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NCT03220828 · ClinicalTrials.gov registry record · NA

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

A NA study of Stress, Emotional, sponsored by Stanford University.

Completed
Registry status
NA
Development phase
220
Enrollment target
1
Study location

NCT03220828 is a NA study of Stress, Emotional that has completed, run by Stanford University. The registered enrollment target is 220 participants, below the 350-participant average among 7 other Stress, Emotional trials with a reported enrollment target (37% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03220828, a NA study of Stress, Emotional, has completed, sponsored by Stanford University.

COMPLETED
Registry status
NA
Development phase
220 participants
Enrollment target
1
Study location

Study 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.

Conditions Studied

Interventions

  • BEHAVIORAL Technology Based Distractions

Study Locations (1)

California

  • Lucile Packard Children's Hospital at Stanford - Palo Alto

Trial Details

FieldValue
Enrollment Target 220 participants
Start Date 2017-08-01
Est. Completion 2019-03-31
Phase NA

Sponsor

Stanford University

1,744 total trials

What the Registry Record Tells You About NCT03220828

The ClinicalTrials.gov registry entry for NCT03220828 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 220 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 350-participant average among 7 other Stress, Emotional trials with a reported enrollment target (37% lower). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Stress, Emotional appearing as the primary indexed condition, and to 1 intervention - of which Technology Based Distractions is the first listed.

NCT03220828 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT03220828 about?

NCT03220828 is a clinical study titled "Evaluation of Technology-Based Stress Reduction Techniques Prior to Vascular Access". 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 ...

What is the current status of trial NCT03220828?

This trial is currently completed. It is a NA study. The enrollment target is 220 participants. The study started on 2017-08-01. Estimated completion is 2019-03-31.

What conditions does trial NCT03220828 study?

This clinical trial studies the following conditions: Stress, Emotional.

What interventions are being tested in trial NCT03220828?

The interventions under investigation include: Technology Based Distractions (BEHAVIORAL).

Who is sponsoring clinical trial NCT03220828?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03220828 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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