Virtual Reality Pain Study

Last updated: March 23, 2022
Sponsor: Baylor Research Institute
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT05293275
IRB 021-367
  • Ages > 18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

Investigating pain in hospitalized patients in two groups: virtual reality usage group vs standard of care

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • • patients at least 18 years of age,
  • reported pain in last 24 hours ≥ 3 on the Numerical Rating Scales (NRS),
  • patients undergoing surgery,
  • expected hospital length of stay of at least 48 hours,
  • English fluency,
  • willing to comply with study procedures.
  • Hx opioid use

Exclusion

Exclusion Criteria:

  • • gross cognitive impairment that would interfere with the ability to consent orcomplete study procedures
  • current or prior diagnosis of epilepsy, seizure disorder, dementia, or migraines,
  • hypersensitivity to flashing light or motion,
  • history of motion sickness or cyber sickness,
  • medical condition predisposing to or current nausea, vomiting or dizziness,
  • stereoscopic vision or severe hearing impairment,
  • injury to eyes, face or neck that impedes comfortable use of virtual reality,
  • cancer related pain,
  • PHQ-9 screen indicating suicidal ideation, patients will be referred toappropriate clinical intervention (see suicide protocol)
  • currently pregnant,
  • current or recent completion of participation in any interventional pain study (with in past 2 months)
  • substance abuse (alcohol or illegal drugs): Alcohol- NIAAA definition of heavydrinking as more than 4 drinks on any day or more than 14 drinks per week formen, more than 3 drinks on any day or more than 7 drinks per week for women. Anyillegal drugs including marijuana

Study Design

Total Participants: 100
Study Start date:
March 15, 2022
Estimated Completion Date:
October 31, 2023

Study Description

Patients will be randomized to either the virtual reality group or the standard of care group. The virtual reality group will use the device over two days. Both groups will answer questionnaires regarding their pain and anxiety. Medical records will be used to look at pain medication usage in both groups.

Connect with a study center

  • Baylor Institute for Rehabilitation

    Dallas, Texas 75246
    United States

    Active - Recruiting

  • Baylor University Medical Center

    Dallas, Texas 75246
    United States

    Active - Recruiting

  • Baylor Scott and White Hospital-Temple

    Temple, Texas 76508
    United States

    Site Not Available

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