N/A
Completed N=6
Virtual Reality Biofeedback for Postpartum Anxiety and Depression
Anxiety and Depression · Depression · Pregnancy Related
Source: ClinicalTrials.gov NCT04925765 ↗
Enrolled (actual)
6
Serious AEs
0.0%
Results posted
Apr 2024
Primary outcomePrimary: Intervention Feasibility — 4.83 score on a scale
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Intervention Feasibility |
4.83 | — |
| PRIMARY Intervention Acceptability |
5 | — |
| SECONDARY Decrease in Depression From Baseline to Post-intervention |
5 | — |
| SECONDARY Decrease in State-Trait Anxiety Inventory (STAI) From Baseline to Post-intervention |
5 | — |
Eligibility Criteria
Inclusion Criteria
- Currently pregnant or postpartum (delivery within 3 months)
- 18 years or older
Exclusion Criteria
- Unable to participate in study procedures
- English illiterate (surveys validated in English)
Data sourced from ClinicalTrials.gov (NCT04925765). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.