- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01875068
A Program of Physician Supervision to Improve the Quality of Patient Referrals From Nurse Practitioners and Physician Assistants
October 1, 2019 updated by: William C. Mundell, M.D., Mayo Clinic
Implementing a Program of Physician Supervision to Improve the Quality of Patient Referrals From Nurse Practitioners and Physician Assistants
The investigators have previously demonstrated utilizing a validated tool, that the quality of referrals from nurse practitioners (NP) and physician assistants (PA) is less than referrals from physicians.
The investigators hypothesize that with local physician input, the quality of referrals from nurse practitioners and physician assistants will improve.
This is a prospective study comparing patient referrals from nurse practitioners and physician assistants with and without prior discussion with a local physician.
Study Overview
Status
Terminated
Conditions
Study Type
Interventional
Enrollment (Actual)
42
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
-
-
Minnesota
-
Rochester, Minnesota, United States, 55905
- Mayo Clinic in Rochester
-
-
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
All nurse practitioners and physician assistants in the Mayo Clinic Health System
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
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: NPs & PAs referral discussions with a supervising physician
required consultations between NPs and PAs and their supervising physicians
|
Required discussion with physician prior to referral by a nurse practitioner or physician assistant
|
|
Other: NPs and PAs - no consultations with supervising physisians
NPs and PAs who are not required to discuss patient referrals
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Improved referrals from nurse practitioners and physician assistants to physicians as determined using a previously validated tool
Time Frame: 2 years
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Robert Lohr, MD, Mayo Clinic
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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
July 1, 2013
Primary Completion (Actual)
June 5, 2018
Study Completion (Actual)
June 5, 2018
Study Registration Dates
First Submitted
June 3, 2013
First Submitted That Met QC Criteria
June 10, 2013
First Posted (Estimate)
June 11, 2013
Study Record Updates
Last Update Posted (Actual)
October 3, 2019
Last Update Submitted That Met QC Criteria
October 1, 2019
Last Verified
October 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- 13-002913
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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