NCT00915291

Brief Summary

The purpose of this study is to determine whether physicians can be educated to better handle inappropriate requests from patients for direct-to-consumer advertised prescription medications.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
133

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2007

Geographic Reach
1 country

4 active sites

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

May 1, 2007

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2008

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

June 5, 2009

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 8, 2009

Completed
Last Updated

June 8, 2009

Status Verified

June 1, 2009

Enrollment Period

1.4 years

First QC Date

June 5, 2009

Last Update Submit

June 5, 2009

Conditions

Keywords

medical educationclinical decisionmakingpharmaceutical marketing

Outcome Measures

Primary Outcomes (1)

  • Decision to prescribe celecoxib

Study Arms (2)

Usual education

NO INTERVENTION

Participants randomized into the "no intervention" arm were not exposed to the web-based educational modules

Web-based educational modules

EXPERIMENTAL

Participants randomized into the intervention arm were exposed to the web-based educational modules

Other: Web-based educational modules

Interventions

Interactive case-based modules that includes video vignettes of clinical interactions between hypothetical patients interacting with physicians

Web-based educational modules

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Resident physicians in internal medicine or family medicine specialties at participating study sites

You may not qualify if:

  • Completed less than 10 months of residency

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (4)

Stanford University School of Medicine

Stanford, California, 94305, United States

Location

Creighton University School of Medicine

Omaha, Nebraska, 68131, United States

Location

University of Pennsylvania School of Medicine

Philadelphia, Pennsylvania, 19104, United States

Location

University of Texas at Houston Medical School

Houston, Texas, 77030, United States

Location

Study Officials

  • Audiey C Kao, MD, PhD

    American Medical Association

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
CARE PROVIDER
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

June 5, 2009

First Posted

June 8, 2009

Study Start

May 1, 2007

Primary Completion

October 1, 2008

Study Completion

October 1, 2008

Last Updated

June 8, 2009

Record last verified: 2009-06

Locations