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OpenTrials
Completed

NCT Number: NCT01855646

Improved Patient Handoffs to Prevent Sentinel Events

The overall aim of this project is to improve the quality of the handoffs between hospitalists on the general medicine service at Durham Regional Hospital with the intent of improving transitions of care. The intervention will be an improved and more structured face to face sign-out process using a standardized admission sign-out sheet, which is not part of the official medical record. Daytime admitting physicians will assign an acuity score to their patients in which the severity of illness will be scored from 1-7, with 7 being the most sick / likely to have rapid response team (RRT) or adverse event. The assignment of this score would be based off of the clinician's judgment in the patient's overall assessment. All patients, age >18 years, admitted to the non-resident hospital medicine general medicine service at DRH will be study eligible. Data analysis will examine aggregate hospitalist perception of sign-out practice before and after intervention, total number of RRTs, unplanned transfers, and rapid responses pre and post intervention, percentage of hospitalist based patients of overall rapid responses pre and post intervention, percentage of hospitalists using acuity scores, and average and mean severity score of patients with rapid responses compared with those admitted. Patients have a risk of loss of confidentiality.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Durham Regional Hospital

Durham, North Carolina, 27704, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • patients age >18 years
  • admitted to the non-resident hospital medicine general medicine service at Durham Regional Hospital (DRH). (This would include transfers from outside hospital, the Emergency Room, intensive care units, and the Durham Rehab Institute.)
  • Additionally, hospital medicine faculty who round on the non-resident general medicine service at DRH will be included for the purposes of completion of perception surveys.

Exclusion criteria

  • Patients presenting for consults, rapid responses handled by surgical services and rapid responses as reason for transfer from Durham Rehabilitation Institute.

Treatment and study plan

Structured Sign Out Form

Other

Primary outcomes

  1. Comparison of RRT's and unplanned transfers pre and post intervention matching aggregate numbers month to month

    Time frame: End of Study, Approximately 6 months

Secondary outcomes

  1. Physician attitudes towards sign-out process pre and post intervention

    Time frame: End of Study, Approximately 6 months

Other outcomes

  1. Compliance rate monthly with sign-out sheet completion; will use simple descriptive statistics

    Time frame: End of Study, Approximately 6 months

Sponsors and collaborators

Lead sponsor

Duke University

Other

Registry information

Official study title

Patient Acuity Score With Improved Patient Handoffs to Prevent Sentinel Events

Important dates

Primary completion
2014
Study completion
2014
First posted
May 16, 2013
Registry last updated
Nov 25, 2016

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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