Assesment of the Efficacy of Personalized Parent-child Psychotherapy in Children Under 3 Years Old

NCT05206708 · tracked via the Priya Life Science France tracker

Sponsor

Centre Hospitalier Universitaire de Besancon

Phase

Not applicable

Started

2022-02-28

Last updated

2024-09-19

Condition(s) studied

Child Behavior DisordersParent-Child Relations

Investigational drug(s) / intervention(s)

Personalized psychotherapyStandard of care

Personalized psychotherapy: Strategy including personalized psychotherapy

Standard of care: Strategy based standard intregrative psychodynamic therapy

Study summary

This study aims to assess the efficacy at 4 months of a personalized strategy comparatively to a standard Psychodynamic Integrative Therapy, on childrens' symptom improvment

Eligibility

Sex

ALL

Min age

—

Max age

3 Years

Healthy volunteers

Inclusion Criteria: * Families who are requesting a consultation for functional or behavioural problems of their child * Children under the age of 3 Exclusion Criteria: * Parents suffering from a severe untreated psychiatric disorder * Difficulties in speaking French * Children with Autistic spectrum disorder * Families already in care

Primary outcome measure(s)

Efficacy of therapy — Month 4
To assess the efficacy at 4 months of a personalized strategy by Interactive Guidance or Psychodynamic Therapy, comparatively to a standard Psychodynamic Therapy, on child symptoms assessed with the "Symptom Check List"

Trial sites (4)

Facility	City	Region	Status
CHU de Besançon	Besançon	France	Recruiting
CHU de Montpellier	Montpellier	France	Not Yet Recruiting
GHU Paris Psychiatrie et Neurosciences	Paris	France	Not Yet Recruiting
CHU de Reims	Reims	France	Not Yet Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05206708 on ClinicalTrials.gov ↗ ← All trials in France