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Study and evaluate the effectiveness of virtual reality in pain management.
Study and evaluate the effectiveness of virtual reality in pain management.This is an open prospective observational study carried out at Urgences Fattouma Bourgiba Monastir.
For all patients included, a data collection form must be completed, mentioning age, sex, medical and surgical history, and the type of procedure planned.
If during the procedure the patient describes intolerable pain: the VAS will be noted, and the patient will use a rescue analgesic (intranasal ketamine or other at the discretion of the attending physician).
The VR device consists of a pair of VR glasses with a video previously chosen and installed. Patient preparation must be done before initiating the protocol.
The first step is to choose patient candidates for VR who are understanding and interested. Guardian approval is required; then it is necessary to explain the principle, the stages and the benefits of the care.
The intensity of pain is calculated according to the visual analog scale before, during the procedure and 30 minutes after as well as the max VAS during the procedure, the 'Children Fear Scale', the satisfaction score and any adverse effects are noted.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| VR device | Other | The VR device consists of a pair of VR glasses with a video previously chosen and installed. Patient preparation must be done before initiating the protocol. The first step is to choose patient candidates for VR who are understanding and interested. Guardian approval is required; then it is necessary to explain the principle, the stages and the benefits of the care. The intensity of pain is calculated according to the visual analog scale before, during the procedure and 30 minutes after as well as the max VAS during the procedure, the 'Children Fear Scale', the satisfaction score and any adverse effects are noted. |
| Measure | Description | Time Frame |
|---|---|---|
| frequency of success | frequency of success (%) (use of emergency analgesics) | 30 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| reduction of pain | reduction in pain assessed by the visual analog scale (mm) | 30 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| occurrence of adverse events and patient satisfaction | occurrence of adverse events, tolerance to glasses, patient satisfaction (Likert Satisfaction Scale) and max VAS during the procedure. | 3 hours |
Inclusion Criteria:
Exclusion Criteria:
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For all patients included, a data collection form must be completed, mentioning age, sex, medical and surgical history, and the type of procedure planned.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| NOUIRA Semir, PR | Contact | 73106000 | 216 | semir.nouira@rns.tn |
| GANNOUN IMEN, ARC | Contact | 73106000 | 216 | gannounimen@yahoo.fr |
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| ID | Term |
|---|---|
| D010146 | Pain |
| D001008 | Anxiety Disorders |
| D004204 | Joint Dislocations |
| ID | Term |
|---|---|
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D001523 | Mental Disorders |
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| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D014947 | Wounds and Injuries |