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Breast Cancer ScreeningNCT00224224

A Comparison of Primary Care and Traditional Internal Medicine Residents

An observational study of Breast Cancer Screening and Cervical Cancer Screening, run by Weill Medical College of Cornell University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this study is to identify objective differences between primary care and traditional medicine residents in clinical performance, continuity of care and utilization of resources. Read more about this study

Who is it for?
Ages 21 to 64 years
How many people
Not given
Where
1 siteUnited States
Study dates
Jan 1995to Jan 2005
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 to 64 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Patients who are followed as outpatients by a Cornell affiliated internist at the Cornell Internal Medicine Associates (CIMA).
  • Patients at New York Hospital who may or may not go on to be followed as outpatients at CIMA.

Who cannot join

  • Patients who elect not to participate in the study.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • New York Presbyterian Hospital-Weill Medical College

    New York, New York, 10065

Other trials in United States

About this study

The goal of this study is to identify objective differences between primary care and traditional medicine residents in clinical performance, continuity of care and utilization of resources. Specifically, this retrospective study will analyze the database collected by CLIMACS, the computer system at Cornell Internal Medicine Associates (CIMA). This system is used for clinical and administrative purposes; it manages and tracks patient's information and demographics, appointment booking, clinical diagnosis, prescriptions and medications, laboratory and radiology test, and consults. In our study, we will analyze a subset of the CLIMACS database from previous years.

Read the detailed description

Three areas will be examined:

  1. Clinical performance
  2. Continuity of care
  3. Utilization of resources

Clinical performance will be assessed using Health Plan Employer data and Information Set (HEDIS) performance standards. These standards were developed for the purposes of quality assessment, and in our study we will examine the following HEDIS standards:

  1. Breast Cancer Screening- the proportion of women between the ages of 52 and 64 who have had a mammogram within a two year period.
  2. Cervical Cancer Screening- the proportion of women between the ages of 21 and 64 who had a Pap test in the preceding 3 years.
  3. Cholesterol Screening- the proportion of patients ages 20 to 39 and 40-59 who have had their cholesterol tested at least once in the past five years.
  4. Asthma admission rate- the proportion of asthmatics admitted to the hospital for the care of asthma per year.
  5. Diabetic Standards-
  6. Admission for cellulitis/ 1000 diabetics per year.
  7. Admission for diabetes/ 1000 diabetics per year.
  8. Inpatient days per 100 diabetics per year.
  9. Prevalence of ischemic heart disease.
  10. Prevalence of severe renal disease.
  11. Diabetics with >2 hemoglobin A1C drawn per year.

Continuity of Care will be assessed by 3 different indicators:

  1. The proportion of visits that are made to the designated primary care provider of the number of visits made.
  2. The proportion of missed appointments of the total number of appointments.
  3. The proportion of walk in visits of the total number of appointments.

Resource utilization will be assessed by examining the following:

  1. Number of lab test per year per patient.
  2. Number of specialty consults per year per patient.
  3. Hospital admission rates per patient per year.
  4. Cost to medications. Confidentiality will be maintained throughout the study. In clinical practice access to CLIMACS is limited to the medical providers and administrators by individuals access codes. Furthermore, our study will remove specific identifiers to maintain the anonymity of both the patients and residents.
Keywords
Clinical performance, Continuity of care, Utilization of resources

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To identify the differences between primary care and traditional medicine residents in clinical performance, continuity of care and utilization of resources.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Sep 2005 (estimated)
  2. Study startJan 1995
  3. Study completionJan 2005

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Time perspective
Retrospective
IDs, dates and publications
ClinicalTrials.gov ID
NCT00224224
Sponsor's protocol ID
9510000400 (Formerly 1095-071)
Status last verified
Mar 2008
First submitted
20 Sep 2005
Last updated
3 Apr 2008
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Breast Cancer Screening and Cervical Cancer Screening, run by Weill Medical College of Cornell University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Apr 2008. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To identify the differences between primary care and traditional medicine residents in clinical performance, continuity of care and utilization of resources.. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Apr 2008.

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