MedTrace Logo

Virtual Reality Biofeedback for Postpartum Anxiety and Depression

NCT04925765 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 6

Last updated 2024-04-17

Study results available
· View outcomes & findings →

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.

Conditions

Interventions

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.

Sponsors & Collaborators

  • Grace Lim, MD, MS

    lead OTHER

Principal Investigators

  • Grace Lim, MD,MS · University of Pittsburgh

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2021-09-30
Completion
2021-10-15

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04925765 on ClinicalTrials.gov