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Clinical Trials/NCT05909787
NCT05909787Not yet recruitingNot Applicable

Prevalence of Oral Disorders in Children Identified by Parents in the Context of ENT Pathologies

Assistance Publique - Hôpitaux de Paris0 sites2,000 target enrollmentStarted: July 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
2,000
Primary Endpoint
Difficulty in feeding

Study Overview

Brief Summary

Many children have eating and verbal oral disorders. Our research entitled: PREORA aims to study the prevalence of oral disorders presented in children consulting in ENT department for three months (n = 2000). This first study will be carried out by passing the MCH (Montreal Children's Hospital) feeding scale, a self-questionnaire completed by the parents, in order to assess the presence of disorders according to the parents and will allow us to present oral disorders (Score > 70).

Detailed Description

Over a period of inclusion of 3 months, the doctors of the departement ONT, Robert Debré Hospital, will give written and oral information to the holders of parental authority and to the child at the beginning of the consultation. After a 15-minute reflection period (consultation time), if they agree to participate, parents will answer the doctor's questions and then complete the self-questionnaire.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
1 Day to 17 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients consulting at ENT departement Robert Debré Hospital
  • •Age 0-17 years
  • •Parents and children informed and given their oral consent for the study and speaking french

Exclusion Criteria

  • •Refusal of parents/children to participate

Arms & Interventions

Auto-questionnaire MCH (Montreal Children's Hospital)

Experimental

Auto-questionnaire MCH (Montreal Children's Hospital)

Intervention: Auto-questionnaire (Other)

Outcomes

Primary Outcomes

Difficulty in feeding

Time Frame: 50 minutes

MCH self questionnaire / HME score

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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