Problem Specific Templates for Electronic Hospital Documentation

NCT ID: NCT01958723

Last Updated: 2015-04-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-11-30

Study Completion Date

2014-07-31

Brief Summary

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The emergence of electronic documentation has led to multiple new challenges for physicians. Despite positive expectations, many physicians have received electronic health systems with mixed results. Review of current literature has identified the following reasons for concern: increased time required for documentation, deteriorating quality of notes, mindless use of copy-and-paste functions, and fragmentation of clinical work from poorly designed computing workflows. The study of template use has not been done in a large scale or with clear outcome measurements. The purpose of this study is to examine the effects of Problem Specific Templates on quality, accuracy, and efficiency of physician documentation practices.

Detailed Description

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This is a prospective cohort study, which will examine the effects of Problem Specific Templates on quality, accuracy, and efficiency of physician documentation practices. The Hospitalist physicians will be the subjects. All physicians of the Hospital Medicine Service will be invited to participate. For the intervention, participating Hospitalists will be trained on the use of templates for 20 common hospital problems. Once trained, the Hospitalists will be asked to use these templates for a one-month period. Pre-intervention and post-intervention medical records will be compared using chart reviews, validated document assessment instruments, physician surveys, and electronic medical record time auditing.

Conditions

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Quality/Accuracy of Physician Documentation Efficiency of Physician Documentation

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Hospitalists

Introduction of Problem Specific Templates

Hospitalists

Intervention Type OTHER

Introduction of Problem Specific Templates

Interventions

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Hospitalists

Introduction of Problem Specific Templates

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Physicians: All physicians of the Hospital Medicine Service will be invited to participate

Exclusion Criteria

* Any invited physicians who refuse to consent
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Florida

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Raj Mehta, M.D.

Role: PRINCIPAL_INVESTIGATOR

University of Florida

Robert Leverence, M.D.

Role: STUDY_CHAIR

University of Florida

Locations

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University of Florida

Gainesville, Florida, United States

Site Status

Countries

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United States

Other Identifiers

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201300232

Identifier Type: -

Identifier Source: org_study_id

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