Skip to content

Functional Yogurt Consumption and Its Effects on the Lipid Profile of Healthy Subjects

Evaluation of the Effect of Consuming Yogurts Fortified With Dietary Sources of Vitamin E and Omega-3 on Classical Biomarkers of Cardiovascular Disease and Blood Levels of Vitamin E.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06574711
Acronym
FYOPO
Enrollment
54
Registered
2024-08-28
Start date
2022-03-22
Completion date
2024-05-07
Last updated
2024-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Apolipoproteins, Cardiovascular Diseases, Food Preferences, Functional Food, HDL, Low-density-lipoprotein-type, Triglycerides

Keywords

PUFA, cardiovascular risk, lipid profile, healthy volunteers, yogurt, sacha inchi oil, interspecific hybrid palm oil

Brief summary

The purpose of this study was to assess the effect of the daily intake of yogurts enhanced with Sacha Inchi oil and hybrid palm tree oil on human plasma lipids related to cardiovascular risk factors

Detailed description

After being recruited and signing a written informed consent about the study and potential risks, the participants were randomized and assigned in a double-blind manner to one of three intervention groups (control yogurt, sacha inchi oil yogurt, or hybrid palm tree oil yogurt; consumption 1 bottle of 200ml per day for 90 days.

Interventions

OTHERSacha inchi oil yogurt

Sacha inchi oil was incorporated into a nonfat yogurt acting as a source of linolenic acid

OTHERHybrid palm oil yogurt

Interspecific hybrid palm oil was incorporated into a nonfat yogurt as a source of bioactive compounds

Conventional full-fat yogurt

Sponsors

Universidad Nacional de Colombia
CollaboratorOTHER
Pontificia Universidad Javeriana
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

Forty-seven subjects were randomized and assigned to one of the three intervention groups supplemented daily with 200g of: Sacha Inchi Oil (SIO)-containing yogurt (Group-A), Hybrid palm oil (HPO)-containing yogurt (Group-B), and plain yogurt (Group-C).

Intervention model description

A pilot randomized; double-blind, parallel-controlled pragmatic trial was performed

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Normal total cholesterol (≤200mg/dl) levels * Have a yogurt consumption habit of at least three times a week * Maximum level of moderate physical activity * Body mass index (BMI) of ≤29.9kg/m2 * Serum triacylglycerols below 400mg/dl

Exclusion criteria

* Presence of chronic disease (Arterial hypertension, Diabetes Mellitus, among others) * A history of illicit drug use and/or chronic alcohol use, active smoking * A well-established allergy to red palm olein and/or milk and its derivatives * Consumption of nutritional supplements (antioxidants, omega 3, fiber, phytosterols) * Pregnancy or lactation * Having menopause * High consumption of nuts, flaxseed, chia, and sesame seeds

Design outcomes

Primary

MeasureTime frameDescription
Change in plasma levels of total cholesterolBaseline, 1 month, 2 months and 3 monthsMeasure in plasma (mmol/l)
Change in plasma levels of LDL-cholesterolBaseline, 1 month, 2 months and 3 monthsMeasure in plasma (mmol/l)
Change in plasma levels of HDL-cholesterolBaseline, 1 month, 2 months and 3 monthsMeasure in plasma (mmol/l)
Change in plasma levels of triacylglycerolsBaseline, 1 month, 2 months and 3 monthsMeasure in plasma (mmol/l)
Change in plasma levels of Apolipoprotein A1 (ApoA1)Baseline, 1 month, 2 months and 3 monthsMeasure in plasma (g/l)
Change in plasma levels of Apolipoprotein B (ApoB)Baseline, 1 month, 2 months and 3 monthsMeasure in plasma (g/l)
ApoB/ApoA1 ratioBaseline, 1 month, 2 months and 3 monthsprognostic predictor of a 10 year cardiovascular event

Countries

Colombia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026