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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01269736
Other study ID # 0711003292
Secondary ID R01HL081642
Status Completed
Phase N/A
First received January 3, 2011
Last updated August 28, 2017
Start date August 2008
Est. completion date March 2014

Study information

Verified date June 2017
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to test the effect of implementing new practice standards for electrocardiographic (ECG) monitoring on nurses' knowledge and skills, quality of care, and patient outcomes. The investigators hypothesize that increased knowledge and skills of nurses will lead to enhanced quality of care, which will result in improved outcomes for patients.


Description:

Despite advances in hospital electrocardiographic (ECG) monitoring technology, monitoring practices are inconsistent and often inadequate. The investigators recently published practice standards for ECG monitoring. The primary purpose of this 5-year multisite randomized clinical trial is to test the effect of implementing these standards on nurses' knowledge and skills, quality of care, and patient outcomes. The investigators expect that increased knowledge and skills of nurses will lead to enhanced quality of care, which will result in improved outcomes for patients. Units serving cardiac patients in 17 hospitals will participate. Hospitals will be randomized to the experimental or control group after baseline measures of knowledge and skills, quality of care, and patient outcomes are obtained. The intervention will include ECG monitoring education and strategies to implement and sustain change. The online education will include 4 modules: essentials of ECG monitoring, arrhythmia monitoring, ischemia monitoring, and QT interval monitoring. The strategies to implement and sustain change in the clinical area include reinforcement of education, incentives, and the designation of "champions" on each unit who will actively promote the implementation of the practice standards.


Recruitment information / eligibility

Status Completed
Enrollment 92057
Est. completion date March 2014
Est. primary completion date March 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Nurses (and monitor technicians): All nurses (and monitor technicians) working on participating units serving patients with cardiac disease

- Patients: All patients cared for on participating units

Exclusion Criteria:

- Nurses (and monitor technicians): No nurses (or monitor technicians) will be excluded

- Patients: No patients on the participating units will be excluded, even if their primary diagnosis is not cardiac

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Education
Online ECG monitoring education program and strategies to implement and sustain change for nurses

Locations

Country Name City State
Canada University of Ottawa Heart Institute, Ottawa, Canada Ottawa Ontario
China Hong Kong Sanatorium & Hospital Hong Kong
United States Seton Medical Center Austin Texas
United States Erie County Medical Center Buffalo New York
United States Aultman Hospital Canton Ohio
United States University of North Carolina Hospitals Chapel Hill North Carolina
United States Baylor University Medical Center Dallas Texas
United States Long Beach Memorial Medical Center Long Beach California
United States Meriter Heart Hospital Madison Wisconsin
United States Yale-New Haven Hospital New Haven Connecticut
United States Hospital of the University of Pennsylvania Philadelphia Pennsylvania
United States Thomas Jefferson University Hospital Philadelphia Pennsylvania
United States Maine Medical Center Portland Maine
United States United Hospital Saint Paul Minnesota
United States University of California, San Francisco Medical Center San Francisco California
United States Baystate Medical Center Springfield Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Yale University National Heart, Lung, and Blood Institute (NHLBI)

Countries where clinical trial is conducted

United States,  Canada,  China, 

References & Publications (3)

Funk M, Fennie KP, Stephens KE, May JL, Winkler CG, Drew BJ; PULSE Site Investigators. Association of Implementation of Practice Standards for Electrocardiographic Monitoring With Nurses' Knowledge, Quality of Care, and Patient Outcomes: Findings From the — View Citation

Funk M, Rose L, Fennie K. Challenges of an Internet-based education intervention in a randomized clinical trial in critical care. AACN Adv Crit Care. 2010 Oct-Dec;21(4):376-9. doi: 10.1097/NCI.0b013e3181e6765d. — View Citation

Funk M, Winkler CG, May JL, Stephens K, Fennie KP, Rose LL, Turkman YE, Drew BJ. Unnecessary arrhythmia monitoring and underutilization of ischemia and QT interval monitoring in current clinical practice: baseline results of the Practical Use of the Lates — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Nurses' Knowledge and Skills Related to ECG Monitoring Participants took a 20-item online test on essentials of ECG monitoring, and arrhythmia, ischemia, and QT interval monitoring. Scores represent the percentage of correct answers. (Test scores range from 0 to 100 with higher scores representing more correct answers) Baseline, 15 months, 30 months
Secondary Quality of Patient Care Related to ECG Monitoring Percentage of patients with accurate electrode placement, accurate rhythm interpretation, cardiac arrest, cardiac arrest initiated by arrhythmia, appropriate monitoring, telemetry units only, ST-segment monitoring when indicated, and QTc measurement when indicated Baseline, 15 months, 30 months
Secondary Patient Outcomes Mortality, in-hospital MI, and not surviving a cardiac arrest were obtained using administrative data and laboratory data (eg, troponin, CK-MB) for all patients. Mortality was defined as death that occurred on one of the participating units. To identify the occurrence of in-hospital MI, laboratory data, timing of procedures, and location of patient at the time of the first blood draw indicating the event were used. Cardiac arrest was defined as an event initiated by an arrhythmia that required immediate intervention and was initiated on a PULSE participating unit. For each qualifying cardiac arrest, it was determined whether the patient survived the event. Baseline, 15 months, 30 months
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