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Study identifier: NCT06861153 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Pulses: Optimizing Pulse Consumption for Cardiometabolic Health

Condition: Cardiovascular (CV) Risk · Healthy Eating Index · HbA1c  ·  Sponsor: University of Arizona

PhaseNA
Planned participants180
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersYes

About this study

This randomized clinical trial aims to evaluate the effects of consuming two different doses of pulses (1.5 cups/week or 3 cups/week) in individuals with baseline intake below 1.5 cups/week, compared to a control group receiving standard nutrition education based on the United States Department of Agriculture's (USDA) My Plate guidelines. The main question the Pulses study aims to answer is: • What is the effect of increasing pulse consumption (in a dose-response manner) on specific cardiometabolic risk factors, including LDL-C, CRP, HBA1C, and blood pressure compared to standard nutrition education? For secondary outcomes, this study aims to answer the following: • Does increased pulse consumption improve the following: overall serum lipid profile (Total cholesterol (TC), HDL-C, Triglycerides (TG), diet quality (measured by the Healthy Eating Index), and participants self-reported satisfaction with life (SWLS) and Satisfaction with Food-related Life (SWFoL). All participants will attend biweekly classes and food demonstrations. The pulses groups will learn to prepare various pulse-based recipes, while the control group will receive guidance on preparing healthy meals following the USDA MyPlate recommendations.

This description comes directly from the study's public registry record.

Talk to the study team

Kenneth Wilud, PhD  ·  520-626-3718  ·  kwilund@arizona.edu

Milad Hasankhani  ·  5208525064  ·  miladh@arizona.edu

Always discuss trial participation with your own doctor first.

Locations (2)

Tucson Village FarmTucson, Arizona, United StatesNot Yet Recruiting
University of ArizonaTucson, Arizona, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06861153