Can screening and online therapy during pregnancy prevent postpartum depression?
NCT ID NCT07349368
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether screening pregnant women for depression and anxiety and providing tailored online therapy could prevent these conditions after childbirth. Over 3,300 women participated, with some receiving screening and internet-based cognitive behavioral therapy (iCBT) during pregnancy, while others received only standard care. The goal was to see if this approach is effective and practical to roll out on a larger scale.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Stratified internet-based cognitive behavioral therapy (iCBT) with video sessions and telehealth counseling
- What this could lead to
- If successful, this approach could offer a practical, scalable way to reduce postpartum depression and anxiety through early screening and online therapy.
- What could go wrong
- This is a feasibility study, not a large-scale efficacy trial, so results may not be definitive. The intervention relies on smartphone access and self-reporting, which may not work for everyone.
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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3,314 people
The number who actually took part.
- Started
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Mar 2021
- Finished
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Jun 2022
- 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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Accepted
You do not need to have the condition being studied to take part.
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: * The age was ≥18 years old pregnancy and capable of completing the independent assessment of smart phones. Exclusion Criteria: * Exclude those with abnormal comprehension and expression abilities
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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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Jieshou Maternal and Child Health Hospital
Fuyang, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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