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Decreasing Over Screening and Treatment of Cervical Precancers in Young Women

Primary Purpose

Cervical Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Provider Mobile Application (ProvAPP)
ProvAPP + Patient Educational Tool (Tab)
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Cervical Cancer focused on measuring Pap smear, Screening, Women, Human papillomavirus, Cervical precancer, Guideline adherence

Eligibility Criteria

21 Years - 29 Years (Adult)FemaleAccepts Healthy Volunteers

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

Sites / Locations

  • University of California, Los Angeles
  • University of California, San Francisco

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

No Intervention

No Intervention

Arm Label

Provider Mobile Application (ProvAPP)

ProvAPP + Patient Educational Tool (Tab)

ProvAPP Control Group

ProvAPP+Tab Control Group

Arm Description

Mobile phone application for providers.

Patient educational tool; plus the Mobile phone application for providers.

Clinics in this group are those NOT randomized - receiving no intervention. These clinics will be chosen at random for comparison using Family PACT claims data.

Clinics in this group are those NOT randomized - receiving no intervention. These clinics will be chosen at random for comparison using Family PACT claims data.

Outcomes

Primary Outcome Measures

Rate of Cervical Cancer Screening
Rate of women 21-29 years who received cervical cytology tests.

Secondary Outcome Measures

Rate of Colposcopy
Rate of women 21-29 years who receive colposcopy for cervical cancer screening over the total number of women 21-29 years.

Full Information

First Posted
October 14, 2014
Last Updated
September 23, 2019
Sponsor
University of California, San Francisco
Collaborators
Patient-Centered Outcomes Research Institute, Latinas Contra Cancer, National Cervical Cancer Coalition, California Department of Health Services, American College of Obstetricians and Gynecologists, American Society for Colposcopy and Cervical Pathology
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1. Study Identification

Unique Protocol Identification Number
NCT02270021
Brief Title
Decreasing Over Screening and Treatment of Cervical Precancers in Young Women
Official Title
Randomized Trial to Increase Adherence to Cervical Cancer Screening Guidelines for Young Women
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
July 24, 2014 (Actual)
Primary Completion Date
April 30, 2018 (Actual)
Study Completion Date
August 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
Patient-Centered Outcomes Research Institute, Latinas Contra Cancer, National Cervical Cancer Coalition, California Department of Health Services, American College of Obstetricians and Gynecologists, American Society for Colposcopy and Cervical Pathology

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

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 premature deliveries. Current national guidelines recommend that routine screening be performed at less-frequent intervals and that excisional cervical therapies are discouraged in young women. The objectives of this study are to examine physician- and patient-based interventions designed to decrease over screening and over treatment by increasing adherence to US guidelines for women under 30 years.
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 the American Society for Colposcopy and Cervical Pathology (ASCCP) guidelines for the management of abnormal cervical cancer screening tests and cancer precursors. Specifically, the interventions will focus on the newly recommended cervical cancer screening intervals and decreasing the number of colposcopy procedures and cervical procedures for abnormal cytology. This is a cluster randomized trial with individual clinics serving as the clusters. Clinics from the California Family PACT provider network who serve at least 200 female clients per year under 30 years of age will be randomized to one of two arms: 1) ASCCP mobile application (ProvAPP)-based intervention for providers, or 2) ProvAPP + Patient education Tool (Tab) intervention. These groups will be compared to a control comparison group of 28 clinics chosen using propensity score matching based on clinic characteristics such as county and private versus public from the Family PACT claims data. The ProvAPP intervention is for clinicians' mobile phones and will help them maneuver through current guidelines based on patient age and condition. An existing application from the ASCCP will be updated to include screening guidelines and to be more user-friendly. The patient-based Tab intervention will be a patient education tool accessible via URL on a tablet device at the time of check-in to assist in asking questions and evaluating treatment options. The tool will be developed with input from women age 21-29 as well as other stakeholders including Latinas Contra Cancer and the National Cervical Cancer Coalition. It is hypothesized that the ProvAPP+Tab approach will be most successful; all interventions will be more successful than no intervention. Family PACT serves predominantly uninsured women and 40% of clients are Latina. We plan to enroll 7 sites (ProvAPP) and 7 sites (ProvAPP+Tab) into the other intervention arm with an average of 2,800 women to 3,500 women aged 21-29 years per arm (14 sites) with a similar number of sites and women randomly chosen for the comparison arm (28 sites) resulting in a total of 39 sites and 8,400-10,500 women. We will use Family PACT claims data to examine, by age, the number of and average interval between cytology specimens, colposcopy examinations, and the number of excisional procedures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Cancer
Keywords
Pap smear, Screening, Women, Human papillomavirus, Cervical precancer, Guideline adherence

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
clinic sites were randomized not subjects
Masking
None (Open Label)
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Provider Mobile Application (ProvAPP)
Arm Type
Experimental
Arm Description
Mobile phone application for providers.
Arm Title
ProvAPP + Patient Educational Tool (Tab)
Arm Type
Experimental
Arm Description
Patient educational tool; plus the Mobile phone application for providers.
Arm Title
ProvAPP Control Group
Arm Type
No Intervention
Arm Description
Clinics in this group are those NOT randomized - receiving no intervention. These clinics will be chosen at random for comparison using Family PACT claims data.
Arm Title
ProvAPP+Tab Control Group
Arm Type
No Intervention
Arm Description
Clinics in this group are those NOT randomized - receiving no intervention. These clinics will be chosen at random for comparison using Family PACT claims data.
Intervention Type
Other
Intervention Name(s)
Provider Mobile Application (ProvAPP)
Intervention Description
Mobile phone application to maneuver clinicians through the cervical cancer screening and treatment guidelines based on patient age and condition.
Intervention Type
Other
Intervention Name(s)
ProvAPP + Patient Educational Tool (Tab)
Intervention Description
Patient Educational Tool (Tab): A patient educational tool (mobile tablet) will educate women on cervical cancer screening and treatment. Patients' self-assessment using a tablet at the time of clinic check-in will help them to understand current guidelines and their choices for treatment if they have abnormal cytology. It will allow them to assess the risks and benefits of screening intervals and of treatment choices. ProvAPP: Mobile phone application to maneuver clinicians through the cervical cancer screening and treatment guidelines based on patient age and condition.
Primary Outcome Measure Information:
Title
Rate of Cervical Cancer Screening
Description
Rate of women 21-29 years who received cervical cytology tests.
Time Frame
Change from baseline screening rate (3 months prior to intervention) to 15-18 months after start of intervention
Secondary Outcome Measure Information:
Title
Rate of Colposcopy
Description
Rate of women 21-29 years who receive colposcopy for cervical cancer screening over the total number of women 21-29 years.
Time Frame
Change from baseline colposcopy rate (3 months prior to intervention) to 15-18 months after start of intervention

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
29 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anna-Barbara Moscicki, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
33632649
Citation
Moscicki AB, Chang C, Vangala S, Zhou X, Elashoff DA, Dehlendorf C, Sawaya GF, Kuppermann M, Duron Y, Wyand FL, Navarro SK, Thiel de Bocanegra H. Effect of 2 Interventions on Cervical Cancer Screening Guideline Adherence. Am J Prev Med. 2021 May;60(5):666-673. doi: 10.1016/j.amepre.2020.11.015. Epub 2021 Feb 23.
Results Reference
derived

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Decreasing Over Screening and Treatment of Cervical Precancers in Young Women

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