NCT01043133

Brief Summary

The purpose of the study is to measure the effectiveness of a social marketing-based medical education intervention on student use of evidence-based templates for documenting outpatient asthma care within an electronic medical record.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
155

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jul 2009

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2009

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

January 5, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 6, 2010

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2010

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2010

Completed
1.2 years until next milestone

Results Posted

Study results publicly available

August 12, 2011

Completed
Last Updated

August 12, 2011

Status Verified

January 1, 2010

Enrollment Period

11 months

First QC Date

January 5, 2010

Results QC Date

December 3, 2010

Last Update Submit

July 14, 2011

Conditions

Keywords

electronic medical recordsdocumentation templatesclinical encounter notes

Outcome Measures

Primary Outcomes (1)

  • Number of Participants Using Evidence-based Template to Document Asthma Care Within an Electronic Medical Record

    The primary outcome measure is a count of whether or not the research participant uses the electronic health record-based Asthma AIM form to document a simulated outpatient mild persistent asthma encounter at T1 (immediately following intervention) and T2 (upon completion of family medicine clerkship approximately 35 days later).

    immediately after invervention and 30+ days in follow-up

Secondary Outcomes (1)

  • Clinical Note Completeness Score

    immediately after intervention and 30+ days in follow-up

Study Arms (2)

Intervention group

EXPERIMENTAL
Behavioral: social marketing-based medical education intervention

Control Group

NO INTERVENTION

Interventions

social-marketing based medical education intervention designed to influence medical student use of evidence-based templates. Led by physician instructor.

Also known as: persuasion
Intervention group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Third year medical student completing family medicine clerkship Uniformed Services University

You may not qualify if:

  • All students other than those listed above

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Disease

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Results Point of Contact

Title
Ronald W. Gimbel
Organization
USUHS

Study Officials

  • Mark B. Stephens, MD, MS

    Uniformed Services University of the Health Sciences

    STUDY DIRECTOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
FED

Study Record Dates

First Submitted

January 5, 2010

First Posted

January 6, 2010

Study Start

July 1, 2009

Primary Completion

June 1, 2010

Study Completion

June 1, 2010

Last Updated

August 12, 2011

Results First Posted

August 12, 2011

Record last verified: 2010-01