- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00129064
Improving the Outpatient Referral Process With Electronic Communications
April 23, 2007 updated by: Brigham and Women's Hospital
An electronic referral application will be developed and integrated into the existing outpatient information system.
The primary goal of this software is to improve the quality and coordination of patient care by increasing physician-to-physician communication.
The investigators anticipate that improved communications will also enhance physician and patient satisfaction and provide cost savings.
These outcomes will be formally evaluated following implementation of the application.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
A trial will be performed to test and quantify the benefits of electronic referrals.
Primary care physicians (PCPs) from 2 community-based clinics will be recruited for enrollment.
The control group will initiate referrals using the pre-existing paper forms; physician-to-physician communication can occur by e-mail, phone, or mail at the discretion of the referring physician as is currently the standard.
Physicians randomized to the intervention arm will be asked to use the electronic application for every referral during the study period.
For 6 months, every new referral initiated within the study groups will be assessed for the completeness of patient information and timing of feedback to the referring physician via physician surveys.
In addition, a subgroup of patients in the control and intervention arms will be surveyed to assess the impact of the intervention on patient satisfaction with the referral process.
Study Type
Interventional
Enrollment
200
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Massachusetts
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Boston, Massachusetts, United States, 02115
- Brigham and Women's
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Any referral initiated by a PCP at the study sites for a patient to go to a specialist for the first time
Exclusion Criteria:
- Referrals for repeat specialist visits or referrals not initiated by a PCP
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
Percentage of referral requests with complete information
|
Percentage of referrals with timely information exchanged
|
Secondary Outcome Measures
Outcome Measure |
---|
Patient satisfaction
|
Physician satisfaction
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Tejal K Gandhi, MD, Brigham and Women's Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2005
Study Completion
March 1, 2007
Study Registration Dates
First Submitted
August 9, 2005
First Submitted That Met QC Criteria
August 9, 2005
First Posted (Estimate)
August 11, 2005
Study Record Updates
Last Update Posted (Estimate)
April 24, 2007
Last Update Submitted That Met QC Criteria
April 23, 2007
Last Verified
April 1, 2007
More Information
Terms related to this study
Other Study ID Numbers
- 2004-P-000710
- 20010373
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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