Clinical Trials Directory

Trials / Completed

CompletedNCT03220828

Evaluation of Technology-Based Stress Reduction Techniques Prior to Vascular Access

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
220 (actual)
Sponsor
Stanford University · Academic / Other
Sex
All
Age
7 Years – 18 Years
Healthy volunteers
Accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALTechnology Based DistractionsTechnology based distractions (VR headsets)

Timeline

Start date
2017-08-01
Primary completion
2019-03-31
Completion
2019-03-31
First posted
2017-07-18
Last updated
2019-04-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03220828. Inclusion in this directory is not an endorsement.