MedPath

sing Virtual Reality to manage patient anxiety during painful procedures in Emergency Department (VR-ED)

Not Applicable
Conditions
Procedure related anxiety
Public Health - Health service research
Emergency medicine - Other emergency care
Mental Health - Anxiety
Registration Number
ACTRN12623000715673
Lead Sponsor
Metro South Healthcare Service
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

patients will be eligible for inclusion if they are greater than or equal to 18 years old, require needle related painful procedures (including venipuncture/cannulation, wound closure, drainage of abscess or knee joint aspiration), reported moderate or high anxiety level (VAS-A score greater than or equal to 40) and provided informed written consent.

Exclusion Criteria

Patients will be excluded if they requiring urgent care; has a history of blindness, intellectual disability, cognitive impairment, dementia, severe motion sickness, claustrophobia, epilepsy; has nausea/vomiting, vertigo/dizziness, head or facial injury/head or facial wound, respiratory symptoms or in isolation, does not speak English, or has been previous enrolled in the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Feasibility of a full powered trial will be determined based on percentage of eligible participants provided consent (>60%), tolerated the procedure (>70%), withdraw or lost follow up (<5%), adhere to protocol (>80%), participants and staff (nurses and doctors) satisfaction and acceptability (80% scored >=7 on a scale of 10), and effect size estimates. The percentage of eligible participants provided consent, tolerated the procedure, withdraw or lost follow up, adhere to protocol will be assessed via audit of study records. The percentage of participants and staff (nurses and doctors) satisfaction will be assess via 5 point Likert scale. The acceptability will be assessed using the Acceptability of Intervention Measure (AIM). [Upon conclusion of the study. ]
Secondary Outcome Measures
NameTimeMethod
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