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Connecting Families to Overcome Ovarian Cancer

Primary Purpose

Ovarian Cancer

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Message-based Outreach Intervention for Survivors
Standard Outreach for Survivors
Message-based Outreach Intervention for Close Relatives
Standard Outreach for Close Relatives
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Ovarian Cancer focused on measuring Genetic counseling, Risk assessment, Family communication, Genetic risk communication

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria for Survivors:

  • in the Georgia Cancer Registry (GSR)
  • diagnosed with ovarian, fallopian tube, or peritoneal cancers
  • lived in Georgia at the time of diagnosis
  • not deceased per the registry's records
  • have a mailing address in GSR records

Inclusion Criteria for Close Relatives:

  • 25 years or older
  • able to access the internet
  • a 1st or 2nd degree relative of the survivor
  • able to read English
  • non-incarcerated or institutionalized

Exclusion Criteria:

  • none

Sites / Locations

  • Emory UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

Arm Label

Message-based Outreach Intervention (MBI) for Survivors

Standard Outreach for Survivors

Message-based Outreach Intervention for Close Relatives

Standard Outreach for Close Relatives

Arm Description

Cancer survivors randomized to receive a targeted letter with a unique website log in, access to the expanded website, free genetic counseling, and short message service (SMS) reminders.

Cancer survivors randomized to receive the standard outreach consisting of a standard letter with website access, access to a condensed version of the study website, and free genetic counseling.

Close relatives of cancer survivors who were randomized to receive the message-based outreach. Close relatives will have access to the expanded version of the study website and free genetic counseling.

Close relatives of cancer survivors who were randomized to receive the standard outreach. Close relatives will have access to a condensed version of the study website and free genetic counseling.

Outcomes

Primary Outcome Measures

Proportion of Survivors Accessing the Website
Survivor reach is assessed as the proportion of the eligible survivors identified and contacted by GCR who log in to the website.
Proportion of Relatives of Survivors Accessing the Website
Close relative reach is assessed as the proportion of close relatives enumerated by survivors who log in to the website.
Proportion of Survivors Completing Telegenetic Counseling
Uptake of cancer genetic services will be assessed as the proportion of untested survivors who complete telegenetic counseling.
Proportion of Relatives Completing Telegenetic Counseling
Uptake of cancer genetic services by relatives of survivors will be assessed as the proportion of relatives enumerated who complete the Breast Cancer Genetics Referral Screening Tool (B-RST) screening and subsequently access genetic counseling.

Secondary Outcome Measures

Time Visiting Website by Survivors
Among those in the intervention arm, the duration of time (in minutes) that survivors spend on the website will be examined.
Time Visiting Website by Relatives
Among those in the intervention arm, the duration of time (in minutes) that relatives of survivors spend on the website will be examined.
Number of Return Visits to Website by Survivors
Among those in the intervention arm, the number of return visits to the website by survivors will be examined.
Number of Return Visits to Website by Relatives
Among those in the intervention arm, the number of return visits to the website by relatives of survivors will be examined.
Number of Pages Viewed by Survivors
Among those in the intervention arm, the number of website pages viewed by survivors will be examined.
Number of Pages Viewed by Relatives
Among those in the intervention arm, the number of website pages viewed by relatives of survivors will be examined.
Proportion Selecting Contact Options
The proportion of survivors in the intervention arm who select different relative contact options will be examined.

Full Information

First Posted
June 14, 2021
Last Updated
October 18, 2022
Sponsor
Emory University
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT04927013
Brief Title
Connecting Families to Overcome Ovarian Cancer
Official Title
Testing a Low Cost Population- and Theory-Based Outreach Intervention to Engage Ovarian Cancer Survivors and Their Close Relatives to Consider Genetic Services
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 24, 2021 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
April 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University
Collaborators
National Cancer Institute (NCI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study tests a multi-component, low cost, message-based communication outreach intervention to engage ovarian cancer survivors and their at-risk relatives in considering cancer genetic services. The intervention includes foot-in-the-door techniques, tailored/targeted print, website support, and short messages to expand reach of prevention messages.
Detailed Description
The majority of women at greatest risk for ovarian cancer due to hereditary factors are unlikely to be aware of their elevated risk and available prevention options. Thus, most at-risk women are diagnosed when their ovarian cancer is advanced and treatment options are limited. Additionally, efforts to broaden awareness of genetic risk among at risk families has been very limited. State cancer registries' offer a potentially low cost platform for providing resources to ovarian cancer survivors and their close relatives. In partnership with the Georgia Cancer Registry (GCR), the researchers are testing two different communication approaches to provide inherited risk information and free genetic counseling to ovarian cancer survivors and their close blood relatives. Participants will be assigned at random to visit one of two websites; those assigned to the "message-based" site will be offered assistance from the study team to contact close relatives and reminder messages and those viewing the other site will not. The researchers are testing which of the two approaches is most effective as indicated by: the number of survivors who visit the website; the number of close relatives who visit the website and the number of survivors and relatives who complete a genetic counseling session. The researchers hypothesize that the message-based approach will result in greater reach and uptake of genetic services than a standard approach. The two outreach websites with content for both survivors and close relatives will be the hub in the wheel of intervention activity. In turn, the researchers will encourage access to the website using other communication channels as the spokes. The GCR will make initial contact with ovarian cancer survivors. The Registry will: 1) mail a packet of information about the study to identified survivors, and 2) make follow-up phone calls and send reminder postcards to encourage study participation. Survivors can then visit the assigned website and click a button indicating they agree to participate. Survivors assigned to the message-based intervention will receive additional short text messages encouraging them to contact relatives and seek genetic counseling. Relatives in this message-based group who choose to participate will also receive these short messages if they choose to provide contact information. Free genetic counseling is being offered to participants in both study arms. The researchers are collaborating with Emory's Genetic Counseling Training program under the supervision of two certified genetic counselors. This study uses tele-medicine approaches to ensure access of survivors and relatives living in Georgia and elsewhere. The results of the study could guide the development of outreach strategies for Georgia and other states to offer sustainable services to expand the reach of genetic services for ovarian and other heritable cancers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ovarian Cancer
Keywords
Genetic counseling, Risk assessment, Family communication, Genetic risk communication

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
1240 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Message-based Outreach Intervention (MBI) for Survivors
Arm Type
Experimental
Arm Description
Cancer survivors randomized to receive a targeted letter with a unique website log in, access to the expanded website, free genetic counseling, and short message service (SMS) reminders.
Arm Title
Standard Outreach for Survivors
Arm Type
Active Comparator
Arm Description
Cancer survivors randomized to receive the standard outreach consisting of a standard letter with website access, access to a condensed version of the study website, and free genetic counseling.
Arm Title
Message-based Outreach Intervention for Close Relatives
Arm Type
Experimental
Arm Description
Close relatives of cancer survivors who were randomized to receive the message-based outreach. Close relatives will have access to the expanded version of the study website and free genetic counseling.
Arm Title
Standard Outreach for Close Relatives
Arm Type
Active Comparator
Arm Description
Close relatives of cancer survivors who were randomized to receive the standard outreach. Close relatives will have access to a condensed version of the study website and free genetic counseling.
Intervention Type
Behavioral
Intervention Name(s)
Message-based Outreach Intervention for Survivors
Intervention Description
The Georgia Cancer Registry will mail the initial recruitment containing messages intended to persuade the survivor to visit the study website as well as a unique login to access the website. In addition to the components of the standard website, an expanded website for the Message-based group will include Guidance for Talking with Close Relatives about Their Cancer Risk, and the request to enumerate each close relative and choose from a menu of options about how the survivor would prefer for their relatives to be contacted. Survivors also can select the option that they prefer a relative not be contacted. In this case, no invitation letter will be generated for these relatives. Survivors who provide mobile phone numbers will receive two SMS thanking them for accessing the website, and encouraging them to revisit the website to review information and contact relatives. The messages will occur at 3-week intervals over a 6-week time period.
Intervention Type
Behavioral
Intervention Name(s)
Standard Outreach for Survivors
Intervention Description
The Georgia Cancer Registry will mail survivors an introductory letter modeled on the Registry's general outreach letters that will include log-in information. Survivors will have access to a condensed version of the website that includes Information about Ovarian Cancer, Information about Who in Your Family is at Increased Risk, and the offer of Free Genetic Counseling with the option to schedule an appointment.
Intervention Type
Behavioral
Intervention Name(s)
Message-based Outreach Intervention for Close Relatives
Intervention Description
Relatives will receive a unique website login linked to the survivor that enables access to the website. The website content will be identical to the survivor content with the exception of the addition of the Breast Cancer Genetics Referral Screening Tool (B-RST) risk assessment tool. This brief risk assessment is a validated screening tools that is clinically useful for estimating the probability of breast cancer (BRCA1/2) gene mutation and identifying women for referral to genetic counseling. Although all 1st or 2nd degree relatives of ovarian cancer survivors will screen positive on B-RST, asking relatives to complete the screener aims to raise their awareness of the factors that contribute to hereditary risk of ovarian cancer and will reinforce the salience of seeking genetic counseling. Additionally, relatives for who provide cell phone numbers will receive 3 SMS reminders over 9 weeks.
Intervention Type
Behavioral
Intervention Name(s)
Standard Outreach for Close Relatives
Intervention Description
The invitation letter shared by the survivor will provide a unique login code for each relative to visit the standard website with sections specifically for relatives that include information about genetic risk, the value of completing an online short validated risk screener, and the offer of free genetic counseling with the option to schedule an appointment.
Primary Outcome Measure Information:
Title
Proportion of Survivors Accessing the Website
Description
Survivor reach is assessed as the proportion of the eligible survivors identified and contacted by GCR who log in to the website.
Time Frame
Up to 31 months
Title
Proportion of Relatives of Survivors Accessing the Website
Description
Close relative reach is assessed as the proportion of close relatives enumerated by survivors who log in to the website.
Time Frame
Up to 31 months
Title
Proportion of Survivors Completing Telegenetic Counseling
Description
Uptake of cancer genetic services will be assessed as the proportion of untested survivors who complete telegenetic counseling.
Time Frame
Up to 31 months
Title
Proportion of Relatives Completing Telegenetic Counseling
Description
Uptake of cancer genetic services by relatives of survivors will be assessed as the proportion of relatives enumerated who complete the Breast Cancer Genetics Referral Screening Tool (B-RST) screening and subsequently access genetic counseling.
Time Frame
Up to 31 months
Secondary Outcome Measure Information:
Title
Time Visiting Website by Survivors
Description
Among those in the intervention arm, the duration of time (in minutes) that survivors spend on the website will be examined.
Time Frame
Up to 31 months
Title
Time Visiting Website by Relatives
Description
Among those in the intervention arm, the duration of time (in minutes) that relatives of survivors spend on the website will be examined.
Time Frame
Up to 31 months
Title
Number of Return Visits to Website by Survivors
Description
Among those in the intervention arm, the number of return visits to the website by survivors will be examined.
Time Frame
Up to 31 months
Title
Number of Return Visits to Website by Relatives
Description
Among those in the intervention arm, the number of return visits to the website by relatives of survivors will be examined.
Time Frame
Up to 31 months
Title
Number of Pages Viewed by Survivors
Description
Among those in the intervention arm, the number of website pages viewed by survivors will be examined.
Time Frame
Up to 31 months
Title
Number of Pages Viewed by Relatives
Description
Among those in the intervention arm, the number of website pages viewed by relatives of survivors will be examined.
Time Frame
Up to 31 months
Title
Proportion Selecting Contact Options
Description
The proportion of survivors in the intervention arm who select different relative contact options will be examined.
Time Frame
Up to 31 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria for Survivors: in the Georgia Cancer Registry (GSR) diagnosed with ovarian, fallopian tube, or peritoneal cancers lived in Georgia at the time of diagnosis not deceased per the registry's records have a mailing address in GSR records Inclusion Criteria for Close Relatives: 25 years or older able to access the internet a 1st or 2nd degree relative of the survivor able to read English non-incarcerated or institutionalized Exclusion Criteria: none
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Colleen McBride, PhD
Phone
404-727-8226
Email
colleen.marie.mcbride@emory.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Yue Guan, PhD, MS
Email
yue.guan@emory.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Colleen McBride, PhD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All of the individual participant data collected during the trial will be available for sharing, after de-identification.
IPD Sharing Time Frame
Data will be available for sharing immediately following the publication and release of the key manuscripts tied to the primary aims of this study, and ending approximately 18 months after funding ends.
IPD Sharing Access Criteria
Individual participant data will be available for sharing with researchers who provide a methodologically sound proposal, in order to achieve the aims stated in the approved proposal. Proposals should be directed to Dr. Colleen McBride at colleen.marie.mcbride@emory.edu. To gain access, data requestors will need to sign a data access agreement.

Learn more about this trial

Connecting Families to Overcome Ovarian Cancer

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