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Early Intervention to Protect the Mother-Child Relationship After Postpartum Depression (HUGS)

Primary Purpose

Post Partum Depression

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
HUGS
Playtime
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Post Partum Depression focused on measuring Mother-baby interaction, Group therapy, Cognitive behavioral therapy, mother-infant relationship

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion criteria regarding the mother:

  • Person affiliated or beneficiary of a social security plan;
  • Free, informed and written consent signed by the participant and the investigator (at the latest on the day of inclusion and before any examination required by the research);
  • Woman who gave birth in one of the maternity hospitals participating in the study;
  • Diagnosis of postpartum depression made by the perinatal psychiatry team according to the clinical criteria of the DSM-5;
  • Time to onset of depressive symptoms within the first 12 months after childbirth;
  • Treatment for postpartum depression that started at least 8 weeks ago with improved mood as assessed by the psychiatrist.

Inclusion criteria for the baby:

  • Baby aged less than 1 year at inclusion;
  • Twins will be able to participate in the study and benefit from the interventions;

Non-inclusion criteria concerning the mother:

  • Uncontrolled substance use disorder;
  • Presence of suicidal ideas at inclusion;
  • Manic episode of a bipolar disease
  • Psychiatric pathology decompensated upon inclusion and corresponding to the following list: Schizophrenic disorder, Schizoaffective disorder, Mood disorders with psychotic symptoms;
  • Non French speaker.

Non-inclusion criteria for the baby:

- Baby hospitalized or having sustained medical care upon inclusion in the context of a somatic pathology.

Sites / Locations

  • Bordeaux Public Hospital
  • Havre Public Hospital Maternity
  • Reims Public Hospital Maternity
  • Rouen Public Hospital Maternity
  • Toulouse Child Guidance
  • Toulouse Joseph Ducuing Maternity
  • Toulouse Public Hospital Maternity

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

HUGS therapy

Playtime

Arm Description

A structured group intervention that aims to observe mother's behavior and responses with her baby, promote mother-baby interaction through play, and provide tools for positive interaction. This therapy involves cognitive and behavioral work. Therapists observe the mother-baby duo and share their observations from a perspective of encouragement and support. A playful and non-judgmental interaction is cultivated within the group. The main objective is to change the negative trajectory of mother-child interactions through tools from cognitive-behavioral therapies as well as using knowledge about child development.

The participants assigned to the control group will also be in the presence of two therapists, allowing to reproduce the framework of the HUGS therapy. The difference will be the lack of direct therapeutic intervention from the therapists, but only classic psychoeducational guidance. The mothers are offered a time to play with their baby as well as the opportunity to discuss and share their experiences with other mothers, which is generally seen as supportive by them.

Outcomes

Primary Outcome Measures

Mother-infant interaction
The primary endpoint will be the score of factor 1 ("positive affective commitment of the mother as well as her verbalization skills with her baby") of the mother-baby interaction assessment scale The Parent-Child Early Relational Assessment ( PCERA) between the two study groups : HUGS and Playtime. PCERA factor 1 will be measured by analysis of video footage of each mother-baby duo by two independent blind assessors from allocation groups.The score taken into account will be the consensus score between the two evaluators.

Secondary Outcome Measures

Mothers' stress
Parental Stress Index (PSI-3) measured on both groups. This index is categorised in various items (stressors), each including a Likert style index from 1 to 5. The PSI-3 sums up all the items into a score : a high score representing a high stress for the parent.
Mothers' stress
Parental Stress Index (PSI-3) measured on both groups. This index is categorised in various items (stressors), each including a Likert style index from 1 to 5. The PSI-3 sums up all the items into a score : a high score representing a high stress for the parent.
Mothers' stress
Parental Stress Index (PSI-3) measured on both groups. This index is categorised in various items (stressors), each including a Likert style index from 1 to 5. The PSI-3 sums up all the items into a score : a high score representing a high stress for the parent.

Full Information

First Posted
January 11, 2022
Last Updated
August 22, 2023
Sponsor
University Hospital, Toulouse
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1. Study Identification

Unique Protocol Identification Number
NCT05209789
Brief Title
Early Intervention to Protect the Mother-Child Relationship After Postpartum Depression
Acronym
HUGS
Official Title
HUGS : Early Intervention to Protect the Mother-Child Relationship After Postpartum Depression: A Randomized Comparative Trial of the Cognitive Behavioral Therapy Program
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 2023 (Anticipated)
Primary Completion Date
December 2026 (Anticipated)
Study Completion Date
December 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Postpartum depression (PPD) may impair the mother-infant relationship and lead to both short and long-term suboptimal development of the baby. This study aims to evaluate the effectiveness of a targeted intervention (HUGS: Happiness Understanding Giving and Sharing) for enhancing the mother-infant relationship.
Detailed Description
Post-partum depression (PPD) is the most common psychological pathology following childbirth and affects 12% of women in France. This pathology may impair the mother-infant relationship and lead to suboptimal development of the baby in the short and long-term. The prevalence of early interaction disorders is estimated at 73% among women suffering from PPD. Although treatments for PDD are effective, the mother-infant interaction remains impaired, as well as the short, medium and long-term development of the child. It is therefore essential to develop at a very early stage an intervention specifically targeting the mother-infant interaction, and to integrate this care into the general care given to mothers suffering from PPD. A short cognitive-behavioural therapy intervention focused on improving the quality of the mother-infant relationship (the HUGS program: Happiness, Understanding, Giving and Sharing) has been created and validated by Prof. Jeannette Milgrom's Australian team. The objective of our study is to evaluate the effectiveness of the HUGS programme compared to a Playtime control group using a randomised controlled trial in a population of women suffering from PPD and being cared for in 7 French maternity hospitals (Toulouse UHC, Joseph Ducuing Maternity Ward, Toulouse Child Guidance Centre, Reims UHC, Rouen UHC, Le Havre Hospital Group). The comparison will be made 6 months after intervention initiation using "Factor 1: Mother Positive Affective Involvement and Verbalization" of the PCERA (Parent-Child Early Relational Assessment) mother-child interaction evaluation scale.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Partum Depression
Keywords
Mother-baby interaction, Group therapy, Cognitive behavioral therapy, mother-infant relationship

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Multicenter, interregional, comparative, prospective therapeutic study in 2 parallel groups (1: 1), superiority, randomized, blinded for the evaluation of the primary endpoint.
Masking
Participant
Masking Description
group attribution blinded to evaluators for the evaluation of the primary endpoint via video tapes
Allocation
Randomized
Enrollment
104 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HUGS therapy
Arm Type
Experimental
Arm Description
A structured group intervention that aims to observe mother's behavior and responses with her baby, promote mother-baby interaction through play, and provide tools for positive interaction. This therapy involves cognitive and behavioral work. Therapists observe the mother-baby duo and share their observations from a perspective of encouragement and support. A playful and non-judgmental interaction is cultivated within the group. The main objective is to change the negative trajectory of mother-child interactions through tools from cognitive-behavioral therapies as well as using knowledge about child development.
Arm Title
Playtime
Arm Type
Active Comparator
Arm Description
The participants assigned to the control group will also be in the presence of two therapists, allowing to reproduce the framework of the HUGS therapy. The difference will be the lack of direct therapeutic intervention from the therapists, but only classic psychoeducational guidance. The mothers are offered a time to play with their baby as well as the opportunity to discuss and share their experiences with other mothers, which is generally seen as supportive by them.
Intervention Type
Behavioral
Intervention Name(s)
HUGS
Intervention Description
Group therapy with the participation of two therapist positively encouraging mother-baby interactions in a non-judgmental manner
Intervention Type
Behavioral
Intervention Name(s)
Playtime
Intervention Description
Very little intervention from the therapists
Primary Outcome Measure Information:
Title
Mother-infant interaction
Description
The primary endpoint will be the score of factor 1 ("positive affective commitment of the mother as well as her verbalization skills with her baby") of the mother-baby interaction assessment scale The Parent-Child Early Relational Assessment ( PCERA) between the two study groups : HUGS and Playtime. PCERA factor 1 will be measured by analysis of video footage of each mother-baby duo by two independent blind assessors from allocation groups.The score taken into account will be the consensus score between the two evaluators.
Time Frame
6 months after the end of the intervention
Secondary Outcome Measure Information:
Title
Mothers' stress
Description
Parental Stress Index (PSI-3) measured on both groups. This index is categorised in various items (stressors), each including a Likert style index from 1 to 5. The PSI-3 sums up all the items into a score : a high score representing a high stress for the parent.
Time Frame
Right before the intervention (Baseline)
Title
Mothers' stress
Description
Parental Stress Index (PSI-3) measured on both groups. This index is categorised in various items (stressors), each including a Likert style index from 1 to 5. The PSI-3 sums up all the items into a score : a high score representing a high stress for the parent.
Time Frame
Right at the end of the intervention : 28 days after the start of the study
Title
Mothers' stress
Description
Parental Stress Index (PSI-3) measured on both groups. This index is categorised in various items (stressors), each including a Likert style index from 1 to 5. The PSI-3 sums up all the items into a score : a high score representing a high stress for the parent.
Time Frame
6 months after the end of the intervention
Other Pre-specified Outcome Measures:
Title
Socio-economic analysis
Description
the efficiency of the HUGS program compared to usual care, by means of a cost-utility analysis: Costs of support from the point of view of the community and QALYs in order to calculate a differential cost-utility ratio (collected using the EUROQOL EQ-5D-5L scale).
Time Frame
6 months after the end of the intervention

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Mothers
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria regarding the mother: Person affiliated or beneficiary of a social security plan; Free, informed and written consent signed by the participant and the investigator (at the latest on the day of inclusion and before any examination required by the research); Woman who gave birth in one of the maternity hospitals participating in the study; Diagnosis of postpartum depression made by the perinatal psychiatry team according to the clinical criteria of the DSM-5; Time to onset of depressive symptoms within the first 12 months after childbirth; Treatment for postpartum depression that started at least 8 weeks ago with improved mood as assessed by the psychiatrist. Inclusion criteria for the baby: Baby aged less than 1 year at inclusion; Twins will be able to participate in the study and benefit from the interventions; Non-inclusion criteria concerning the mother: Uncontrolled substance use disorder; Presence of suicidal ideas at inclusion; Manic episode of a bipolar disease Psychiatric pathology decompensated upon inclusion and corresponding to the following list: Schizophrenic disorder, Schizoaffective disorder, Mood disorders with psychotic symptoms; Non French speaker. Non-inclusion criteria for the baby: - Baby hospitalized or having sustained medical care upon inclusion in the context of a somatic pathology.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carole GENTILLEAU, MD
Phone
33-5 61 77 13 15
Email
gentilleau.c@chu-toulouse.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Isabelle KIEFFER, CRA
Email
kieffer.i@chu-toulouse.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carole GENTILLEAU, MD
Organizational Affiliation
University Hospital, Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bordeaux Public Hospital
City
Bordeaux
Country
France
Facility Name
Havre Public Hospital Maternity
City
Le Havre
Country
France
Facility Name
Reims Public Hospital Maternity
City
Reims
Country
France
Facility Name
Rouen Public Hospital Maternity
City
Rouen
Country
France
Facility Name
Toulouse Child Guidance
City
Toulouse
Country
France
Facility Name
Toulouse Joseph Ducuing Maternity
City
Toulouse
Country
France
Facility Name
Toulouse Public Hospital Maternity
City
Toulouse
Country
France

12. IPD Sharing Statement

Learn more about this trial

Early Intervention to Protect the Mother-Child Relationship After Postpartum Depression

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