Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
NCT06610552

Powerly - Science-based Digital Intervention Preventing Postpartum Depression and Anxiety

Led by Marta Marciniak · Updated on 2025-05-20

140

Participants Needed

1

Research Sites

143 weeks

Total Duration

On this page

Sponsors

M

Marta Marciniak

Lead Sponsor

U

University of Zurich

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to determine if the Powerly app can help prevent postpartum depression and anxiety in healthy pregnant women. The main questions it aims to answer are: * Does the Powerly app reduce postpartum depression and anxiety? * Does it improve emotion regulation and maternal bonding with a child? Researchers will compare two groups: one using the Powerly app and the other receiving care as usual (CAU) to see if the app leads to better mental health outcomes. Participants will: * Use the Powerly app for four weeks (if in the intervention group). * Complete mental health assessments before the study, after four weeks, and six weeks postpartum.

CONDITIONS

Official Title

Powerly - Science-based Digital Intervention Preventing Postpartum Depression and Anxiety

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Being between 24 and 32 weeks pregnant
  • Owning an iPhone
  • Having sufficient fluency in German language
Not Eligible

You will not qualify if you...

  • Having a high-risk pregnancy
  • Having a history of substance abuse or psychiatric disorders such as bipolar disorder, schizophrenia, or other psychotic disorders
  • Currently using professional face-to-face psychotherapeutic support
  • Participating in other clinical trials or interventions at the same time

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

University of Zurich

Zurich, Switzerland

Actively Recruiting

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Research Team

M

Marta A. Marciniak, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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