Assessment of the "Appui Parental": A Program of Early Support to Parenthood

Sponsor
University Hospital, Montpellier (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT02895126
Collaborator
(none)
88
1
2
108.9
0.8

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: "Appui Parental" program
  • Behavioral: Regular parental support
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
88 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Assessment of the "Appui Parental": A Program of Early Support to Parenthood
Actual Study Start Date :
Apr 4, 2014
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
May 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: "Appui Parental" program (44 cases)

Behavioral: "Appui Parental" program

Other: Regular parental support (44 cases)

Usual intervention

Behavioral: Regular parental support

Outcome Measures

Primary Outcome Measures

  1. Symptom Check-List (SCL) score variation [up to 18 months]

Secondary Outcome Measures

  1. Child Behavior Check-List (CBCL) score variation [up to 18 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Month to 20 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Montpellier France

Sponsors and Collaborators

  • University Hospital, Montpellier

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Montpellier
ClinicalTrials.gov Identifier:
NCT02895126
Other Study ID Numbers:
  • 9237
First Posted:
Sep 9, 2016
Last Update Posted:
May 10, 2021
Last Verified:
May 1, 2021
Keywords provided by University Hospital, Montpellier

Study Results

No Results Posted as of May 10, 2021