentration differences in leptin
Concentration differences in amino acids (AA)
Gastric emptying rate (Concentration differences in blood paracetamol/acetaminophen)
Resting energy expenditure (REE) (Resting Metabolic Rate)
Respiratory quotient (RQ)
Self-reported appetite
A visual analogue scale ranging from "not at all" to "extremely" will be used to assess Hunger, Fullness, Satiety, Desire, Prospective consumption (Quantity).
Heart rate
A combined accelerometer and heart rate monitor will be used to measure heart rate (beats/minute)
Energy expenditure
A combined accelerometer and heart rate monitor will be used to estimate energy expenditure (kCal)
Activity
A combined accelerometer and heart rate monitor will be used to measure activity (counts/minute)
Continuous glucose measurements (CGM)
Time in range, concentration differences in interstitial fluid glucose 3 hours following breakfast, glycemic variability, mean glucose, daily maximum glucose, estimated HbA1c

Full Information

First Posted
February 12, 2021
Last Updated
April 18, 2023
Sponsor
University of Aarhus
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1. Study Identification

Unique Protocol Identification Number
NCT04767880
Brief Title
Acute Metabolic Effects of Pre-meal Consumption of Whey in Women at Risk of Gestational Diabetes Mellitus
Official Title
Acute Metabolic Effects of Pre-meal Consumption of Whey in Women at Risk of Gestational Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 26, 2021 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
October 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The main objective of our study is to investigate the metabolic effects of whey protein (whey protein isolate, WPI, (Lacprodan® ISO.Water. from Arla Foods Ingredients) compared to placebo when consumed by women in risk of gestational diabetes mellitus (GMD) 30 minutes prior to an oral glucose tolerance test (OGTT). We will also investigate any changes in substrate metabolism and energy expenditure using indirect calorimetry. Differences in hunger and satiety parameters as well as rate of gastric emptying will also be assessed. Furthermore, we will investigate the glucose response when the women consume the intervention at home in their own environment 30 minutes before breakfast in various doses (placebo, 10, 15, 20, 30 g whey). The women will be monitored with continuous glucose monitors, activity monitors and all meals will be provided. The two study days in the laboratory will be repeated 3-9 months after pregnancy. The purpose of this is to be able to compare the metabolic response of pre-meal whey during pregnancy with the response in a not-pregnant state. The study days at home will not be repeated after pregnancy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes Mellitus in Pregnancy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Singleblind, randomized, crossover design
Masking
Participant
Masking Description
Participants will be blinded to the intervention and placebo in the laboratory setting. Quadruple (Participants, care providers, investigators and outcome assessors) Participants, care providers, investigators and outcome assessors will be blinded to the placebo and varying doses of whey in the home setting.
Allocation
Randomized
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Whey
Arm Type
Experimental
Arm Description
Whey protein isolate WPI (Lacprodan® ISO.Water. from Arla Foods Ingredients). The intervention will be ingested 30 min. prior to an OGTT (3 hours). The intervention will also be ingested 30 min prior to breakfast in the women's own environment.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
The placebo will be ingested 30 min. prior to an OGTT (3 hours). The placebo will also be ingested 30 min prior to breakfast in the women's own environment.
Intervention Type
Dietary Supplement
Intervention Name(s)
Whey
Intervention Description
Doses of 10, 15, 20 and 30 gram protein of a regular whey protein compound (whey protein isolate WPI (Lacprodan® ISO.Water. from Arla Foods Ingredients))
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
The placebo contains <1 kcal and 0 g protein
Primary Outcome Measure Information:
Title
Concentration differences in blood glucose following an OGTT
Time Frame
3 hours following the OGTT
Secondary Outcome Measure Information:
Title
Concentration differences in glucose independent peptide (GIP)
Time Frame
3 hours following the OGTT
Title
Concentration differences in glucagon like peptide 1 (GLP-1)
Time Frame
3 hours following the OGTT
Title
Concentration differences in glucagon
Time Frame
3 hours following the OGTT
Title
Concentration differences in insulin
Time Frame
3 hours following the OGTT
Title
Concentration differences in c-peptide
Time Frame
3 hours following the OGTT
Title
Concentration differences in free fatty acids (FFA)
Time Frame
3 hours following the OGTT
Title
Concentration differences in ghrelin
Time Frame
3 hours following the OGTT
Title
Concentration differences in leptin
Time Frame
3 hours following the OGTT
Title
Concentration differences in amino acids (AA)
Time Frame
3 hours following the OGTT
Title
Gastric emptying rate (Concentration differences in blood paracetamol/acetaminophen)
Time Frame
3 hours following the OGTT
Title
Resting energy expenditure (REE) (Resting Metabolic Rate)
Time Frame
3 hours following the OGTT
Title
Respiratory quotient (RQ)
Time Frame
3 hours following the OGTT
Title
Self-reported appetite
Description
A visual analogue scale ranging from "not at all" to "extremely" will be used to assess Hunger, Fullness, Satiety, Desire, Prospective consumption (Quantity).
Time Frame
3 hours following the OGTT and 3 hours following breakfast
Title
Heart rate
Description
A combined accelerometer and heart rate monitor will be used to measure heart rate (beats/minute)
Time Frame
5 days
Title
Energy expenditure
Description
A combined accelerometer and heart rate monitor will be used to estimate energy expenditure (kCal)
Time Frame
5 days
Title
Activity
Description
A combined accelerometer and heart rate monitor will be used to measure activity (counts/minute)
Time Frame
5 days
Title
Continuous glucose measurements (CGM)
Description
Time in range, concentration differences in interstitial fluid glucose 3 hours following breakfast, glycemic variability, mean glucose, daily maximum glucose, estimated HbA1c
Time Frame
5 days

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Referred to screening for Gestational Diabetes Mellitus by week 24-30 or GDM BMI 20-35 Normal blood pressure Age > 18 years Exclusion Criteria: Special dietary regimes > 1 month at time of inclusion e.g. ketogenic diet Daily intake of protein supplements Milk allergy or phenylketonuria Celiac disease Medication with effect on glucose metabolism e.g. steroid Do not speak or understand Danish Gemelli Polycystic Ovarian Syndrome PI finds the patient unfit (like mental illness, too nervous or other) Anemia (hemoglobin <6 mmol/l) Severe chronic illness Depression Severe nausea/vomiting Non-breakfast eaters
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Per G Ovesen, Professor
Organizational Affiliation
Institute of Clinical Medicine, Aarhus University and Department of Gynecology and Obstetrics and Steno Diabetes Center Aarhus, Aarhus University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Medicinsk forskningslaboratorium for Diabetes og Hormonsygdomme og Steno Diabetes Center Aarhus (M-lab), Aarhus universitetshospital
City
Aarhus
Country
Denmark

12. IPD Sharing Statement

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Acute Metabolic Effects of Pre-meal Consumption of Whey in Women at Risk of Gestational Diabetes Mellitus

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