Status:
COMPLETED
Decreasing Over Screening and Treatment of Cervical Precancers in Young Women
Lead Sponsor:
University of California, San Francisco
Collaborating Sponsors:
Patient-Centered Outcomes Research Institute
Latinas Contra Cancer
Conditions:
Cervical Cancer
Eligibility:
FEMALE
21-29 years
Phase:
NA
Brief Summary
The goal of this study is to prevent over screening and over treatment of young women for cervical precancers, which can result in psychological distress and has been associated with future risk of pr...
Detailed Description
In this study, we compare two different intervention arms that are designed to prevent over screening and over treatment by increasing adherence to the new US cervical cancer screening guidelines and ...
Eligibility Criteria
Inclusion
- Inclusion Criteria - Patients:
- English or Spanish speaking
- Women
- Age 21-29 years
- History of one or more of the following: abnormal Pap smear, normal Pap smear, no Pap smear, cervical cancer
- Exclusion Criteria - Patients:
- Language other than English or Spanish
- Male
- Younger than 21 or older than 29
- Inclusion Criteria - Clinics:
- Family PACT provider
- Not a Planned Parenthood affiliate
- Located in one of ten identified Southern California study counties
- Sends cytology/histology specimens to Quest Diagnostics West Hills
- Clinical care visits occurred to at least 200 women age 21-29 years in fiscal year 2011/2012
- Has a calculated average cytology interval of less than 30 months (based on last three years)
- Exclusion Criteria - Clinics:
- Not a Family PACT provider
- Planned Parenthood affiliate
- Not located in one of ten identified Southern California study counties
- Sends cytology/histology specimens to a lab other than Quest Diagnostics West Hills
- Clinical care visit occurred to less than 200 women age 21-29
- Has a calculated average cytology interval of more than 30 months
Exclusion
Key Trial Info
Start Date :
July 24 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 30 2019
Estimated Enrollment :
42 Patients enrolled
Trial Details
Trial ID
NCT02270021
Start Date
July 24 2014
End Date
August 30 2019
Last Update
September 25 2019
Active Locations (2)
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1
University of California, Los Angeles
Los Angeles, California, United States, 90095
2
University of California, San Francisco
San Francisco, California, United States, 94143