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Background: Increasing opioid misuse is a worldwide problem. About 10% of opioid misusers are primarily exposed to opioids at the Emergency Department (ED). This study was conducted to determine the feasibility for a clinical trial investigating the effect of Virtual Reality therapy on opioid consumption at the ED.
Methods: Adult patients were included when primarily seen by the Emergency Physician and presenting with a NRS pain score ≥4. Main objective was to identify the target population and evaluate outcome measures to sustain a trial incorporating the Oral Morphine Equivalent (OME) at the ED as the primary endpoint. Primary outcome was mean OME administered at the ED. Secondary outcomes included NRS pain scores, main symptoms and type of analgesics administered at the ED.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patient with NRS pain at rest being 4 or higher | Patient with NRS pain at rest being 4 or higher, primarily treated by emergency physician, internist, or surgeon. All patients receive usual care, no interventions are administered. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Usual care | Other | Patients received usual care |
|
| Measure | Description | Time Frame |
|---|---|---|
| Opioid use | Opioids use of patients during their stay at Emergency Department (yes/no) | throughout study participation, up to 8 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Oral morphine equivalent | Doses of opioids received by a patient during their stay at the ED converted to Oral morphine equivalent (OME) | throughout study participation, up to 8 hours |
| Administered analgesics |
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Inclusion Criteria:
Exclusion Criteria:
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We aim to include all patients ≥16 years, who are admitted to the ED of the Radboudumc and primarily seen by an ED physician.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Radboud university medical center | Nijmegen | Gelderland | 6525 GA | Netherlands |
Data will be made available upon reasonable request.
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| ID | Term |
|---|---|
| D010146 | Pain |
| D059787 | Acute Pain |
| D004630 | Emergencies |
| ID | Term |
|---|---|
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D020969 | Disease Attributes |
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Type and dose of all administered analgesics at Emergency Department.
| throughout study participation, up to 8 hours |
| Pain acceptability | Patient opinion on acceptability of their pain at rest upon admittance and discharge | Asked at moment of admittance and at discharge, up to 6 hours after inclusion |
| Reason why patients finds pain acceptable | Open question | Assessed upon admittance |
| Patients desire for analgesics | yes/no question whether patient desires analgesics | Asked at moment of admittance and at discharge, up to 6 hours after inclusion |
| Patients openness to VR | yes/no question to explore patients willingeness to use VR in their situation | Assessed upon admittance |
| Numaric rating score pain scores at rest | Including whether this is pre/post analgesics | Every 30 minutes until discharge of patient |
| Numaric rating score anxiety scores | NRS anxiety scores | Every 30 minutes until discharge of patient |
| Satisfaction with pain management | On a numaric rating scale | Asked at moment of discharge, up to 6 hours after inclusion |
| Nurse opinion on patient adequacy of pain reporting | Categorical question: understating - adequate - exaggerating | Assessed upon admittance |
| Duration of ED visit | Duration of ED visit | throughout study participation, up to 8 hours |
| Analgesics prescriptions | When patient is discharged home prescribed analgesics are registered. | throughout study participation, up to 8 hours |
| D010335 | Pathologic Processes |