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Completed

NCT Number: NCT01398761

Development of a Sign-Out Tool to Improve Handoffs in Care

The purpose of this grant is to fund the research necessary to fully understand the impact of this sign-out tool on clinician workflow, quality of sign-out, and continuity of care. This information will inform exactly how Partners will move ahead with tools to improve handoffs in care (i.e., whether the prototype will be adapted further, adopted Partners wide, or abandoned in favor of other solutions). The investigators hypothesize that a web-based handoff tool improves provider satisfaction, the quality of written sign-outs, and measures of continuity of care compared with current handoff tools.

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Key information

Conditions

Continuity of Patient Care Quality of Signout Workflow

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Brigham & Women's Hospital

Boston, Massachusetts, 02115, United States

About this study

This study will attempt to answer the following questions:

  • What are the specific needs for clinical content among various clinical personnel (nurses, residents, and attendings) on different services at two different hospitals (MGH, BWH)?
  • How can IT support sign-out that facilitates interdisciplinary communication and yet preserves user-specific content among different clinical personnel?
  • Can a sign-out tool currently deployed at MGH be transferred to BWH using existing IT services and a minimum amount of local IS effort?
  • What will be the future needs of this tool so that it can fully access data from MetaVision once it is deployed?
  • How should the tool be further improved such that it optimizes user adoption, provider satisfaction and workflow, the quality of sign-out, and continuity of care?
  • Is it feasible for a future, refined version of this tool to be adopted across Partners acute care hospitals?

The study design is an observational, before-after pilot study. A multi-disciplinary steering committee and working group will be assembled to determine requirements and guide design in conjunction with HPM leadership, research staff, a Partners IS analyst, and MGH LCS personnel. The intervention will then be implemented on two services. Before and during implementation, several outcomes will be measured, including provider satisfaction and workflow, continuity of care, and quality of sign-out.

Deliverables will include the following:

  • Clinical and functional specifications for a new web-based sign-out tool
  • A prototype of the sign-out tool tested on 2 active clinical services, one each at MGH and BWH
  • A report of the impact of the tool on clinical care
  • Lessons learned regarding design and implementation that can be applied to more broad-based efforts
  • An update to the Sign-out White Paper with recommendations for action based on the results of this study The lessons learned will be applicable not only to Partners, but to other institutions (nationwide and worldwide) wishing to improve patient safety during handoffs in care.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • All nurses, residents, PAs, and attendings on the two study services

Exclusion criteria

  • Clinical staff not on study services within study period

Treatment and study plan

Signout tool

Other

Electronic signout tool

Primary outcomes

  1. Proportion of required data elements present

    Time frame: 8 months

    The proportion of required data elements present in written/typed sign-outs during tool implementation.

Secondary outcomes

  1. Direct observations

    Time frame: 8 months

    Time spent preparing and delivering sign-out will be compared before and after implementation of the sign-out using linear regression clustered by user.

  2. User satisfaction

    Time frame: 8 months

    Individual questions from the user satisfaction survey will be presented as medians with interquartile ranges on Likert-type questions and compared using the Wilcoxon rank sum test. A global satisfaction score will be derived by calculating the proportion of questions for which users were satisfied or very satisfied, and compared using linear regression. Results of the continuity of care survey will be analyzed similarly.

Sponsors and collaborators

Lead sponsor

Brigham and Women's Hospital

Other

Collaborators

  • Partners Siemens Research Council

Registry information

Official study title

Development and Pilot Testing of a Web-Based, Multi-Disciplinary Sign-Out Tool to Improve Handoffs in Care

Important dates

Study start
2011
Primary completion
2011
Study completion
2011
First posted
Jul 21, 2011
Registry last updated
Apr 28, 2014

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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