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Notation Optimization Through Template Engineering (NOTE)

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Johns Hopkins University

Status

Completed

Conditions

Clinical Documentation

Treatments

Other: Standard progress note template
Other: New progress note template

Study type

Interventional

Funder types

Other

Identifiers

NCT04333238
IRB00117171

Details and patient eligibility

About

This is a randomized non-blinded controlled trial of a standard note template versus a redesigned note template using a simulated patient encounter and the electronic medical record.

Full description

Residents documented the simulated patient encounter using one of two templates. The standard template was based on the usual outpatient progress note. The new template placed the assessment and plan section in the beginning, grouped subjective data into the assessment section, and deemphasized elements not related to the current presentation.

Enrollment

36 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Residents who had open visit slots during their outpatient clinic time

Exclusion criteria

  • None

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 2 patient groups

Standard template
Active Comparator group
Description:
Usual outpatient progress note with standard Subjective Objective Assessment Plan (SOAP) format
Treatment:
Other: Standard progress note template
New template
Experimental group
Description:
The assessment and plan section is placed in the beginning, subjective data grouped into the assessment section, and elements not related to the current presentation were deemphasized
Treatment:
Other: New progress note template

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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