Study of the Parent's Subjective Experience of Parent-child Psychotherapy. (ESPPRI)

December 20, 2022 updated by: Centre Hospitalier Universitaire de Besancon

Study of the Parent's Subjective Experience Following a Parent-child Psychotherapy by Interactive Guidance or Integrative Psychodynamic Psychotherapy.

The child psychiatric care of children under age of 5 years involves taking care of the child, the parent and their interaction. The investigators know that the parent-child relationship plays a key role in attachment and the mental and cerebral development of the child and many studies have shown that the interaction based psychotherapy allows an improvement in the symptoms of the child. The aim of this qualitative and exploratory study is to evaluate the parent's subjective experience of the parent-child psychotherapeutic treatment, i.e., evaluate their experience of the psychotherapy, their relationship with the therapist and a possible change occurring during the psychotherapy. The analysis will be based on semi-structured interviews that will be carried out with the parents.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Detailed Description

Parent-child psychotherapy is the first-line treatment in the context of a dysfunctional parent-child interaction and takes into account both the parent's skills/fragilities, the child's modes of expression of suffering, and their relational modalities.

The care of the parent-child interaction has been the subject of many studies, but has rarely been evaluated from the point of view of the parent, even if the latter is one of the main actors in this interaction.

In France, about 50% of the parent-child psychotherapeutic treatments lead to clinical improvement. They are mainly based on the use of integrative psychodynamic psychotherapies (PPI). PPIs, based on speech, allow the therapist to identify conflicts or anxieties related to the past or present history of the parents and to relate the current troubles of the child to these conflicts of the past. This requires sufficiently significant capacities of narration and mentalization (which consists in the capacity to intellectualize one's own psychic conflicts). The literature shows that for 50% of the population, this treatment does not seem to allow engagement in care. It is important to also explore the relationship between therapist and subject, central element in psychotherapies, and the notion of therapeutic alliance from the subject's point of view. This study aims to evaluate the subjective experience of the parents, following parent-child psychotherapy. The investigaotors consider that the parents are experts in their experience and that the interviews can help them better understand the therapeutic process of the parent-child psychotherapies.

Study Type

Observational

Enrollment (Anticipated)

20

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Parents who have benefited from psychotherapy treatment

Description

Inclusion Criteria:

  • Parent having carried out and completed parent-child psychotherapy with a child in the CHU Minjoz (child under 5 years old)
  • Fluent in French.
  • Not having expressed his opposition to participate.
  • Affiliation to a French social security scheme or beneficiary of such affiliation.

Exclusion Criteria:

  • Parent suffering from a severe and untreated psychiatric illness.
  • Parent and/or dyad benefiting from psychiatric care in a day hospital and/or in full hospitalization
  • Parent whose child has autism or neurodevelopmental disorders.
  • Legal incapacity or limited legal capacity
  • Subject unlikely to cooperate in the study and/or low cooperation anticipated by the investigator
  • Subject without health insurance
  • Pregnant woman
  • Subject being in the period of exclusion from another study or declared in the "national volunteer file".

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Only
  • Time Perspectives: Retrospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Parents
Parent having carried out and completed parent-child psychotherapy with a child in CHU Minjoz (child under 5 years old).
semi-directive interview

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
perception of change
Time Frame: 6 months
Evaluate perception of change using a semi-structured interviews
6 months
Different ability to mentalize and understand the difficulties that had led to a request for psychotherapy
Time Frame: 6 months
Evaluate ability to mentalize and understand the difficulties that had led to a request for psychotherapy using a semi-structured interviews
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Monika Szymanska, PhD, Centre Hospitalier Universitaire de Besançon
  • Study Chair: Livia Vicentini, Centre Hospitalier Universitaire de Besançon
  • Study Chair: Aline Chassagne, PhD, Centre Hospitalier Universitaire de Besançon

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

January 1, 2023

Primary Completion (Anticipated)

September 1, 2023

Study Completion (Anticipated)

December 1, 2023

Study Registration Dates

First Submitted

December 9, 2022

First Submitted That Met QC Criteria

December 20, 2022

First Posted (Estimate)

December 29, 2022

Study Record Updates

Last Update Posted (Estimate)

December 29, 2022

Last Update Submitted That Met QC Criteria

December 20, 2022

Last Verified

December 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 2022/731

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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