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N/A Completed N=59 Randomized Single-blind Supportive Care

Can Virtual Reality Reduce Pain and Anxiety During Blood Draw

Procedural Anxiety · Procedural Pain
Source: ClinicalTrials.gov NCT04449341 ↗
Enrolled (actual)
59
Serious AEs
0.0%
Results posted
Jun 2021
Primary outcomePrimary: Procedural Pain — 6.50; 5.00 score on a scale

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.

Outcome Measures

OutcomeResultp-value
PRIMARY
Procedural Pain
6.50; 5.00
SECONDARY
Procedural Anxiety
5; 6.5

Eligibility Criteria

Inclusion Criteria

  • Adults aged 18-50
  • Currently scheduled to undergo venipuncture

Exclusion Criteria

  • Less than 18 years old or greater than 50 years old
  • History of motion sickness (nausea or vertigo)
  • Pregnant women
  • Reported history of blood borne disease (no request will be made for which disease participant has)
  • Use of pain medication(s) on day of study
  • Current use of medical devices, including hearing aids, pacemakers, implanted cardiac defibrillators
  • Currently experiencing headache/migraine
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04449341). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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