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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02895126
Other study ID # 9237
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 4, 2014
Est. completion date October 18, 2022

Study information

Verified date September 2023
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In so-called at risk families, the child-parent attachment relationship is more difficult to set up and this can be a barrier to social and emotional development of young children. To help parents build and sustain this relationship, and to prevent child development disorders, many parenting programs have been created, usually with frequent home visits by early childhood professionals. In France, therapeutic interventions at home are little used and they are not evaluated. In Montpellier, an action of this type has been conducted since 2001 by the "Conseil Départemental de l'Hérault" in collaboration with the University Hospital of Montpellier including, in addition to home visits, supervision of professionals: the Appui Parental Program. Before extending this action to other areas of Herault, the "Conseil Départemental de l'Hérault", the "Abri Languedocien" and the University Hospital of Montpellier are conducting an assessment to know the effectiveness of the program for families under care. This 3-year multicenter prospective study includes 88 children aged 1 to 20 months from families meeting vulnerability criteria previously defined, 44 benefiting Appui Parental program (experimental group) and 44 benefiting a regular support (control group). A paediatric examination on the basis of the Denver scale, parental questionnaires, questionnaires to professionals and an a video of infant-parent interactions are used. The data, collected at baseline and 18 months later, will be compared.


Description:

Objective: the main objective of this study is to determine the efficiency of Appui Parental program by evaluating its impact on the development of children aged from 0 to 3 years. The secondary objectives are to study the effects of the intervention on: the mother-child interactions, the degree of therapeutic alliance between parent and professionals, the parenting skills feeling, perceived social support, anxiety and depression of parents, frequency of legal interventions (placements, educational measures). An assessment of stress among professionals involved in the study and evaluation of the therapeutic alliance with families will also be conducted to assess the effectiveness of the supervision included in the program. Hypothesis: Scores on Symptom Check List after 18 months of follow up will be significantly higher in subjects who benefited the Appui Parental program compared to subjects with conventional parental support. Similarly, it is expected that other developmental assessments of children have the best results in the Appui Parental Program group than in the control group. Finally, it is assumed that the mother-child interactions, the parenting skills feeling, and the therapeutic alliance between parent and professional are better in the Appui Parental program than in the control group.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date October 18, 2022
Est. primary completion date October 18, 2022
Accepts healthy volunteers No
Gender All
Age group 1 Month to 20 Months
Eligibility Inclusion Criteria: - family with child between 1 and 20 months of age and with parents eligible to parental support, - written informed consent signed by both parents or 1 legal guardian, - vulnerability criteria with difficulties to meet the needs of their child, - family affiliated to social security. Exclusion Criteria: - mother having delusional psychosis, - family whose child is in danger and needs an immediate protective measure, - ongoing justice procedure for the child, - family with impossibility to follow-up during 18 months, - non French-speaking parents.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
"Appui Parental" program

Regular parental support


Locations

Country Name City State
France University Hospital Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Symptom Check-List (SCL) score variation up to 18 months
Secondary Child Behavior Check-List (CBCL) score variation up to 18 months
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