IIPE-PRIS Accelerating Safe Signouts

NCT02403466 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 875

Last updated 2015-03-31

No results posted yet for this study

Summary

Because communication and handoff failures are a root cause of two-thirds of "sentinel events"- serious, often fatal preventable adverse events in hospitals improving handoffs has been identified by AHRQ and the Joint Commission as a priority in nationwide efforts to improve patient safety. Comparative Effectiveness Research on handoff tools and processes has identified specific strategies to improve handoffs and reduce medical errors: 1) team training; 2) verbal mnemonics; and 3) use of written/computerized tools to supplement verbal sign-outs. To accelerate residents' use of CER-based handoff practices and improve patient safety, the investigators are implementing the three inventions above as a Resident Handoff Bundle (RHB) in eight pediatric hospitals in the United States and Canada.

Conditions

  • Serious Medical Errors
  • Resident Sign-out

Interventions

BEHAVIORAL

Resident Handoff Bundle

1\) team training, 2) verbal mnemonics, and 3) standardization of written/computerized handoff tools

Sponsors & Collaborators

  • Lucile Packard Children's Hospital

    collaborator OTHER
  • University of California, San Francisco

    collaborator OTHER
  • Primary Children's Hospital

    collaborator OTHER
  • St. Louis Children's Hospital

    collaborator OTHER
  • Children's Hospital Medical Center, Cincinnati

    collaborator OTHER
  • St. Christopher's Hospital for Children

    collaborator OTHER
  • Walter Reed National Military Medical Center

    collaborator FED
  • The Hospital for Sick Children

    collaborator OTHER
  • OHSU Doernbecher Children's Hospital

    collaborator OTHER
  • Boston Children's Hospital

    lead OTHER

Principal Investigators

  • Christopher P Landrigan, MD, MPH · Boston Children's Hospital

  • Amy J Starmer, MD, MPH · Oregon Health and Sciences University

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2013-05-31
Completion
2013-08-31

Countries

  • United States
  • Canada

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02403466 on ClinicalTrials.gov