- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01301534
Comparison of Methods to Improve Abdominal Aortic Aneurysm (AAA) Screening Rates in the Primary Care Setting.
Study Overview
Status
Conditions
Detailed Description
Approximately 1700 male patients (DoD beneficiaries) between the ages of 65-75 will be selected from their medical records. The information on the attached abstracted data sheet will be collected. As part of standard patient care operations, the Family Medicine and Internal Medicine Departments will inform patients on the need to receive a AAA screening ultrasound, based on their primary care manager's (PCM) preference for clinical notification:
- Nurse initiated Telephone Consult (T-Con) (see attached)
- Mail-0ut Letter to the patient (see attached)
- Provider, Nurse and Technician Education with point-of-care patient referrals , Exam Room Flyer
- Control group (i.e. usual care)
The Provider, Nurse and Technician Education will consist of a presentation given by the Principal Investigator (see attached PowerPoint) to the Family Medicine and Internal Medicine clinic staff and the posting of Exam Room Flyers in each Family Medicine and Internal Medicine exam room to prompt and encourage patient referrals for a AAA screening ultrasound.
Information requested on the attached abstracted data sheet will be used for initial identification of patients that should have a AAA screening ultrasound and again 3-4 months later to see if these same individuals received the procedure. All informational data sets will be totally de-identified by the Research Coordinator, Nellis Air Force Base, prior to releasing to the Principle Investigator.
The data will then be analyzed by Dr. Anneke Bush (WHMC statistician) and the results will be provided to the Principal Investigator for analysis.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Nevada
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Nellis AFB, Nevada, United States, 89191
- Michael O'Callaghan Federal Hospital/Nellis Air Force Base
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion:
- Tricare Insurance Beneficiary (military insurance) receiving care at Nellis AFB
- Male patients (DoD beneficiaries) between the ages of 65-75 years old.
Exclusion:
- Female patients.
- Non-English speaking.
- Patients who have already had abdominal CT scan, abdominal MRI, aortography or aortic ultrasound.
- Patients already diagnosed with AAA
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
T-Con
1. Nurse initiated Telephone Consult (T-Con)
|
Mail-Out
2. Mail-0ut Letter to the patient
|
Education
3. Provider, Nurse and Technician Education with point-of-care patient referrals , Exam Room Flyer
|
Control group
4. Control group (i.e.
usual care)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
improving screening rates for AAA
Time Frame: 1 year
|
Will the concerted use of (1) a nurse-initiated telephone consult (T-Con), (2) mail out reminder or (3) provider, nurse and technician education with point-of-care reminders be more successful than usual care at improving screening rates for AAA?
|
1 year
|
Collaborators and Investigators
Investigators
- Principal Investigator: Ethan Zimmerman, M.D., Michael O'Callaghan Federal Hospital/Nellis Air Force Base
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FWH20110041H
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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