Group therapy shows promise for easing postpartum depression and anxiety
NCT ID NCT06042166
First seen Jun 27, 2026 · Last updated Jul 23, 2026 · Updated 2 times
Summary
This study tested whether a 12-session parenting group therapy, called the Connecting and Reflecting Experience (CARE) program, is helpful and doable for new parents struggling with postpartum depression or anxiety. Seventeen parents of babies aged 3 to 12 months took part. The goal was to see if the program could improve mental health, reduce parenting stress, and strengthen the bond with their baby.
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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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17 people
The number who actually took part.
- Started
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Aug 2024
- Finished
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Nov 2025
- 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 70 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Birthing parent (of any gender) of an infant age 3-12 months old at time of enrollment * Receiving postpartum OB/GYN or mental health services at Montefiore Medical Center * Experienced or currently experiencing moderate to high levels of depression and/or anxiety symptoms in the postpartum period * English-speaking Exclusion Criteria: * Prior participation in a Connecting and Reflecting Experience (CARE) group at any time * Participation in another parenting-focused group during the current postpartum period * Current episode of psychosis or mania or active suicidal ideation * Serious psychiatric, neurocognitive, or substance use related difficulties necessitating a higher level of care than outpatient support (e.g., current inpatient treatment) or that, in the judgment of the PI, would impede group participation (e.g., severe cognitive impairment)
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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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Montefiore Medical Center
The Bronx, New York, 10470, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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