NCT04925765

Virtual Reality Biofeedback for Postpartum Anxiety and Depression

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 6 (actual)
• Sponsor: Grace Lim, MD, MS · Academic / Other
• Sex: Female
• Age: 18 Years
• Healthy volunteers: Accepted

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.

Detailed 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.

Conditions

• Anxiety and Depression
• Postpartum Depression
• Pregnancy Related

Interventions

Type	Name	Description
OTHER	Virtual Reality Biofeedback Session	The "Flowly" intervention treatment utilizes virtual reality and biofeedback to train patients to auto-regulate themselves and improve their pain/anxiety/depression.

Timeline

• Start date: 2021-09-01
• Primary completion: 2021-09-30
• Completion: 2021-10-15
• First posted: 2021-06-14
• Last updated: 2024-04-17
• Results posted: 2024-04-17

Locations

1 site across 1 country: United States