Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT05897619

Feasibility and Acceptability of a Novel Cognitive Behavioral Skills Mobile App for Pregnant and Postpartum Individuals

Led by Weill Medical College of Cornell University · Updated on 2026-02-27

75

Participants Needed

1

Research Sites

175 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to assess the feasibility and acceptability of the Maya Perinatal Cognitive Behavioral Skills App, a novel app for pregnant and postpartum individuals experiencing difficulties with mood, anxiety, or stress. Participants will complete the 12-module app to learn evidence-based strategies previously shown to help manage mood and anxiety. Assessments will include app feedback questionnaires, feedback interviews, a daily symptom tracker, and symptom measures. The study investigators hypothesizes that participants will find content to be helpful in developing skills to manage anxiety and mood difficulties during the perinatal period, and that the app interface, session structure, and pacing will be acceptable and feasible for this population. It is further hypothesized that increased Maya Perinatal Cognitive Behavioral Skills App use, engagement, and satisfaction will be associated with lower self-reported anxiety and mood symptoms.

CONDITIONS

Official Title

Feasibility and Acceptability of a Novel Cognitive Behavioral Skills Mobile App for Pregnant and Postpartum Individuals

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female, Trans-male, non-binary, gender expansive, or gender questioning gestational carriers of pregnancy
  • Currently pregnant or up to 12 months postpartum
  • 18 years or older
  • Proficient in English
  • Have access to a smartphone or mobile device capable of receiving SMS messages and completing surveys and app modules
  • Available to speak by phone or secure video-conference during the study
Not Eligible

You will not qualify if you...

  • Safety concerns at enrollment, including any suicidal or self-harm thoughts or behaviors within one year
  • Current substance use disorder
  • History of bipolar or psychotic disorder, or current symptoms of psychosis or mania

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Weill Cornell Medical College

New York, New York, United States, 10065

Actively Recruiting

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Research Team

A

Andrea Temkin-Yu, Psy.D.

CONTACT

G

Gail Harrison, MA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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