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Virtual Reality Biofeedback for Postpartum Anxiety and Depression — VITALISE  

Pregnancy Related Clinical Trial

Official title:
Virtual Reality Biofeedback for Postpartum Anxiety and Depression

Clinical Trial Summary

The purpose of this study is to test patient feasibility and acceptability of virtual reality biofeedback program in postpartum women for anxiety and depression outcomes.

Clinical Trial Description

In an open-label pilot trial, women will undergo a single session using the virtual reality biofeedback program. The objective of this study is to assess feasibility and acceptability of virtual reality biofeedback program in postpartum women with specific assessments of anxiety and depression outcomes. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04925765
Study type Interventional
Source University of Pittsburgh
Contact
Status Completed
Phase N/A
Start date September 1, 2021
Completion date October 15, 2021
View Details
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