Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT07038681

Mediterranean Diet Intervention for Maternal Postpartum

Led by Universidade do Porto · Updated on 2025-06-26

52

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The increasing prevalence of obesity during women's reproductive years highlights the need for effective strategies to improve nutritional literacy as a preventive approach to adverse postnatal outcomes. This study outlines a protocol for a pilot randomized controlled trial assessing the potential of nutritional education sessions promoting the Mediterranean Diet (MedDiet) to improve adherence to this diet and evaluate its effects on cardiometabolic outcomes, namely on cardiac reverse remodeling, glycemic and blood pressure control, as well as on preconception weight recovery and changes in the fecal microbiota composition in pregnant women with obesity, hypertension, and/or diabetes. Secondarily, this study aims to evaluate how this dietary intervention indirectly interferes with infants' exclusive breastfeeding and the introduction of complementary feeding. It includes a face-to-face session using an eye-catching 13-page manual, followed by five monthly newsletters sent by e-mail. Participants will be monitored at one, six, and twelve months postpartum to evaluate the intervention's effectiveness. Findings from this study will contribute to the development of an evidence-based nutritional education tool designed to improve maternal health outcomes, with potential applicability for both health professionals and pregnant and postpartum women.

CONDITIONS

Official Title

Mediterranean Diet Intervention for Maternal Postpartum

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female aged over 18 years
  • Obesity
  • Chronic arterial hypertension
  • Type 2 diabetes
  • Gestational hypertension
  • Gestational diabetes
Not Eligible

You will not qualify if you...

  • Preexisting cardiomyopathy
  • Renal disease
  • Chronic obstructive airway disease
  • Active systemic infection
  • Genetic syndromes
  • Type 1 diabetes mellitus

AI-Screening

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Trial Site Locations

Total: 1 location

1

Unidade Local de Saúde de São João

Porto, Viana do Castelo District, Portugal, 4200-319

Actively Recruiting

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Research Team

J

Juliana Morais, Master

CONTACT

A

Ana Filipa Ferreira, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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