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NCT Number: NCT05206708

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

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

Recruiting

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Key information

Conditions

Child Behavior Disorders Mental Disorders Neurodevelopmental Disorders Parent-Child Relations

Age range

Up to 3 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU de Besançon, Besançon, France

Loading trial locations.

About this study

3 evaluations are performed: before treatment, at the end of the treatment and one year after the treatment.

evaluations include assessment of: children's symptom parent-infant interaction quality parental competencies parental perception of the child by his/her parent parent-therapist alliance hair cortisol concentration

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Personalized psychotherapy

Behavioral

Strategy including personalized psychotherapy

Standard of Care

Behavioral

Strategy based standard intregrative psychodynamic therapy

Other names: Standard intregrative psychodynamic therapy

Primary outcomes

  1. Efficacy of therapy

    Time frame: 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"

Study contacts

Contact information is provided by the study sponsor or research team.

Monika SZYMANSKA, PhD

CONTACT

[email protected]

003381219352

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Besancon

Other

Registry information

Official study title

Assesment of the Efficacy of Personalized Parent-child Psychotherapy Evaluating Symptoms in Children Under 3 Years Old and Parent-child Interaction.

Acronym: ECRIN

Important dates

Study start
2022
Primary completion
2026
Study completion
2026
First posted
Jan 25, 2022
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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