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NCT06025292 · University of Arkansas

Effects of Lean Pork Loin Intake on Protein Homeostasis and Glucose Regulation in Prediabetic Adults

(PORK)

What this study is about

We will be directly comparing a high-quality protein diet composed primarily of lean pork loin (PORK) to a lower-quality plant-based protein diet (PLANT) in individuals with prediabetes on muscle and whole-body protein turnover and glucose regulation.

View original scientific description

We will be directly comparing a high-quality protein diet composed primarily of lean pork loin (PORK) to a lower-quality plant-based protein diet (PLANT) in individuals with prediabetes on muscle and whole-body protein turnover and glucose regulation.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • 1\. Males and females ages 40-65 years.
  • 2\. BMI 25 to ≤40 kg/m2 (or body fat % ≥25% in males or ≥36% in females)
  • 3\. Capable of providing informed consent.
  • 4\. COVID-19 negative and/or asymptomatic.
  • 5\. Willing to abstain from drinking alcohol or consuming marijuana and CBD products during the 4-day study meal period
  • 6\. HbA1c: 5.7-6.4% or fasting glucose 100-125 mg/dL

Exclusion criteria

  • 1\. Participant who does not/will not eat animal protein sources.
  • 2\. Allergy to wheat, soy, or common ingredients in plant-based protein products.
  • 3\. Body mass index \<25 kg/m2 or \>40 kg/m2.
  • 4\. Hemoglobin \<10g/dL at screening.
  • 5\. Platelets \<150,000/uL at screening.
  • 6\. History of chemotherapy or radiation therapy for cancer in the 6 months prior to enrollment.
  • 7\. History of gastrointestinal bypass/reduction surgery.
  • 8\. Pregnant or lactating individuals.
  • 9\. History of a chronic inflammatory disease (e.g. Lupus, Crohn's disease)
  • 10\. Currently receiving androgen (e.g., testosterone) or anabolic (e.g., GH, IGF-I) therapy.
  • 11\. Currently using prescription blood thinning medications.
  • 12\. Currently using corticosteroid medications (cortisone, hydrocortisone, prednisone, etc.).
  • 13\. Unable or unwilling to suspend aspirin use for 7 days prior to Visit 3 and Visit 7.
  • 14\. Unwilling to avoid using protein or amino-acid supplements during participation.
  • 15\. Unwilling to fast overnight.
  • 16\. Unwilling to avoid alcohol, marijuana and CBD products for the four study days.
  • 17\. Participants on glucagon-like-peptide-1 receptor agonist (GLP-1-RA) medications for \<1 month or with less than one treatment dose (injection) every two weeks

Where

  • Little Rock, Arkansas

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Jun 8, 2026 · Source of record for eligibility and locations

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1 of 20 participants interested
5% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

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Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

Little Rock

Arkansas

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Hyperglycaemia (Non Diabetic) Treatment in Little Rock?

Join others in Arkansas exploring innovative treatment options through clinical research

Hyperglycaemia (Non Diabetic) Treatment Options in Little Rock, Arkansas

If you're searching for Hyperglycaemia (Non Diabetic) treatment in Little Rock, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Little Rock and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Hyperglycaemia (Non Diabetic). All study-related care is provided at no cost to participants.

Local Sites
1 locations in Arkansas
Now Enrolling
Up to 20 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Hyperglycaemia (Non Diabetic)?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Hyperglycaemia (Non Diabetic)

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Hyperglycaemia (Non Diabetic) Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT06025292. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.