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Preprocedural, preoperative, and prevascular access anxiety in pediatric patients has been previously shown to increase the likelihood of family stressors, postoperative pain, agitation, sleep disturbances, and negative behavioral changes. The purpose of this study is to determine if a non-invasive distracting devices (Virtual Reality headset) is more effective than the standard of care (i.e., no technology based distraction) for preventing anxiety before vascular access among hospitalized children undergoing vascular access prior to anesthesia, procedures, surgery, blood draws, port access, or peripheral IV placement. The anticipated primary outcome will be reduction of child's anxiety during and after vascular access.
Anxiety among children undergoing vascular access is common. Not only is high anxiety traumatic, but research indicates that high anxiety in children before surgery leads to adverse outcomes such as increased pain and analgesics requirements, delayed hospital discharge, and maladaptive behavioral changes. Treating anxiety may decrease any of these undesirable behaviors.
In this study, investigators hope to determine if technology based distractions (VR headsets) are more effective than standard care for preventing high anxiety before vascular access. As a secondary aim of the study, we seek to determine if the use of technology based distraction will result in higher parent and patient satisfaction, decreased fear, and increased compliance, while monitoring for side-effects of the intervention.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control | No Intervention | The control group will be provided standard of care, which is no use of technologies. | |
| Intervention Group VR | Experimental | Interventional arm will use technology based distractions (Virtual Reality) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Technology Based Distractions | Behavioral | Technology based distractions (VR headsets) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Pain Score | Peak Pain Score minus Baseline Pain Score(0-10) | immediately post vascular access minus baseline |
| Measure | Description | Time Frame |
|---|---|---|
| Fear Score | Fear Faces | immediately post vascular access minus baseline |
| Family Satisfaction | Family Satisfaction Survey | Immediatly Post Vascular Access |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Samuel Rodriguez, MD | Stanford University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Lucile Packard Children's Hospital at Stanford | Palo Alto | California | 94304 | United States |
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| ID | Term |
|---|---|
| D013315 | Stress, Psychological |
| ID | Term |
|---|---|
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
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| Patient Satisfaction | Patient Satisfaction Survey | Immediately Post Vascular Access |
| Patient Compliance | Modified Induction Compliance Checklist | At the time of Vascular Access |
| Adverse Events | Negative outcomes such as nausea, headache | At the time of Vascular Access |