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
About this trial
This is an interventional prevention trial for Hereditary Breast and Ovarian Cancer Syndrome
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.
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
NCT ID
NCT02956681
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
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
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Statewide Communication to Reach Diverse Low Income Women
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