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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00368823
Other study ID # HS10516-03
Secondary ID
Status Completed
Phase Phase 3
First received August 24, 2006
Last updated August 24, 2006
Start date November 1999
Est. completion date December 2003

Study information

Verified date August 2006
Source University of Washington
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Does presentation of clinical evidence for decision making at point-of-care improve prescribing patterns in ambulatory pediatrics?


Description:

We showed previously that an electronic prescription writer and decision support system improved pediatric prescribing behavior for otitis media in an academic clinic setting. This study assessed whether point-of-care evidence delivery could demonstrate similar effects for a wide range of other common pediatric conditions. We performed a randomized controlled trial in a teaching clinic/clinical practice site and a primary care pediatric clinic serving a rural and semi-urban patient mix. There were 36 providers at the teaching clinic/practice site, and 8 providers at the private primary pediatric clinic, and an evidence-based message system presented real time evidence to providers based on prescribing practices for acute otitis media, allergic rhinitis, sinusitis, constipation, pharyngitis, croup, urticaria, and bronchiolitis. We measured the proportion of prescriptions dispensed in accordance with evidence.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date December 2003
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria: The 44 clinical providers at the two participating clinics. -

Exclusion Criteria: Study investigators

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Intervention

Device:
Electronic point-of-care delivery system


Locations

Country Name City State
United States Roosevelt Pediatric Clinic Seattle Washington
United States Skagit Valley Pediatrics Skagit Valley Washington

Sponsors (2)

Lead Sponsor Collaborator
University of Washington Agency for Healthcare Research and Quality (AHRQ)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary prescribing practices for acute otitis media,
Primary allergic rhinitis,
Primary sinusitis,
Primary constipation,
Primary pharyngitis,
Primary croup,
Primary urticaria,
Primary bronchiolitis
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