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NCT06694155Recruiting

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

Source: ClinicalTrials.gov · Last updated 6 Apr 2026

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
15 Nov 2024
Start date
15 Jan 2025
Primary completion date
1 Nov 2026
Lead sponsor
University of Arkansas
NCT number
NCT06694155

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 15 Jan 2025 to the primary completion date, 1 Nov 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of chemotherapy or radiation therapy for cancer in the 6 months prior to enrollment.
  • Currently receiving androgen (e.g., testosterone) or anabolic (e.g., GH, IGF-I) therapy.
  • Currently using corticosteroid medications (cortisone, hydrocortisone, prednisone, etc.).

Other illness

  • History of gastrointestinal bypass/reduction surgery.
  • History of a chronic inflammatory disease (e.g. Lupus, Crohn's disease)
  • Any medical condition or medication that the PI or clinical study staff finds contradictory to this study.

Lab values

  • Hemoglobin \<10g/dL at screening.

Other

  • 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.
  • Pregnant or lactating individuals.
  • Unwilling to avoid using protein or amino-acid supplements during participation.
  • Unwilling to fast overnight.

Who the study is looking for

  • 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

Age in the registry: 50 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Arkansas for Medical Sciences
Coordinator of this site? Confirm its status
Little RockUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.