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Study Summary
No. 2005-0543:.......Gynecology......Judith A. Smith......Gynecologic Oncology
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Study Summary Title
Study Summary
Number:
2005-0543
Study Title:Evaluation of the Educational Interventions on Medical Team Compliance with NCCN Myeloid Growth Factor Guidelines
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Physician New Patient Referral
Name:Judith A. SmithPatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:Gynecologic OncologyReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-500-6408
Contact us about clinical trials
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General Information
Disease Group:GynecologySupported By:N/A
Phase of Study:N/AReturn
Visit:
None
Treatment
Agents:
NoneHome Care:None
Treatment Loc:Only at MDACC
Estimated
Length of Stay
in Houston:
Not Applicable
Description/
Intervention:
Unavailable
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Study Objectives / Outcomes
PRIMARY OBJECTIVES:
1.1 Determine the current practice patterns use of colony stimulating growth factors during chemotherapy in the UT MD Anderson Cancer Center (UTMDACC) Gynecology Oncology Center.

1.2 Establish if evidence-based educational interventions supported by a practice guideline influences a change in clinical practice in the UT MD Anderson Cancer Center (UTMDACC) Gynecology Oncology Center.

A change in clinical practice will be demonstrated by an increase in the percent of patients treated by standards set in the NCCN Myeloid Growth Factor Guideline, including the appropriate setting (primary or secondary prophylaxis), use level (including appropriate use at febrile neutropenia (FN) risk levels above 20% and inappropriate use at FN risk levels below 10%), and dosing based on regimen and patient risk factors.

SECONDARY OBJECTIVES:
1.3 Compare and contrast the incidence of treatment delays and patient satisfaction with chemotherapy experience before and after the evidence-based educational interventions..

1.4 Compare and contrast the incidence of chemotherapy-induced neutropenia (CIN); chemotherapy-induced febrile neutropenia (FN) and FN related hospitalizations (FNH) along with the frequency of these complications by cycle with chemotherapy regimens commonly used for the treatment of gynecologic malignancies before and after the evidence-based educational interventions.

1.5 Compare and contrast the hospitalization and anti-infective utilization rates associated with CIN, FN, FNH before and after the evidence-based educational interventions.

1.6 Identify the patient demographic characteristics and risk factors associated with CIN, FN, FNH.
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Study Status Information
Study Activation / Registration Date:07/30/2007
IRB Review and Approval Date:07/30/2007
Study Type:Observational
Recruitment Status:Terminated
Projected Accrual:N/A
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Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:1) Patient receiving chemotherapy for the treatment of a gynecologic malignancy at UTMDACC Gynecology Oncology Center.

2) All healthcare providers including Attending physicians, fellows, and nurses that practice/work at UTMDACC Gynecology Oncology Center.

Exclusion Criteria:1) Patients receiving investigational agents or on research studies for the treatment of a gynecologic malignancy at UTMDACC Gynecology Oncology Center.

2) Patients with an altered mental status or inability to consent to participate in the protocol. Patients unable to read or write the English or Spanish language because language limitations to complete study assessment tools (FACT-N).

3) Visiting residents and trainees that will not be present for the duration of the study (at least 1 year).

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Links
Registration Number: Not Applicable Clinical Trial

Other Links:
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Results


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