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Recruiting NCT06839846

NCT06839846 Survey of Different Modes of Weaning in Pediatric Population

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Clinical Trial Summary
NCT ID NCT06839846
Status Recruiting
Phase
Sponsor IRCCS Azienda Ospedaliero-Universitaria di Bologna
Condition Weaning
Study Type OBSERVATIONAL
Enrollment 500 participants
Start Date 2022-04-01
Primary Completion 2025-06-30

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 500 participants in total. It began in 2022-04-01 with a primary completion date of 2025-06-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Infant weaning refers to the transition from a diet based on the exclusive intake of milk (mother's milk or formula) to a diversified diet that is complete with all the nutrients necessary for proper infant development. For this purpose, a diet supplementary to milk, which is gradually reduced, is undertaken in order to gradually acquire the dietary pattern followed by the family. There are different types of weaning, which vary according to traditions, ethnicity and scientific currents. These include traditional weaning and on-demand self-weaning. The former consists of weaning with specific infant foods (example: freeze-dried, homogenized, vegetable broth, creams..) offered at set doses, quantities, and times. On the other hand, 'autodivezzamento on demand is a mode of weaning entrusted to the child's request, leaving the child to choose quantities and types of food, even prepared at home, during family meals. The aim of our study is to establish the prevalence of different modes of weaning and the perception of advantages and disadvantages related to them by parents and Free Choice Pediatricians by means of two different dedicated questionnaires. The study also aims to assess possible risks resulting from the transition to complementary feeding, for example, errors in feeding or inhalation of foreign bodies.

Eligibility Criteria

Inclusion Criteria: Parents group: * Overage parents with children between the ages of 4 and 18 months * Need to have an electronic tool that allows direct access to the link connected to an internet network * Understanding of the Italian language * Obtaining informed consent from the parent completing the questionnaire Pediatricians group: * Activities of Free Choice Pediatrician in Italy. * Need to have an electronic tool that allows direct access to the link connected to an Internet network * Obtaining informed consent Exclusion Criteria: Parents group: \- Parents of children with chronic neurological diseases, dysphagia, chronic diseases involving specific diet, intestinal diseases resulting in malabsorption; Pediatricians group: \- None

Contact & Investigator

Central Contact

Arianna Dondi, MD

✉ arianna.dondi@aosp.bo.it

📞 0512143012

Principal Investigator

Arianna Dondi, MD

PRINCIPAL INVESTIGATOR

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Frequently Asked Questions

Who can join the NCT06839846 clinical trial?

This trial is open to participants of all sexes, studying Weaning. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06839846 currently recruiting?

Yes, NCT06839846 is actively recruiting participants. Contact the research team at arianna.dondi@aosp.bo.it for enrollment information.

Where is the NCT06839846 trial being conducted?

This trial is being conducted at Imola, Italy, Carpi, Italy, Bologna, Italy, Bologna, Italy.

Who is sponsoring the NCT06839846 clinical trial?

NCT06839846 is sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna. The principal investigator is Arianna Dondi, MD at IRCCS Azienda Ospedaliero-Universitaria di Bologna. The trial plans to enroll 500 participants.

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