W-PPMA for Postpartum Mothers

Stopped early · Not applicable

Conditions studied: Postpartum Period

In brief

To evaluate the feasibility and acceptability of W-PPMA among a diverse group of postpartum mothers.

Key facts

Study ID

NCT05662605

Run by

Woebot Health

People needed

281

Starts

2023-02-22

Expected to finish

2024-03-17

Last updated by the study team

2024-04-18

Who can join

Age: 16 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• ≥ 16 years of age
• Be ≤ 3 month postpartum
• Currently enrolled in Scripps Research PowerMom study
• Own or have regular access to a smartphone (Android or iOS smartphone with a recent, supported operating system), that can receive SMS messages, and has reliable Wi-Fi access or sufficient data to engage with assigned treatment condition for the duration of the study
• Available and committed to engage with the program and complete assessments for a 16-week duration.
• Ability to read and understand English

You may not qualify if…

• Lifetime diagnosis of a psychotic disorder (including schizophrenia or schizoaffective disorder)
• Lifetime diagnosis of bipolar disorder
• Current suicidal ideation with a plan or intent or a suicidal attempt within the past 12 months
• History of (a) drug and/or alcohol abuse within the past 12 months
• Fetal demise within the past 18 months
• Previous use of the Woebot app

Where it is running

• Scripps Translational Science Institute — La Jolla, California, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.