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Completed

NCT Number: NCT02301793

Educating Nurses About Venous Thromboembolism (VTE) Prevention

As part of mandatory on-going nursing education, the investigators have incorporated identical information into two distinct web-based learning formats - the traditional linear PowerPoint format (with voice-over) and a new interactive format developed with central nursing education.

The investigators will cluster randomize nurses by floor to receive either the traditional education or the new interactive education, and evaluate the impact on administration of VTE prophylaxis doses administered by nurses before and after education. All nurses on a floor will receive the same educational format. If one method of education results in statistically significant improvement in VTE prophylaxis administration, the investigators will cross over to deliver the superior education format to all nurses who originally were given the less effective method.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Johns Hopkins Medical Institutions

Baltimore, Maryland, 21287, United States

About this study

BACKGROUND

  • In an attempt to improve venous thromboembolism (VTE) prophylaxis adherence the investigators carried out qualitative studies to obtain patients' viewpoints on how nurses should be educated about VTE prevention and to assess nurses' beliefs and perceptions about pharmacologic VTE prophylaxis
  • The investigators observed deficiencies in nurses' knowledge and misconceptions about VTE prophylaxis that likely lowers adherence to administration of prescribed VTE prophylaxis doses
  • As a part of our original Patient-Centered Outcomes Research Institute (PCORI) proposal, the investigators planned to educate nurses to address the observed deficiencies and misconceptions and improve their ability to communicate effectively with patients
  • Historically, nurse education has been done via a linear, PowerPoint-based platform with voice-over but with no interactive component (TRADITIONAL)
  • A newer platform for nurse education became available for use and includes scenario-based teaching, ongoing assessment, and immediate remediation. Most importantly, it is a highly interactive product (CONTEMPORARY)

STUDY DESIGN AND ANALYTIC PLAN

  • Research hypotheses
  • Primary: Nurse participants who receive either of these interventions will improve administration of prescribed VTE prophylaxis evidenced by a decrease in frequency of non-administered doses of VTE prophylaxis, compared with their frequency at baseline.
  • Secondary: Nurse participants who receive the contemporary education format will have a larger decrease in frequency of missed doses of VTE prophylaxis compared with those who participate in the traditional education format.
  • Study Design
  • Cluster Randomized Trial 21 floors, block randomized by floor type (medicine [n=11] vs. surgery [n=10]) and (ICU [n=5] vs. non-ICU [n=16]) All nurses on each floor are assigned the same education type to mitigate issues related to contamination if nurses discuss the education with their colleagues
  • Primary Outcome measure: Proportion of non-administered doses of pharmacological VTE prophylaxis (dose level)
  • Secondary Outcome Measures:
  • Proportion of doses documented as missed due to patient refusal (dose level)
  • Proportion of patients with any VTE (patient level)
  • Proportion of patients with Deep Vein Thrombosis (DVT) (patient level)
  • Proportion of patients with Pulmonary Embolism (PE) (patient level)
  • Analytic methods
  • Primary analyses - Intention-to-treat (includes all nurses assigned, whether or not they completed the education) Is there a difference between units allocated to either of the interventions comparing their outcome measure to their baseline measure? Is there a difference comparing those who received the contemporary education format vs. the traditional education format?
  • Secondary analysis - Per protocol (includes only nurses who completed the education) Do nurses who receive education perform better (improved administration of prescribed VTE prophylaxis) than those who did not? Do nurses who received the education in the contemporary format perform better than those who received it in the traditional format

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Nurses on selected surgical and medical floors at Johns Hopkins Hospital

Exclusion criteria

  • Nurses who were not permanently associated with one of the 21 hospital floors (e.g. traveling nurse, float nurse) were excluded from this study

Treatment and study plan

Nurse education in contemporary format

Behavioral

Education about VTE was delivered through a web-based contemporary interactive format

Nurse education in traditional format

Behavioral

Education about VTE was delivered through a web-based traditional linear Powerpoint format with voice over.

Primary outcomes

  1. Non Administration of Prescribed VTE Prophylaxis Medication Doses

    Time frame: (Baseline); approximately 3 months later (Post-Education)

    This is the percentage of VTE prophylaxis doses that were not administered for any reason as documented in the electronic health record by a nurse

Secondary outcomes

  1. Rates of All VTE Among Hospitalized Patients

    Time frame: 3-12 months after end of study

    Did the intervention decrease rates of VTE among hospitalized patients?

  2. Rates of Deep Vein Thrombosis (DVT) Among Hospitalized Patients

    Time frame: 3-12 months after end of study

    Did the intervention decrease rates of DVT among hospitalized patients?

  3. Rates of Pulmonary Embolism (PE) Among Hospitalized Patients

    Time frame: 3-12 months after end of study

    Did the intervention decrease rates of PE among hospitalized patients?

  4. Proportion of Non Administration of Prescribed VTE Prophylaxis Medication Doses Which Are Documented as Patient Refusal

    Time frame: Baseline; approximately 3 months later (post education)

    Did the intervention decrease rates of patient refusal of VTE prophylaxis medication doses among hospitalized patients?

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • Patient-Centered Outcomes Research Institute

Registry information

Official study title

Educating Nurses About Venous Thromboembolism Prevention

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Nov 26, 2014
Registry last updated
May 17, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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