- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05157633
Oral Exploration of Objects and Food Diversification (OPENING)
Eating difficulties in infants and young children are defined as all the difficulties in feeding oneself in an appropriate and satisfactory manner. These disorders affect approximately 20 to 25% of infants and young children, and thus constitute one of the most frequent reasons for consultation in these age groups. Many of these children continue to be received in consultation.
Studies show that the lack of intraoral exploration in children could be associated with later difficulties in accepting different textures or new foods. Our clinical examination of sensorimotor functions shows signs of sensory hyper reactivity that are very common in children who always wipe their hands when in contact with food or sticky objects and for those who experience difficulty in brushing or grooming themselves.
In all of the publications available which includes pubmed, there is no mention of the lack of exploration of objects and the stigma of sensory hyper-responsiveness even if this latter was not entirely detailed in the descriptions made.
The trial hypothesis is that this exploration defect corresponds to early sensory hyperreactivity which also plays a deleterious role in the acceptance of new textures and new foods.
In this trial we propose a comparison study with a controlled population of children without eating difficulties as defined by the Montreal MCH score to validate a statistical link between the difficulties in food diversification beyond 18 months and the lack of exploration of the environment with 'mouthing' between 6 and 10 months.
Investigators will analyse consultation questionnaires dedicated to eating difficulties retrospectively (patients) and will compare them with questionnaires of children from daycares without eating difficulties (controls).
Study Overview
Detailed Description
To conduct this study the controls will be recruited from daycares and different nursery schools after agreement with the heads of establishments.
Two questionnaires along with an information note will be distributed to the parents and will be completed in a non-identifying manner, retrieved by the teachers and then sent to the principal investigator.
The questionnaires include the validated Montreal HME questionnaire which will detect the possible existence of eating difficulties and a more general questionnaire on the psychomotor development of the child (not validated because a qualitative questionnaire without a score). The collection of data will be prospective for controls.
Patients on the other hand will be recruited retrospectively from the dedicated oral consultation at the Hospital.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Paris, France, 75019
- CHU Robert Debré, 48 Bd Sérurier
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- For patients: Children aged between 9 months and 6 years with eating difficulties defined by the Montreal HME score> = 61.
For controls: children aged between 9 months and 6 years attending a crèche who agreed to participate in the study.
Not opposing participation in the study.
Exclusion Criteria:
Exclusion of controls who have:
- an eating disorder defined by an MCH score> = 61 (score defined for the inclusion criteria)
- encephalopathy, neuro-metabolic disorder, genetic syndrome (after response to the questionnaire)
For patients and controls:
- Encephalopathies
- Neuro-metabolic disorders
- Suspected or identified genetic syndromes
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Other
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Controls
Children without eating difficulties
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questionnaire food scale: HME data collection of food survey
|
|
Patients
Children with eating difficulties
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of participants with a delay or lack of acquisition of oral exploration of objects.
Time Frame: 1 day
|
Deferred presence or absence of the acquisition of the competence of oral exploration of objects between 6 and 10 months by a qualitative questionnaire without score not validated
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To determine if there is a link between the inability to orally explore objects and difficulties in seeing and/or touching and/or smelling certain types of food
Time Frame: 1 day
|
Number of children with difficulty seeing and / or touching and / or smelling certain types of food and an inability to explore objects orally.
|
1 day
|
|
To determine if there is a link between the inability to orally explore objects and difficulties in seeing and/or touching and/or smelling certain types of food
Time Frame: 1 day
|
Percentage of children with difficulty seeing and / or touching and / or smelling certain types of food and an inability to explore objects orally.
|
1 day
|
|
To determine if there is a link between the inability to orally explore objects and the inability to touch certain non-food textures
Time Frame: 1 day
|
Number of children with an inability to touch certain non-food textures and an inability to orally explore objects by a qualitative questionnaire without score not validated
|
1 day
|
|
To determine if there is a link between a link between the inability to orally explore objects. And the inability to touch certain non-food textures
Time Frame: 1 day
|
percentage of children with an inability to touch certain non-food textures and an inability to orally explore objects
|
1 day
|
|
To determine if there is a link between a link between the inability to orally explore objects and the absence of crawling in motor development.
Time Frame: 1 day
|
Number and percentage of children who have crawled in their psychomotor development
|
1 day
|
|
To determine if there is a link between a link between the inability to orally explore objects and the absence of crawling in motor development.
Time Frame: 1 day
|
Number of children who orally explored the objects
|
1 day
|
|
To determine if there is a link between a link between the inability to orally explore objects and the absence of crawling in motor development.
Time Frame: 1 day
|
percentage of children who orally explored the objects
|
1 day
|
|
To determine if there is a link between an incidence of constipation in both groups of children
Time Frame: 1 day
|
Number of children with constipation according to ROME IV criteria
|
1 day
|
|
To determine if there is a link between an incidence of constipation in both groups of children
Time Frame: 1 day
|
percentage of children with constipation according to ROME IV criteria
|
1 day
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- OPENING
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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