Prevalence of Oral Disorders in Children in ENT Pathologies

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

2000 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-07-01

Study Completion Date

2023-11-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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).

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Study of the Prevalence of Pediatric Eating Disorders in Inherited Metabolic Diseases With Dietary Treatment

NCT06471842

Inherited Metabolism Disease

RECRUITING

Impact of Neuropsychological Alteration of Patients With Eating Disorders

NCT04091477

Eating Disorder

COMPLETED

Overview of Knowledge and Practices Among Healthcare Professionals Treating Eating Disorders

NCT07339826

Eating Disorders

RECRUITING

Evaluation of ORALQUEST

NCT04133038

Feeding and Eating Disorders of Childhood

COMPLETED

Evaluation of the Clinical, Neuropsychological and Psychosocial Situation of Patient With Eating Disorders.

NCT02829645

Eating Disorders

UNKNOWN NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Eating Disorders Language Disorders

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Auto-questionnaire MCH (Montreal Children's Hospital)

Group Type EXPERIMENTAL

Auto-questionnaire

Intervention Type OTHER

MCH (Montreal Children's Hospital) self questionnaire completed by the parents

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Auto-questionnaire

MCH (Montreal Children's Hospital) self questionnaire completed by the parents

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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