App-based cognitive behavioral therapy for preventing postpartum depression
Official title: Examining the Feasibility and Acceptability of a Novel App-based Cognitive Behavioral Therapy Intervention for Preventing Postpartum Depression
Run by Women and Infants Hospital of Rhode Island · NCT06365645 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study is testing a smartphone app that offers support to help prevent postpartum depression in mothers who are at higher risk.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 60 Years |
| Sex | Women only |
| Enrollment | 90 (estimated) |
| Sponsor | Women and Infants Hospital of Rhode Island Academic / other |
| Locations | 1 site (Providence, Rhode Island) |
| Trial ID | NCT06365645 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are English- or Spanish-speaking mothers over 18 years old, who own a smartphone and are receiving prenatal care at the designated clinic.
✕Probably not a fit
Patients with a recent history of depression, anxiety, or other psychiatric conditions, as well as those endorsing active suicidality, will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the feasibility and acceptability of a smartphone application called M.Bapp, which is based on the Mothers & Babies Program, designed to prevent postpartum depression (PPD) among high-risk mothers. The app aims to provide cognitive behavioral therapy (CBT) interventions to women receiving prenatal care, particularly those who may face barriers to traditional in-person therapy. By utilizing evidence-based qualitative research and user-centered design, the study seeks to adapt this effective program into a digital format that can be accessed conveniently by mothers. The goal is to assess how well this app can be integrated into the care of perinatal patients and its potential impact on mental health outcomes.
Why it matters
Potential benefit: If successful, this app could significantly reduce the incidence of postpartum depression among high-risk mothers, improving both maternal and child health outcomes.
How similar studies have gone: Other studies have shown success with app-based interventions for mental health, but this specific adaptation for postpartum depression is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * English- or Spanish-speaking * maternal age \>18 years old * smartphone ownership * receiving prenatal care from a resident or nurse-practitioner/midwifery clinic at the Obstetric and Gynecologic Care Center at WIH * plan to receive postpartum care at the OGCC, * gestational age ≥32 weeks'. Exclusion Criteria: * Active diagnosis or history within five years of depression, anxiety, or other psychiatric condition, as documented in the electronic medical record * Endorsing active suicidality on intake survey or screening positive on EPDS (≥10) or Patient Health Questionnaire (PHQ)-9 (≥10) or GAD-7 (≥8) * prisoners * inability to consent.
Where it's running
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Women & Infants Hospital of Rhode Island
Providence, Rhode Island, United States Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.