HUGS therapy aims to strengthen Mother-Baby bond after postpartum depression
NCT ID NCT05209789
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a group therapy program called HUGS for mothers with postpartum depression. The goal was to see if it improves the mother-baby relationship compared to a playtime group. 104 mothers participated, and researchers measured bonding through video analysis. The therapy focuses on positive interactions and support.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- group therapy (HUGS program)
- What this could lead to
- If it works, this could provide a simple, non-drug way to help mothers with postpartum depression bond better with their babies.
- What could go wrong
- This is a small, completed trial with 104 participants, so results may not apply to all mothers. The therapy is behavioral, so benefits depend on engagement and may not be dramatic.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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104 people
The number who actually took part.
- Started
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Dec 2023
- Finished
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Mar 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 100 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Bordeaux Public Hospital
Bordeaux, France
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Havre Public Hospital Maternity
Le Havre, France
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Reims Public Hospital Maternity
Reims, France
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Rouen Public Hospital Maternity
Rouen, France
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Toulouse Child Guidance
Toulouse, France
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Toulouse Joseph Ducuing Maternity
Toulouse, France
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Toulouse Public Hospital Maternity
Toulouse, France
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