Adults 18 to 50, any sex, with Procedural Anxiety or Procedural Pain. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Procedural PainPrimary· 2 months
Determine if use of Oculus Go headset reduces procedural pain perception utilizing the visual analog scale, which measures pain on a linear scale from 0 to 100 millimeters, with 0 being no pain and 100 being maximum pain
Group
Value
95% CI
Standard Care Venipuncture With Additional of Virtual Reality
6.50
0.25 – 30.75
Standard Care Venipuncture Without Addition of Virtual Reality
5.00
1.00 – 24.25
Procedural AnxietySecondary· 2 months
Determine if use of Oculus Go headset reduces procedural anxiety utilizing the visual analog scale, which measures anxiety on a linear scale from 0 to 100 millimeters, with 0 being no anxiety and 100 being maximum anxiety
Group
Value
95% CI
Standard Care Venipuncture With Additional of Virtual Reality
5
1.00 – 24.25
Standard Care Venipuncture Without Addition of Virtual Reality
6.5
.25 – 30.75
Sponsor's own description
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.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by C.R.Darnall Army Medical Center
Last refreshed: 13 July 2021
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04449341.