CompletedNot Applicable

Textured Food Introduction Information and Parental Feeding Practices

France64 participantsStarted 2016-11-01

Plain-language summary

The purpose of this study is to conduct an intervention with 60 parents of 8 months old children to test the effect of recommendations, compared to usual care, promoting the introduction of textured foods between 8 and 15 months on parental practices of use of textured foods and the effect of such practices on children acceptance for a variety of textured foods.

Who can participate

Age range

1 Month – 7 Months

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * parents ages ≥ 18 years old * children born full term (≥37 weeks) and with weight ≥2500 g * children introduced to complementary feeding after 4 months and before 6 months Exclusion Criteria: * children with episode of tube feedings, chronic disease, allergy and gastroesophageal reflux requiring medication * children introduced to complementary feeding with baby-led weaning method * children already involved in another study on eating behaviour

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Food texture exposure score

Timeframe: End of intervention (15 months)

Textured food acceptance: scale

Timeframe: Pre and post intervention (8 and 15 months)

Trial details

NCT IDNCT04570059

SponsorInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2017-07-13

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