Impact of Continuing Medical Education (CME) Insulin Program
NCT ID: NCT00824603
Last Updated: 2015-12-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
294 participants
OBSERVATIONAL
2006-06-30
2009-08-31
Brief Summary
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Detailed Description
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Question 1. Clinical guidelines. Is insulin initiated earlier (at a lower A1C)?
Question 2. Decision-making. Does confidence in selecting a starting insulin regimen change? Does confidence in selecting a starting insulin dose change? Does confidence in adjusting insulin change? Does confidence in discussion nutrition guidelines change?
Question 3. Application. Do more patients start using insulin? Who usually selects starting dose? How is starting dose selected? How often is insulin adjusted?
Question 4. Resources. How available are protocols for insulin use? How available is adequate time to monitor insulin therapy? How available is staff to teach insulin injections? How available is staff to help adjust insulin?
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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primary care provider
attending insulin CME Training
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
25 Years
ALL
Yes
Sponsors
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International Diabetes Center at Park Nicollet
OTHER
Eli Lilly and Company
INDUSTRY
Novo Nordisk A/S
INDUSTRY
United Health Care
UNKNOWN
Merck Sharp & Dohme LLC
INDUSTRY
HealthPartners Institute
OTHER
Responsible Party
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Principal Investigators
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Margaret Powers, PhD
Role: PRINCIPAL_INVESTIGATOR
International Diabetes Center at Park Nicollet
Locations
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International Diabetes Center
Minneapolis, Minnesota, United States
Countries
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Other Identifiers
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03425-06-C
Identifier Type: -
Identifier Source: org_study_id