Proactive Reduction of Outpatient Malpractice: Increasing Safety, Efficiency, and Satisfaction

NCT01758315 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 213

Last updated 2013-01-01

No results posted yet for this study

Summary

The purpose of the Proactive Reduction of Outpatient Malpractice: Increasing Safety, Efficiency, and Satisfaction (PROMISES) project is to assemble a high-level Massachusetts consortium to test the impact of powerful quality improvement techniques to accomplish innovations and improvements in high risk ambulatory malpractice areas. We will target problem-prone processes in 3 areas of identified risk: 1) medication management, 2) test ordering and results management 3) follow-up and referral management.

Conditions

  • Medical Malpractice
  • Patient Safety

Interventions

OTHER

Training and in-office coaching

Participating practices will be coached to perform rapid, small-scale tests of change and to iteratively improve performance of problem-prone care systems, as well as to imbed simple measurement in routine daily work streams to guide improvement efforts. The sixteen intervention practices will serve as realistic research laboratories to help advance malpractice risk prevention and patient safety in specific areas by refining tools and strategies for smaller practices.

Sponsors & Collaborators

  • Brigham and Women's Hospital

    collaborator OTHER
  • Massachusetts Coalition for the Prevention of Medical Errors

    collaborator OTHER
  • Institute for Healthcare Improvement

    collaborator OTHER
  • Massachusetts Medical Society

    collaborator OTHER
  • Healthcare for All

    collaborator UNKNOWN
  • Crico

    collaborator OTHER
  • Coverys

    collaborator UNKNOWN
  • Agency for Healthcare Research and Quality (AHRQ)

    collaborator FED
  • Massachusetts Department of Health

    lead OTHER_GOV

Principal Investigators

  • Madeleine Biondolillo, MD · Massachusetts Department of Health

  • Gordon Schiff, MD · Brigham and Women's Hospital

  • Nicholas Leydon, MPH · Massachusetts Department of Health

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-07-31
Primary Completion
2013-06-30
Completion
2013-06-30

Countries

  • United States

Study Locations

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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 NCT01758315 on ClinicalTrials.gov