Skip to content

Difficult Intravenous Access Perception: Difficult IV Access - Assessment of Patient Understanding

Assessment of Patient Understanding and Preference of Rescue Venous Access When Shown a Narrated Video Vignette Versus Traditional Paper Information Sheet

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01929304
Acronym
DIVA
Enrollment
1180
Registered
2013-08-27
Start date
2013-08-31
Completion date
2016-07-31
Last updated
2023-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Understanding Emergency Room Procedures

Brief summary

Aim: Patient Perception: This aim broadly intends to use traditional script versus a brief video education vignette to determine understanding and preferences among general emergency department patients of rescue access techniques. A challenge of emergency care is providing patient education surrounding procedures in a standardized and patient-oriented manner. This data would provide insight on a patient's understanding of the risks and benefits of rescue access, assess patient preference, and potentially influence what rescue technique is employed in the future. This information may also give us insight onto why DIVA patients might refuse randomization.

Interventions

OTHERSurvey

Sponsors

University of Pennsylvania
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* greater than or equal to 18 years of age * fluent in English * hemodynamically stable emergency department patient

Exclusion criteria

* history of or current status of difficult intravenous access

Design outcomes

Primary

MeasureTime frameDescription
Patient UnderstandingBaselineAssess patients' understanding of and preferences regarding emergency department procedures: ultrasound-guided IV access and intra-osseous access.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026