Anxiety Clinical Trial - Evaluation of Parturients With Anxiety

Status Withdrawn

Clinical Trial Summary

The primary objective of this study is to examine the effects of cognitive bias modification for interpretation (CBM-I) on prenatal anxiety in parturients. Half of the participants will receive CBM-I assignments, while the other half will receive placebo assignments.

Clinical Trial Description

Maternal prenatal anxiety has been shown to have implications on neonatal behavior and early childhood behavioral and emotional wellbeing. Recent studies found that adults using computer-assisted feedback-learning paradigms, referred to as Cognitive Bias Modification for Interpretation (CBM-I), experienced significant reductions in levels of social anxiety, trait anxiety, and depression. Our goal is to identify patients with prenatal anxiety and evaluate the effects of CBM-I on symptoms of prenatal anxiety and patient satisfaction with the labor and delivery experience. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04662463
Study type	Interventional
Source	Harvard Medical School (HMS and HSDM)
Contact
Status	Withdrawn
Phase	N/A
Start date	September 2024
Completion date	December 2026

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