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Statewide Communication to Reach Diverse Low Income Women

Primary Purpose

Hereditary Breast and Ovarian Cancer Syndrome

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Intervention Group
Delayed Intervention Group
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hereditary Breast and Ovarian Cancer Syndrome

Eligibility Criteria

25 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria

  • Residence within one of six local counties (for ease of access to our sites offering free genetic counseling and testing), age 25+, and English- or Spanish-speaking (the languages in which genetic counseling was conducted at risk program sites).

Exclusion Criteria

  • American Indian/Alaska Native and Native Hawaiian/Other Pacific Islander will not be included since very few call EWC.
  • Children (individuals under 25 years of age) will not be included in the study.
  • The rationale for this exclusion is that the research topic is not relevant to children.
  • The EWC does not target children, whose medical care is typically under the control of their parents or guardians.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Delayed Intervention Group

    Intervention Group

    Arm Description

    In this arm of the randomized delayed intervention control trial, participants randomized to delayed intervention control group were sent a brochure with information on hereditary breast and ovarian cancer and the phone number to call a cancer risk program for free genetic counseling.

    In this arm of the randomized delayed intervention control trial, those randomized to the intervention group were told that because of their family history, we were able to offer them a free genetic counseling appointment.

    Outcomes

    Primary Outcome Measures

    Receipt of Genetic Counseling During Intervention Period
    The primary outcome measure is receipt of genetic counseling within the two month intervention period.

    Secondary Outcome Measures

    Time to Counseling
    The study arms were compared with respect to time from randomization to counseling appointment using the log-rank test, and Kaplan-Meier curves were computed for each study arm.

    Full Information

    First Posted
    May 17, 2016
    Last Updated
    September 27, 2021
    Sponsor
    University of California, San Francisco
    Collaborators
    National Cancer Institute (NCI), Cancer Prevention Institute of California
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02956681
    Brief Title
    Statewide Communication to Reach Diverse Low Income Women
    Official Title
    Statewide Communication to Reach Diverse Low Income Women
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2021
    Overall Recruitment Status
    Completed
    Study Start Date
    October 2007 (undefined)
    Primary Completion Date
    September 2012 (Actual)
    Study Completion Date
    June 2013 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of California, San Francisco
    Collaborators
    National Cancer Institute (NCI), Cancer Prevention Institute of California

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Recruitment for prevention, and early detection among health disparities populations represents a major challenge in chronic disease control. This effect is magnified for individuals at high risk for conditions such as genetic breast cancer or chronic hepatitis. Costs are typically high, particularly given the common practice of developing a single outreach channel to address each disease or condition. In a randomized delayed intervention control trial, the investigators tested a strategy to identify low-income women at high risk for hereditary breast and ovarian cancer (HBOC) outside the clinical setting and refer them to free genetic counseling.
    Detailed Description
    This study addresses a disparity in services related to the rare but serious condition of HBOC. In a randomized delayed intervention control trial, the investigators were able to identify high-risk but predominantly unaffected women among callers seeking referrals to free cancer screening. The investigators compared an immediate offer of a genetic counseling appointment to information on hereditary breast and ovarian cancer sent by mail. Our study demonstrated that when a diverse population of low-income women calls a trusted information and referral source, it is possible to both engage them on a topic that is different from the purpose for their call and to recruit them for participation in research. Our intervention was designed to fit as seamlessly as possible with two end user organizations. Existing staff (Information Specialists) of the state's phone service administered a simple family history screener similar to their usual procedure for assessing eligibility for free mammography. Cancer Risk Program Genetic Counseling Assistants followed up with an outcall, just as they do normally in response to family history screeners filled out in the hospital's mammography clinic. Our results not only showed a significantly larger effect on use of genetic counseling with the call and appointment offer compared with a mailed brochure, it was clear from calls made to women in both arms after the intervention period that calling is not only effective but essential to encourage use of genetic counseling in this population. The number of women counseled in the intervention group was initially much higher than the control group, and additional intervention group members obtained counseling when called again after the two month intervention period. The addition of genetic counseling by phone enabled a substantial number of women to obtain counseling who would not have done so otherwise. Our study demonstrated that, for the complex and highly personal issue of HBOC, multiple attempts over a period of months are needed and justified.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Hereditary Breast and Ovarian Cancer Syndrome

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    88 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Delayed Intervention Group
    Arm Type
    Active Comparator
    Arm Description
    In this arm of the randomized delayed intervention control trial, participants randomized to delayed intervention control group were sent a brochure with information on hereditary breast and ovarian cancer and the phone number to call a cancer risk program for free genetic counseling.
    Arm Title
    Intervention Group
    Arm Type
    Active Comparator
    Arm Description
    In this arm of the randomized delayed intervention control trial, those randomized to the intervention group were told that because of their family history, we were able to offer them a free genetic counseling appointment.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Intervention Group
    Intervention Description
    Callers to California's toll-free breast/cervical screening phone service were screened for family history. Callers identified as high risk will be told that a genetic counselor will call them back to offer them a free genetic counseling appointment and that a brochure will be sent. A UCSF/SFGH genetic counseling assistant will call them back within a few days to offer them a free genetic counseling appointment at SFGH.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Delayed Intervention Group
    Intervention Description
    This is a randomized delayed intervention control trial in which eligible callers to California's toll-free breast/cervical screening phone service were screened for family history. Callers identified as high risk will be told that they are eligible to speak to a genetic counselor who is available at no charge at SFGH and that they will be sent a brochure with information on where to call.
    Primary Outcome Measure Information:
    Title
    Receipt of Genetic Counseling During Intervention Period
    Description
    The primary outcome measure is receipt of genetic counseling within the two month intervention period.
    Time Frame
    Up to three years
    Secondary Outcome Measure Information:
    Title
    Time to Counseling
    Description
    The study arms were compared with respect to time from randomization to counseling appointment using the log-rank test, and Kaplan-Meier curves were computed for each study arm.
    Time Frame
    Up to three years

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    25 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria Residence within one of six local counties (for ease of access to our sites offering free genetic counseling and testing), age 25+, and English- or Spanish-speaking (the languages in which genetic counseling was conducted at risk program sites). Exclusion Criteria American Indian/Alaska Native and Native Hawaiian/Other Pacific Islander will not be included since very few call EWC. Children (individuals under 25 years of age) will not be included in the study. The rationale for this exclusion is that the research topic is not relevant to children. The EWC does not target children, whose medical care is typically under the control of their parents or guardians.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Rena J Pasick, DrPH
    Organizational Affiliation
    University of California, San Francisco
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Statewide Communication to Reach Diverse Low Income Women

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