Talking therapy eases pregnancy anxiety, study finds
NCT ID NCT04581681
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a 6-week group therapy program (cognitive behaviour therapy) could help reduce anxiety and stress in pregnant women and new mothers. 72 women from Manitoba, Canada, who were pregnant or within 12 months postpartum and had an anxiety disorder took part. The therapy was delivered online and focused on understanding anxiety, self-care, facing fears, bonding with baby, and preventing relapse. The goal was to see if this approach improves mental health for mothers and their babies.
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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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72 people
The number who actually took part.
- Started
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Dec 2020
- Finished
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Jan 2023
- 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 years and older
- 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: * Adult over the age of 18 years living in the province of Manitoba, Canada. * Must be pregnant or within 12 months postpartum. * Women must also meet criteria for at least one anxiety disorder or related disorder (i.e., generalized anxiety disorder, social anxiety disorder, panic disorder with or without agoraphobia, obsessive-compulsive disorder, or posttraumatic stress disorder). Exclusion Criteria: * Primary perinatal depression * Active suicidality and/or homicidality * Active psychosis, manic, or a substance use disorder that would interfere with participation in treatment. * Women also must not be receiving concurrent psychotherapy * If on medication, must not have made any medication changes in the 6 weeks prior to beginning participation in our study.
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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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St. Boniface Hospital
Winnipeg, Manitoba, R2H2A6, Canada
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