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NCT Number: NCT06694155

Whey Protein Ingestion and Glucose Control in Pre- and Post Diabetic Individuals

To examine the effects of twice daily whey protein consumption on blood glucose and insulin in pre-diabetic and diabetic individuals

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Key information

Age range

50 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Arkansas for Medical Sciences

Little Rock, Arkansas, 72202, United States

Location status: Recruiting

Location contact

Samantha Seale, MS

CONTACT

[email protected]

501-320-7602

About this study

Protein consumption in the morning has been shown to reduce appetite and caloric intake (19). In addition, premeal whey consumption reduces post prandial blood glucose, reduces gastric emptying rate, and increases peak blood insulin (10). Thus, it is proposed that ingestion of whey protein within 1hr of waking (and prior to breakfast) and 30 minutes prior to dinner will be more effective in suppressing appetite, carbohydrate intake, and glucose AUC. Ingestion upon waking will mitigate the cortisol-induced drive for carbohydrate intake. Ingestion prior to dinner, the most frequently consumed and largest meal in America (20), will reduce food intake, post meal blood glucose, and insulin area under the curve (21).

Specific Aims

  • Determine the effect of WP ingestion within 1hr of waking and prior to breakfast, and 30min prior to dinner, on appetite suppression, carbohydrate and caloric intake, and 24hr glucose AUC over 7d in pre-diabetic (A1C 5.7%-6.4%) and diabetic (A1C 6.5%-7.5%) individuals.
  • Determine the effect of WP ingestion within 1hr of waking and 30min prior to dinner on changes in OGTT, Matsuda index, and whole-body protein balance (compared to control) before and after 7d of WP consumption in pre-diabetic and diabetic individuals.
  • Determine outcome differences between pre-diabetic and diabetic individuals.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males and females ages 50-70 years.
  • Body mass index between 25-45 kg/m2
  • Capable of providing informed consent.
  • COVID-19 negative and/or asymptomatic.
  • Willing to abstain from drinking alcohol or consuming marijuana and CBD products during the 7-day study meal period on two occasions.
  • HbA1c: 5.7-6.4% or 6.5% to 7.5% or fasting glucose ≥100 mg/dL

Exclusion criteria

  • Subject who does not/will not eat dairy protein sources.
  • Subjects taking exogenous insulin injections or GLP /GIP injections or other appetite suppressants.
  • Unwilling to keep a detailed 7 day food journal on two occasions
  • Unwilling to wear a CGM for 7 days on two occasions and share the data with the research team.
  • Lactose intolerance.
  • Hemoglobin <10g/dL at screening.
  • History of chemotherapy or radiation therapy for cancer in the 6 months prior to enrollment.
  • History of gastrointestinal bypass/reduction surgery.
  • Pregnant or lactating individuals.
  • History of a chronic inflammatory disease (e.g. Lupus, Crohn's disease)
  • Currently receiving androgen (e.g., testosterone) or anabolic (e.g., GH, IGF-I) therapy.
  • Currently using corticosteroid medications (cortisone, hydrocortisone, prednisone, etc.).
  • Unwilling to avoid using protein or amino-acid supplements during participation.
  • Unwilling to fast overnight.
  • Any medical condition or medication that the PI or clinical study staff finds contradictory to this study.

Treatment and study plan

Whey Protein Isolate Crossover

Dietary Supplement

This crossover intervention includes 1 week of whey protein isolate supplementation and 1 week of placebo supplementation.

Placebo

Dietary Supplement

1 week of Non-whey protein Placebo supplement

Primary outcomes

  1. Whole body protein turnover

    Time frame: 7 days

    Whole body protein turnover reflects the continual synthesis and breakdown of body proteins. It can be measured at a whole-body or tissue level using stable isotope methods.

  2. Oral Glucose Tolerance Test

    Time frame: 7 days

    Oral Glucose Tolerance Test (OGTT) is used to screen for or diagnose diabetes. Normal blood values for a 75 gram OGTT are: Fasting -- 60 to 99 mg/dL (3.3 to 5.5 mmol/L), 1 hour -- Less than 200 mg/dL (11.1 mmol/L), 2 hours -- Less than 140 mg/dL (7.8 mmol/L) is normal.

  3. Blood glucose

    Time frame: 7 days

    Continuous glucose monitoring means using a device to automatically estimate your blood glucose level, also called blood sugar, throughout the day and night for 7 days.

Secondary outcomes

  1. Composite Appetite Scale

    Time frame: 7 days

    A composite appetite scale is a measure used to assess appetite control and influence energy intake. It can be calculated based on factors such as hunger, desire to eat, and fullness rating.

    Appetite Scale:

    How Hungry do you feel? Not Hungry at all <---> Have never been more Hungry How Satisfied do you feel? Completely empty <----> Can't eat another bite How Full do you feel? Not full at all <----> Totally full The more a person is satisfied and feels full and less hungry, the better the outcome is for whey vs placebo supplementation.

  2. Dietary Intake Log

    Time frame: 7 days

    A dietary intake log, also known as a food diary, is a self-reported account of all foods and beverages consumed within a specific timeframe.

Study contacts

Contact information is provided by the study sponsor or research team.

Arny Ferrando, PhD

CONTACT

[email protected]

5015265711

Sponsors and collaborators

Lead sponsor

University of Arkansas

Other

Collaborators

  • National Dairy Council

Registry information

Acronym: DAIRY

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Nov 19, 2024
Registry last updated
Apr 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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