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Terminated Not applicable Interventional Results available

[Study Evaluating the Efficacy and Safety of a Digital Therapeutic as an Adjunct to TAU in Postpartum Depression]

ClinicalTrials.gov ID: NCT05551195

Public ClinicalTrials.gov record NCT05551195. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 9:38 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-Blind, Controlled Study Evaluating the Efficacy and Safety of a Digital Therapeutic as an Adjunct to Treatment as Usual Among Women With Mild to Moderate Postpartum Depression

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study evaluates the efficacy of two digital therapeutics, WB001 and ED001, on depressive symptoms among women diagnosed with postpartum depression.

Study identification

NCT ID
NCT05551195
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Woebot Health
Industry
Enrollment
7 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
22 Years to 45 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 16, 2022 (Actual)
Primary completion
May 10, 2023 (Actual)
Completion
May 10, 2023 (Actual)
Last update posted
Feb 24, 2025

2022 – 2023

United States locations

U.S. sites
8
U.S. states
5
U.S. cities
8
Facility City State ZIP Site status
Woebot Investigational Site Lafayette California 94549 —
Woebot Investigational Site Santa Ana California 92704 —
Woebot Investigational Site DeLand Florida 32720 —
Woebot Investigational Site Miami Lakes Florida 33016 —
Woebot Investigational Site Seminole Florida 33777 —
Woebot Investigational Site Decatur Georgia 30033 —
Woebot Investigational Site Glen Oaks New York 11004 —
Woebot Investigational Site Cleveland Ohio 44122 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05551195, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 24, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05551195 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →