Overview

Cardiometabolic Effects of Pecans as a Snack

Status:
Not yet recruiting
Trial end date:
2026-06-01
Target enrollment:
0
Participant gender:
All
Summary
A randomized, 2-arm, parallel trial will be conducted to examine the effect of pecans on markers of peripheral vascular health, lipids and lipoproteins, blood pressure, and glycemic control.
Phase:
Phase 2
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Penn State University
Collaborator:
American Pecan Council
Criteria
Inclusion Criteria:

- BMI 25-40 kg/m2

- ≥ 1 criterion for metabolic syndrome (i.e., waist circumference ≥ 94 cm men or ≥ 80 cm
women; triglycerides ≥150 mg/dL; HDL-cholesterol ≤ 40 mg/dL men or ≤ 50 mg/dL women;
systolic blood pressure ≥130 mmHg or diastolic blood pressure ≥85 mmHg; fasting plasma
glucose ≥100 mg/dL) at screening

Exclusion Criteria:

- Current use of tobacco-containing products or (≤6 months) cessation

- Allergy/sensitivity/intolerance/dislike of study foods

- Women who are pregnant, lactating, planning to become pregnant or have given birth in
the past year

- Individuals who have had a cardiovascular event (heart attack, revascularization,
stroke), or have a history of heart failure, liver, kidney, autoimmune diseases or
inflammatory conditions such as gastrointestinal disorders or rheumatoid arthritis.

- Type 1 or type 2 diabetes

- Unstable weight ≥10% body weight for 6 months prior to enrollment

- Systolic Blood pressure >160 mmHg for systolic pressure and/or diastolic blood
pressure >/100 mmHg for diastolic pressure at screening

- Fasting blood glucose ≥126 mg/dL at screening

- Triglycerides ≥350 mg/dL at screening

- Taking any medications known to affect lipids, blood pressure, or blood glucose levels

- Diagnosed inflammatory conditions or taking prescribed , taking any chronic
anti-inflammatory medications (>1 time per week over the past 3 months)

- Use of antibiotics within the prior 8 weeks

- Taking supplements (e.g., psyllium, fish oil, soy lecithin, and phytoestrogens) and
botanicals known to affect study outcomes and not willing to cease for the duration of
the study

- Individuals consuming >14 alcoholic drinks/week, and not willing to avoid alcohol
consumption for 48 hours prior to test visit

- Pre-menopausal women who do not have a regular menstrual cycle of 25-35 days

- PI discretion