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This study, titled "R.A.G.A.Z.: Virtual Reality for Reducing Anxiety and Pain in Pediatric Orthopedic Surgery," aims to see if using virtual reality (VR) can help children feel less anxious and experience less pain during minor orthopedic surgeries. The research will compare the effects of VR to the usual pre-surgery sedative medication.
**Study Hypotheses**
The researchers hypothesize that using VR will:
1. Reduce anxiety levels in children before and after surgery compared to standard sedative medication.
**Who can participate?**
**Study Process**
Participants will be randomly assigned to one of two groups:
The study will measure:
The study is being conducted by IRCCS - Istituto Ortopedico Rizzoli in Bologna, Italy. It is a non-profit study funded by donations.
The goal is to find out if VR can reduce the need for sedatives, decrease anxiety and pain, and improve the overall surgical experience for children.
**Detailed Description**
This study, titled "R.A.G.A.Z.: Virtual Reality for Reducing Anxiety and Pain in Pediatric Orthopedic Surgery," aims to evaluate the effectiveness of virtual reality (VR) in reducing perioperative anxiety and pain in children undergoing minor orthopedic surgeries. The study will compare the use of VR headsets to the traditional method of pre-surgery sedation with medication.
**Purpose of the Study**
The primary objective of this study is to determine whether VR can provide better control of anxiety in pediatric patients before and after anesthetic and surgical procedures. The study will also assess whether VR can reduce the need for sedative and pain-relief medications, thereby minimizing potential side effects and improving recovery times.
**Study Hypotheses**
The researchers hypothesize that VR will:
**Study Design**
This is a non-profit, randomized controlled trial conducted at the IRCCS - Istituto Ortopedico Rizzoli in Bologna, Italy. The study will include 50 children aged 7 to 12 years, who are candidates for minor orthopedic surgeries lasting less than 60 minutes. Participants will be randomly assigned to one of two groups:
**Procedures**
**Expected Outcomes**
The study aims to demonstrate that VR can effectively reduce perioperative anxiety and pain, leading to a lower requirement for sedatives and analgesics. By providing a non-pharmacological method to manage anxiety and pain, VR could improve the overall surgical experience for pediatric patients and enhance recovery outcomes. Additionally, the study seeks to validate the feasibility and acceptability of VR as a standard practice in pediatric surgical settings.
**Study Timeline**
The study is expected to last 24 months, including patient enrollment, data collection, and analysis. Each participant will be involved from the preoperative visit through the first 24 hours post-surgery. The results will be analyzed and published to contribute to the growing body of evidence supporting the use of VR in medical procedures.
**Ethical Considerations**
The study will be conducted following the principles of the Declaration of Helsinki and Good Clinical Practice (GCP) guidelines. Informed consent will be obtained from all participants and their parents or guardians. The privacy and confidentiality of all participants will be strictly maintained.
This study has the potential to revolutionize the approach to managing perioperative anxiety and pain in pediatric patients, offering a safe, effective, and enjoyable alternative to traditional sedative medications.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| control | No Intervention | pre-surgery sedation | |
| VR | Experimental | virtual reality sedation |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| hypno VR | Device | pre-surgery sedation using virtual reality headset |
|
| Measure | Description | Time Frame |
|---|---|---|
| anxiety level | level of anxiety with cam-s | 24 hours |
| Measure | Description | Time Frame |
|---|---|---|
| hormons levels | levels of stress hormons | preoperative |
| pain level | difference in pain levels | 24 hours |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Istituto Ortopedico Rizzoli | Recruiting | Bologna | Italy |
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| compliance during induction | compliance during induction of anesthesia with micc | during induction |
| drugs dosage | dosage of drugs necessary for induction of anesthesia | intraoperative |
| surgeons satisfaction | general satisfaction of the surgeons from 1 to 10 | immediately after the intervention |
| parents satisfaction | general satisfaction of the parents from 1 to 10 | immediately after the intervention |
| or time occupation | time of occupation of the or | intraoperative |
| adverse event | adverse avent using virtual reality | 24 hours |