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A Trial of Point of Care Information in Ambulatory Pediatrics

A Randomized Clinical Trial to Improve Prescribing Patterns in Ambulatory Pediatrics

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00368823
Enrollment
44
Registered
2006-08-29
Start date
1999-11-30
Completion date
2003-12-31
Last updated
2006-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Otitis Media, Allergic Rhinitis, Bronchiolitis, Constipation, Croup, Pharyngitis, Sinusitis, Urticaria

Keywords

point of care, evidence based medicine

Brief summary

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

Detailed 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.

Interventions

DEVICEElectronic point-of-care delivery system

Sponsors

Agency for Healthcare Research and Quality (AHRQ)
CollaboratorFED
University of Washington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
0 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

The 44 clinical providers at the two participating clinics. -

Exclusion criteria

Study investigators \-

Design outcomes

Primary

MeasureTime frame
prescribing practices for acute otitis media,
allergic rhinitis,
sinusitis,
constipation,
pharyngitis,
croup,
urticaria,
bronchiolitis

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026