Actively Recruiting

Age: 18Years - 65Years
All Genders
Healthy Volunteers
ID07247487

Comparative Analysis of Diet and Cardiometabolic Health in Adults Following Vegan, Vegetarian, and Omnivorous Diets in Rosario

Led by Universidad del Centro Educativo Latinoamericano · Updated on 2025-12-03

105

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

Sponsors

U

Universidad del Centro Educativo Latinoamericano

Lead Sponsor

U

Universidad Nacional de Rosario

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating how different dietary patterns relate to cardiometabolic health in adults living in Rosario, Argentina. This observational study compares adults following vegan, vegetarian, and omnivorous diets. It aims to understand differences in diet characteristics and cardiometabolic risk profiles, providing insights into potential health benefits and risks tied to each diet type. Participants are grouped into vegan, vegetarian, or omnivorous categories based on their reported consumption of meat, dairy, and eggs. The study collects extensive data, including demographic, medical, dietary, and biochemical information. Diet is recorded over three days and analyzed for nutrient composition. Blood samples are taken after fasting to measure various metabolic and cardiovascular biomarkers. Physical exams include blood pressure, body measurements, and grip strength. During the study, adults complete questionnaires covering physical activity, quality of life, and diet satisfaction. Researchers assess numerous outcome measures such as cholesterol levels, glucose, insulin resistance, inflammatory markers, vitamin and mineral status, body composition, and blood pressure. Data collection occurs from December 2025 to December 2027. The study monitors participants' dietary and health profiles to compare across diet groups and understand cardiometabolic health indicators.

CONDITIONS

Brief Title

Diet and Cardiometabolism in Rosario

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 65 years
  • Residence in the city of Rosario or surrounding areas
  • Without major diseases
  • Body mass index (BMI) greater than 18.5 and less than 30
  • Following a vegan, vegetarian, or omnivorous diet for at least 1 consecutive year at recruitment
Not Eligible

You will not qualify if you...

  • Acute or chronic diseases such as cancer, infections, heart disease, diabetes mellitus, chronic kidney or liver disease, or other conditions affecting study outcomes
  • Gastrointestinal disorders impacting diet
  • Food allergies or intolerances that significantly affect usual diet
  • Pregnant or breastfeeding women
  • High-performance athletes with more than 15 hours per week of high-intensity activity
  • Use of medications affecting study outcomes, including antihypertensives, lipid-lowering drugs, hypoglycemic agents, glucocorticoids, or anti-obesity drugs
  • Problematic use of alcohol or other drugs
  • Participation in another clinical trial
  • Physical or psychological inability to perform required procedures
  • Blood transfusions within the last 3 months (Note: use of vitamins, minerals, or other dietary supplements is allowed)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 2 years

Participants provide demographic, medical, dietary, and biochemical data to evaluate differences among diet groups.

1 initial visit with questionnaires, physical examination, dietary records, and fasting blood sample collection

Long-term Monitoring

Duration - Approximately 2 years (December 2025 to December 2027)

Participants are observed while following their usual vegan, vegetarian, or omnivorous diets with periodic assessments.

Follow-up visits for data collection and health assessments at scheduled intervals

Trial Site Locations

Total: 2 locations

1

Consultorios Prisma

Rosario, Santa Fe Province, Argentina, 2000

Actively Recruiting

2

Universidad del Centro Educativo Latinoamericano

Rosario, Santa Fe Province, Argentina, 2000

Actively Recruiting

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Research Team

A

Ariel Kraselnik, MD

G

Gabriela Giribaldi, RD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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