At a glance
ClinicalIndex Comparison RecordN/ACompleted· 59 enrolled
Drug / intervention
Oculus Go headset with Ocean Rift applicationdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Can Virtual Reality Reduce Patient's Pain, Improve Patient's Experience, and Reduce Procedure Related Anxiety With Venipuncture? A Randomized Control Trial
In Brief
A clinical study evaluating Oculus Go headset with Ocean Rift application for Procedural Anxiety and Procedural Pain. Completed, enrolled 59 participants across 1 site.
Detailed Summary
Adult patients aged 18-50 undergoing blood draw for routine lab evaluation will be randomized to a control group or experimental group to assess if the use of virtual reality reduces procedural pain (primary outcome) and procedural anxiety (secondary outcome) during venipuncture.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsProcedural Anxiety, Procedural Pain
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
202120222023202420252026
Enrollment StartJun 2020
First PostedJun 2020
Primary CompletionJul 2020
TodayJul 2026
First PostedJun 26, 2020
Enrollment StartJun 10, 2020
Primary CompletionJul 9, 2020
TodayJul 2, 2026
Enrollment to primary: 29 daysPosted 6.0 years ago
Interventions
Oculus Go headset with Ocean Rift applicationdevice
Information already included in arm description