Skip to content

Impact of Virtual Reality on Anxiety in Patients Undergoing Interventional Procedures

Assessing the Impact of Immersive Virtual Reality Experience on Injection-related Anxiety in Patients Undergoing Interventional Pain Spine Procedures: a Prospective Randomized Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05744336
Enrollment
64
Registered
2023-02-27
Start date
2023-03-12
Completion date
2024-11-30
Last updated
2024-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety

Keywords

Anxiety, Pain Procedures, Virtual Reality

Brief summary

Periprocedural anxiety is a common problem for patients who undergo interventional pain procedures. Virtual Reality (VR) is an immersive experience that has gained acceptance in the medical field as a tool for reducing anxiety and pain for patients.Research Aim: To evaluate the effect of immersive virtual reality (VR) on periprocedural anxiety related to therapeutic cervical epidural steroid injections (ESI). The investigators hypothesize that immersive virtual reality will result in a clinically meaningful anxiety reduction, defined as the proportion of participants with \> 50% reduction in Numeric Rating Scale (NRS) anxiety scores when compared to participants in the non-treatment group who will have standard preprocedural waiting time conditions in clinic, but no VR experience. Similarly, the investigators hypothesize a significant reduction in objective sympathetic tone as measured by skin sympathetic nerve activity (SKNA).

Interventions

OTHERGroup 1 Immersive Virtual Reality (VR)

Participants in Group 1 Immersive Virtual Reality (VR) participants wear the device covering their eyes. The viewing experience will include calming nature sounds for between 15-20 minutes before their planned plain clinic procedure

Group 2 control group participants have no preprocedural intervention. Standard clinic waiting conditions for 15-20 minutes before their planned pain clinic procedure.

Sponsors

Northwestern University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Randomized controlled observational trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-80 years old at day of enrollment * Neck pain patient deemed to be a candidate for pain control treatment with interventional fluoroscopically guided cervical epidural steroid injection as determined by their pain medicine provider based on history, physical exam, and radiographic findings * Willingness to undergo pre-procedural intervention of VR viewing experience or equivalent pre-procedural wait time * No history of prior epidural steroid injections * Did not receive sedatives prior to or during procedure

Exclusion criteria

* Refusal / inability to participate or provide consent * Contraindications to injection (anticoagulated states, allergy to components of injection, local infection at injection site, current infectious process or treatment of antibiotics for current infection) * Uncontrolled anxiety disorder or untreated/inadequately treated psychiatric disorder * History of Alzheimer's, dementia, or cognitive dysfunction * Patient currently taking benzodiazepines * Severe motion sickness * Seizure disorder * Vision loss * Non-English speaking patients

Design outcomes

Primary

MeasureTime frameDescription
Numeric rating score for anxiety while positioning on the fluoroscopy table.Before planned procedureNumeric rating score for anxiety on an 11-point scale, ranging from 0 (no anxiety at all) to 10 (worst possible level of anxiety) when positioning on the fluroscopy table.
Numeric rating score for anxiety when local anesthetic is injected.Start of planned procedureNumeric rating score for anxiety on an 11-point scale, ranging from 0 (no anxiety at all) to 10 (worst possible level of anxiety) when local is injected.
Numeric rating score for anxiety when the epidural needle is removed.End of planned procedureNumeric rating score for anxiety on an 11-point scale, ranging from 0 (no anxiety at all) to 10 (worst possible level of anxiety) after the epidural needle is removed

Secondary

MeasureTime frameDescription
Procedural pain during epidural steroid injection reported by participants.During planned procedureNRS Level of subjective procedural pain during epidural steroid injection recorded by numeric rating score on a scale of 0 (no pain) to 10 (worst pain imaginable) Level of subjective procedural pain during epidural steroid injection recorded by NRS
Timepoint at peak of numeric rating score anxiety ratingThrough study completion average of 2 hoursTimepoint at peak numeric rating score for anxiety (NRS) 0 (no anxitey) to 10 (worst anxiety).

Countries

United States

Contacts

Primary ContactPaul Fitzgerald, RN,BSN,MS
p-fitzgerald2@northwestern.edu312-695-1064
Backup ContactJason Ross, MD
jason.ross@nm.org312-695-0061

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026