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Assessment and Remediation of Oral Disorders (ERTO)

A

Assistance Publique - Hôpitaux de Paris

Status

Not yet enrolling

Conditions

Oral Disorder

Treatments

Other: Psychological care

Study type

Interventional

Funder types

Other

Identifiers

NCT06046768
IDRCB: 2023-A00202-43 (Registry Identifier)
APHP230152

Details and patient eligibility

About

As part of the Reference Center for Rare Diseases of the Robert Debré Hospital, many children have eating and verbal oral disorders. In this doctoral research, we question the psychological impact of oral disorders on the dynamics of family functioning.Our research entitled: Evaluation and Remediation of Orality Disorders (ERTO) aims to evaluate the impact of psychological care of the child and a support program for parents.

We hypothesized that this comprehensive management could contribute to improving disorders and consequently modify parental representations of the child and his disorders.

In addition, care focused on intra-family relations and communication would allow a decentralization and a repositioning of the problem of disorders within the family dynamic.

The results of this research will have concrete applications for the management of children suffering from oral disorders.

Full description

The ERTO search follows the first PREORA search. As soon as the results of the PREORA questionnaires are obtained, we would constitute a cohort of 16 children - a maximum of 32 parents and siblings. It will be extracted from participants in the PREORA study by random draw after screening eligibility according to the inclusion criteria and their desire to participate in this study.

We will study a population of children aged 18 months to 3 years, with ENT pathology, requiring surgery and invasive care.

The research consists of three stages:

T0: An inclusion interview: standardized psychological interview (recorded Stern R interview and PSI Parental Stress Scale). ""R interview"" is a questionnaire published and validated in 1989 by Stern, Robert-Tissot, Besson, et al.

It allows the evaluation of maternal representations. The Parental Stress Index (PSI), translated in Quebec by Bigras and Lafrenière, is used to detect difficulties in parent-child dyads.

T1-T5: Then a follow-up will be proposed (five psychological consultations (interviews, scales), participation in a discussion group for parents in Visio via Zoom, a speech therapy assessment and possible complementary multidisciplinary consultations) T6: Again an assessment with the T0 retest (Stern R Interview, PSI Parental Stress Scale, MCH scale). This study is a non-randomized exploratory research with two controlled groups, before/after.

Parental stress and child representation will be assessed according to the two subgroups of belonging, group A (antenatal diagnosis), group B (postnatal diagnosis), t1 (before psychological management), t2 (after 5 months of psychological management) and t3 (after one year of discussion group). Qualitative and quantitative analyses will be provided, based on variables.

Enrollment

16 estimated patients

Sex

All

Ages

18 months to 3 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Child (boy or girl) with oral feeding disorder(s) diagnosed by a speech therapist as part of a speech therapy assessment
  • Patients under ENT care at Robert Debré Hospital
  • Children aged 18 months to 3 years
  • French-speaking parents
  • Living at home in France
  • Affiliation with a social security scheme or entitled beneficiary
  • Informed consent signed by both parents

Exclusion criteria

  • Pathologies predominantly associated with ENT pathology
  • Neurological disorders
  • Deafness

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

16 participants in 1 patient group

Child with oral feeding disorder(s)
Experimental group
Description:
Child (boy or girl) with oral feeding disorder(s) diagnosed by a speech therapist as part of a speech therapy assessment.
Treatment:
Other: Psychological care

Trial contacts and locations

1

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Central trial contact

Elise CHAUVIN, Doctorant; Natacha TEISSIER, MD PhD

Data sourced from clinicaltrials.gov

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