CClinicalTrials.gg
Not yet recruitingNCT06184906PEMEDUpdated May 8, 2024

Preventing Celiac Disease by Weaning With Mediterranean Diet

A Phase 3 interventional study of Weaning by Mediterranean Diet in Weaning Failure, sponsored by University of Naples. Not yet recruiting. Open to participants aged 1 Month to 10 Months. Per ClinicalTrials.gov, last updated 2024-05-08.

Sponsored by University of Naples · Phase 3, Interventional, and Prevention

Phase
Phase 3
Study type
Interventional
Enrollment
3,200
Allocation
Randomized
Ages
1 Month to 10 Months
Sex
All
01

Study summary

Background: The introduction of solid foods in alignment with the Mediterranean Diet (MD) post-exclusive milk feeding has been demonstrated to cultivate a lasting affinity for healthy eating during infancy and childhood. Despite this, access to healthy diets remains a challenge for numerous children, particularly in underserved areas. The clinical trial under discussion is set in Scampia, a municipality in Naples, Italy, known for its dense population and socio-economic challenges. This trial, utilizing the Family Pediatrician (FP) system, aims to promote MD nutrition among children in Scampia to potentially prevent or reduce chronic childhood diseases.

Study Design: In this pragmatic trial, FPs are utilized as the unit for randomization to administer the intervention. The intervention group will be introduced to an intensified MD-based diet from weaning, incorporating adult-type MD foods, while the control group will follow standard regional dietary guidelines. Dietary adherence and health outcomes are to be periodically monitored, and genetic and microbiome analyses will be conducted using collected saliva and stool samples. Incorporating a Bayesian group sequential design, this trial is structured to conduct interim analyses for efficacy, aligning with local healthcare systems for optimal resource allocation.

Conclusion: The study is poised to be methodologically innovative and socially impactful, utilizing existing healthcare frameworks to enhance childhood nutrition in challenging environments. Outcomes from this trial are expected to provide valuable insights into the effects of MD-based nutrition on child health and potentially serve as a model for promoting healthier diets in urban suburbs globally.

Read the detailed description

Detailed Description:

The relationship between systemic chronic inflammation and various chronic diseases, such as obesity, diabetes, cancer, autoimmune, and inflammatory bowel diseases, is well-recognized. Given the economic impact of these diseases on healthcare systems, a comprehensive strategy for risk prevention is imperative. Diet and intestinal dysbiosis are identified as major triggers for systemic chronic inflammation. The MD, characterized by its anti-inflammatory qualities, has also been noted for its positive effects on gut microbiota. The timing of introducing the MD is critical for fostering a healthy microbiota, with early exposure being advantageous. Furthermore, early dietary experiences are crucial in shaping future food preferences. Evidence suggests that responsive feeding practices, such as baby-led weaning, may offer protection against obesity. While the early introduction of the MD in children remains under-researched, its potential protective role against diseases like celiac and inflammatory bowel diseases has been suggested. The PEMED trial, designed to promote MD nutrition among children in Scampia, represents a groundbreaking approach, utilizing a Bayesian cluster randomized clinical trial and the Italian family pediatrician system.

This study is unique in its exploration of introducing natural MD foods during infancy and assessing their impact on the establishment of lasting dietary preferences. It leverages the healthcare infrastructure of the Piscinola-Scampia district in Naples for a population-based Pragmatic Clinical Trial, exceeding traditional research design norms. The study is focused on assessing the impact of the MD on the incidence of diseases, employing a Bayesian adaptive sequential approach to allow for ongoing data analysis and adjustments. The PEMED trial's novel approach, combining the early introduction of the MD, population-based surveillance, and an advanced statistical methodology, is poised to set new benchmarks in pediatric research concerning diet and disease prevention.

The trial's objectives include evaluating the impact of the MD on the incidence of pediatric diseases, assessing the development of a 'protective' fecal microbiome, and analyzing the persistence of MD dietary choices in children up to the age of 5 years.

02

Conditions studied

  • Weaning Failure

Browse trials for

Keywords

  • Infant Weaning
  • Mediterranean Diet
  • Celiac Disease
03

In context

Celiac Disease

333 studies on the registry are indexed under Celiac Disease; 77 are open to participants now.

This study's planned enrollment of 3,200 is above the median of 50 across 203 interventional studies indexed under Celiac Disease.

Browse Celiac Disease studies →

Lead sponsor

University of Naples is the lead sponsor of 11 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Month to 10 Months
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

    • Healthy newborns with a birth weight greater than 2000 grams.
  • Residence in Municipality 8, Piscinola-Scampia.

Exclusion criteria

Exclusion Criteria:

    • Newborns suffering from severe prematurity.
  • Newborns with congenital malformations.
  • Newborns afflicted by severe diseases.
05

Study design

Phase
Phase 3
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
3,200 participants (estimated)

Study arms

  • Placebo comparator
    CONTROLS

    Participants in the control arm will undergo a traditional weaning process. This involves primarily the use of industrial baby foods, with a gradual introduction of fresh foods. Legumes will be introduced at around 7-8 months, and fresh fish will be incorporated into the diet after one year of age.

    Dietary Supplement: Weaning by Mediterranean Diet

  • Experimental
    Treated

    Participants in the experimental arm will follow a Mediterranean Diet (MD) weaning schema. This approach includes exclusively fresh foods that are part of the traditional MD, modified to suit infants. Key elements of this diet include: * Seasonal fruit and vegetables, such as broccoli and cauliflower, served as purees from the beginning of weaning. * A variety of fresh blue fish (e.g., anchovies, mackerel, flag fish, cod, sole) introduced at 7 months, seasoned with garlic and cherry tomatoes. * Use of spices and herbs like thyme, marjoram, rosemary, parsley, garlic, and onion to flavor meals. * Exclusion of salt; meals are instead enhanced with 2 g of Parmesan cheese for taste. * Avoidance of sweets.

    Dietary Supplement: Weaning by Mediterranean Diet

Interventions

  • Dietary supplementWeaning by Mediterranean Diet

    Introduce solid foods typical of the Mediterranean Diet at weaning of infants

06

What researchers measure

Primary outcomes

  1. Incidence of Celiac Disease

    Monitoring the incidence of Celiac Disease in the study population.

    Time frame: 3 to 6 years of age

  2. Children growth

    Calculating the Body Mass Index (BMI kg/m\^2) as a measure of growth, assessing if children's BMI falls within the normal range for their age and sex.

    Time frame: 4 to 6 years

Secondary outcomes

  1. Beneficial Microbiome

    Evaluating the composition of the microbiome for beneficial characteristics.

    Time frame: 5 to 6 years of age

  2. Bifidibacteriaceae in the feces

    Measuring the variation of Bifidobacteria in feces.

    Time frame: 5 years

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 8, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06184906
Lead sponsor
University of Naples
Responsible party
Luigi Greco (Professor of Pediatrics, University of Naples) — Principal investigator
First posted
Dec 29, 2023
Start date
Jun 15, 2024 (estimated)
Primary completion
Sep 30, 2030 (estimated)
Completion
Dec 31, 2030 (estimated)
Last update
May 8, 2024

Study contacts

LUIGI GRECO
Contact
ydongre@unina.it
3341587925
RENATA AURICCHIO
Contact
rRenata Auricchio <r.auricchio@unina.it>
+393392507648

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion