Reducing Adult Inpatients Anxiety With Virtual Reality Meditation: A Prospective, Randomized Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Anxiety
- Sponsor
- Stanford University
- Enrollment
- 200
- Locations
- 1
- Primary Endpoint
- Hospital Anxiety and Depression Scale (HADS)
- Status
- Not yet recruiting
- Last Updated
- 11 months ago
Overview
Brief Summary
The purpose of the study is to evaluate if non-invasive, distracting devices (virtual reality) can decrease anxiety and improve affect and satisfaction in adult, hospitalized patients.
Investigators
Thomas Caruso
Clinical Professor
Stanford University
Eligibility Criteria
Inclusion Criteria
- •between age 18-99
- •hospitalized at Stanford Health Care
- •english-speaking
Exclusion Criteria
- •significant cognitive impairment or inability to consent
- •current nausea
- •visual problems or currently using corrective glasses that are incompatible with the virtual reality headset
- •a history of severe motion sickness
- •a history of seizures cause by flashing light
- •clinically unstable or require immediate/urgent intervention
Outcomes
Primary Outcomes
Hospital Anxiety and Depression Scale (HADS)
Time Frame: Before and Immediate after intervention
Hospital Anxiety and Depression Scale (HADS) questionnaire. The HADS is a fourteen item scale. Seven of the items relate to anxiety and seven relate to depression. The anxiety and depression subscales each range from 0 to 21, with higher scores indicating higher anxiety/depression complains. Patients were defined as having anxiety or depression or both if the score was 8 or more in the corresponding subscale.