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Can Virtual Reality Reduce Pain and Anxiety During Blood Draw

NCT04449341 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 59

Last updated 2021-07-13

Study results available
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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.

Conditions

  • Procedural Anxiety
  • Procedural Pain

Interventions

DEVICE

Oculus Go headset with Ocean Rift application

Information already included in arm description

Sponsors & Collaborators

  • C.R.Darnall Army Medical Center

    lead FED

Principal Investigators

  • Matthew J Perdue, PA · C.R.Darnall Army Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-06-10
Primary Completion
2020-07-09
Completion
2020-07-09
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04449341 on ClinicalTrials.gov