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NCT04449341

Can Virtual Reality Reduce Pain and Anxiety During Blood Draw

Completed NA Results posted Last updated 13 July 2021
What this trial tests

NA trial testing Oculus Go headset with Ocean Rift application in Procedural Anxiety in 59 participants. Completed in 9 July 2020.

Timeline
10 June 2020
Primary endpoint
9 July 2020
9 July 2020

Quick facts

Lead sponsorC.R.Darnall Army Medical Center
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposesupportive care
Enrollment59
Start date10 June 2020
Primary completion9 July 2020
Estimated completion9 July 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

C.R.Darnall Army Medical Center

Who can join

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 Pain Primary · 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

GroupValue95% CI
Standard Care Venipuncture With Additional of Virtual Reality6.500.25 – 30.75
Standard Care Venipuncture Without Addition of Virtual Reality5.001.00 – 24.25
Procedural Anxiety Secondary · 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

GroupValue95% CI
Standard Care Venipuncture With Additional of Virtual Reality51.00 – 24.25
Standard Care Venipuncture Without Addition of Virtual Reality6.5.25 – 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.

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Other recruiting trials for Procedural Anxiety

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

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.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing