- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05668234
Study of the Parent's Subjective Experience of Parent-child Psychotherapy. (ESPPRI)
Study of the Parent's Subjective Experience Following a Parent-child Psychotherapy by Interactive Guidance or Integrative Psychodynamic Psychotherapy.
Study Overview
Status
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
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Lauriane Vulliez, Pr
- Phone Number: 0033 0381218154
- Email: lvulliez@chu-besancon.fr
Study Contact Backup
- Name: Astrid Pozet
- Phone Number: 0033 0381218988
- Email: apozet@chu-besancon.fr
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
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
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
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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