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Whole Food Plant-Based Diet for HIV-Associated Reduction in Cardiovascular Risk (PLANT-HART)

U

Universidad Autonoma de Chihuahua

Status

Completed

Conditions

Hiv
Heart Diseases

Treatments

Behavioral: Nutritional Standard Care
Behavioral: Whole Food Plant-Based Diet Ad Libitum

Study type

Interventional

Funder types

Other

Identifiers

NCT05796882
CI-023 (Other Identifier)
023C-03/23

Details and patient eligibility

About

The goal of this clinical trial is to evaluate the impact of using a whole food plant-based diet in the reduction of cardiovascular risk related to HIV in people who live with HIV infection.

The main questions it aims to answer are:

  • Does a whole food plant-based diet, nonrestrictive in calories and low in fat, reduce the cardiovascular risk associated with HIV infection in people with HIV infection?
  • Does the whole food plant-based diet permit achievement goals in specific metabolic markers of cardiovascular risk (such as Cholesterol, C Reactive Protein)? Participants will follow a non-calorie restricted, low fat, whole food plant-based diet for 8 weeks Researchers will compare standard nutritional care to see if there is a difference in the main outcomes

Full description

The participants in the group within the intervention will follow a Whole Food Plant-Based Diet for 8 weeks, which consists of increasing the daily consumption of fruits and vegetables, including sources of vegetable protein such as legumes (beans, lentils, chickpeas, peas, etc. ), soybeans and their derivatives (tofu, textured soybeans, soymilk), and whole grains (oats, wheat, rice, quinoa, corn), nuts and seeds high in omega-3 fatty acids (chia, flaxseed, hemp ), minimize processed foods and foods high in saturated fat. There will be no caloric restriction, however, visual support will be provided, in the form of a traffic light, to distinguish the frequency with which each type of food can be consumed. A small recipe book will be provided with suggestions for breakfast, lunch, and dinner dishes. Patients will receive vitamin b12 supplements of 1000 micrograms twice a week.

There will be no caloric restriction, however, visual support will be provided, in the form of a traffic light, to distinguish the frequency with which each type of food can be consumed. A small recipe book will be provided with suggestions for breakfast, lunch, and dinner dishes. Patients will receive vitamin b12 supplements of 1000 micrograms twice a week.

The participants in the other group will attend a consultation with a nutritionist every month in which will receive recommendations about nutrition and lifestyle in order to reduce cardiovascular risk.

Enrollment

10 patients

Sex

All

Ages

20 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Over 20 years but under 60 years
  • Individuals with a BMI >25
  • Individuals with some classic cardiovascular risk factor (dyslipidemia, smoking, type 2 diabetes mellitus, systemic arterial hypertension, obesity)
  • Individuals under ART with adequate CD4+ cell count and viral load undetectable

Exclusion criteria

  • Patients currently diagnosed with AIDS
  • Patients who have suffered an AMI and/or stroke
  • Patients who use drugs
  • Patients who have had poor adherence to ART

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

10 participants in 2 patient groups

WFPBD Group
Experimental group
Description:
The participants in this group follow a Whole Food Plant-Based Diet for 8 weeks
Treatment:
Behavioral: Whole Food Plant-Based Diet Ad Libitum
Nutritional Standard Care Group
Active Comparator group
Description:
The participants in this group receive a nutritional consultation every month with dietetic guidance and recommendations about a healthy lifestyle, duration 8 weeks
Treatment:
Behavioral: Nutritional Standard Care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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