Royal Ancient Oats™ Study

Recruiting now · Not applicable

Conditions studied: Healthy Participants, Healthy Glucose

In brief

Evaluating the effects of high avenanthramide ancient oat (Royal Ancient Oats™) muffins versus conventional oat muffins in regard to glycemic control.

Key facts

Study ID

NCT07371598

Run by

Standard Process Inc.

People needed

38

Starts

2026-01-13

Expected to finish

2026-09-15

Last updated by the study team

2026-01-28

Who can join

Age: 35 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Non-diabetic (HbA1c<5.7%) adults both men and women between the ages of 35-65 years with body mass index (BMI) ranging from 25 to 30 kg/m2
• Participants who meet the inclusion criteria will be screened prior to starting the study and must be able to adhere to the requirements of the study.
• Willing to comply with study procedures and supplement regimens.
• Providing consent to participate in the study.
• Willing to limit/minimize foods that are rich sources of fiber and high carb content.
• Participants should avoid taking any non-prescription/over-the-counter medications or nutritional supplements that could influence glycemic response. This includes vitamins, herbal supplements, and any medications affecting metabolism. Examples include probiotics and prebiotics, vit D, vit B12, Ginseng, fenugreek, weight loss supplements like green tea extract and Garcinia cambogia, fiber supplements like inulin and Psyllium husk. If participants need to make any changes due to health reasons, they should consult with the study coordinator before doing so.

You may not qualify if…

• Participants who have experienced weight loss or gain exceeding 5% of their body weight in the past 3 months, including those involved in any weight loss or weight gain programs through diet and/or lifestyle changes.
• Participants currently taking medications that could alter metabolism, such as weight loss medications, anti-hypertensive drugs, or lipid-lowering medications.
• Participants with any chronic metabolic diseases, including diabetes, or those using supplements other than a daily multivitamin.
• Pregnant or lactating women will be excluded from the study.
• Participants who use tobacco products.
• Participants who are unwilling to limit or minimize foods that are rich sources of fiber and high carbohydrate content.
• Excessive alcohol consumption (e.g., more than two drinks per day for men and more than one drink per day for women)
• Inconsistency in recent or planned changes in non-prescription/over-the-counter medications or nutritional supplements affecting glycemic response, including vitamins (e.g., Vitamin D, Vitamin B12), herbal supplements (e.g., Ginseng, Fenugreek), weight loss supplements (e.g., green tea extract, Garcinia cambogia), fiber supplements (e.g., inulin, psyllium husk), and probiotics/prebiotics.
• Inability or unwillingness to maintain the current regimen of these medications and supplements throughout the study period without consulting the study coordinator.

Where it is running

• Standard Process Nutrition Innovation Center — Kannapolis, North Carolina, United States (enrolling)

Full record on ClinicalTrials.gov

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