Skip to main content
OpenTrials
Completed

NCT Number: NCT04927013

Connecting Families to Overcome Ovarian Cancer

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.

Completed

Looking for future studies?

Notify Me

Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Message-based Outreach Intervention for Survivors

Behavioral

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.

Standard Outreach for Survivors

Behavioral

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.

Message-based Outreach Intervention for Close Relatives

Behavioral

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.

Standard Outreach for Close Relatives

Behavioral

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 outcomes

  1. Number of Survivors Using Website Access Code

    Time frame: Up to 19 months

    Survivor reach is assessed as the number of the eligible survivors identified and contacted by GCR who used their unique login to access the study website.

  2. Number of Survivors Consenting to Participate in the Study

    Time frame: Up to 19 months

    Survivor reach is assessed as the number of the eligible survivors identified and contacted by GCR who used their unique login code to access the study website and consented to participate in the study while visiting the website.

  3. Number of Survivors Creating a Study Login

    Time frame: Up to 19 months

    Survivor reach is assessed as the number of the eligible survivors identified and contacted by GCR who access the study website, consented to participate in the study, and created their own personal study login on the website.

  4. Number of Relatives of Survivors Using the Website Access Code

    Time frame: Up to 19 months

    Close relative reach is assessed as the number of close relatives enumerated by survivors who used their unique login code to access the study website.

  5. Number of Relatives of Survivors Consenting to Participate in the Study

    Time frame: Up to 19 months

    Close relative reach is assessed as the number of close relatives enumerated by survivors who accessed the website and consented to participate in the study while they were using the website.

  6. Number of Relatives of Survivors Creating a Login

    Time frame: Up to 19 months

    Close relative reach is assessed as the number of close relatives enumerated by survivors who accessed the study website, gave consent to participate in the study, and created their own personal study login on the study website.

Secondary outcomes

  1. Relative Contact Option Selected by Survivors

    Time frame: Up to 19 months

    Cancer survivors in the Message-based Outreach Intervention arm who accessed the website were asked to enumerate close relatives and choose from a menu of options about how the survivor would prefer for their relatives to be contacted.

  2. Number of Survivors Requesting Telegenetic Counseling

    Time frame: Up to 19 months

    The request rate of cancer genetic services is assessed as the number of cancer survivors who requested telegenetic counseling on the website.

  3. Number of Survivors Completing Telegenetic Counseling

    Time frame: Up to 19 months

    Uptake of cancer genetic services is assessed as the number of survivors who completed telegenetic counseling.

  4. Number of Relatives Requesting Telegenetic Counseling

    Time frame: Up to 19 months

    The request rate of cancer genetic services is assessed as the number of close relatives who requested telegenetic counseling on the website.

  5. Number of Relatives Completing Telegenetic Counseling

    Time frame: Up to 19 months

    Uptake of cancer genetic services by relatives of survivors is assessed as the number of relatives enumerated who completed the Breast Cancer Genetics Referral Screening Tool (B-RST) screening and subsequently accessed genetic counseling.

  6. Time Visiting Website by Survivors

    Time frame: Up to 19 months

    The duration of time (in minutes) that survivors in the Message-based Outreach Intervention (MBI) study arm spent on the website was examined.

  7. Time Visiting Website by Relatives

    Time frame: Up to 19 months

    Among those in the intervention arm, the duration of time (in minutes) that relatives of survivors spend on the website was examined.

  8. Number of Return Visits to Website by Survivors

    Time frame: Up to 19 months

    The number of return visits to the website by survivors in the MBI study arm was examined.

  9. Number of Return Visits to Website by Relatives

    Time frame: Up to 19 months

    Among those in the intervention arm, the number of return visits to the website by relatives of survivors was examined.

  10. Number of Pages Viewed by Survivors

    Time frame: Up to 19 months

    The number of website page viewed by survivors in the MBI study arm was examined.

  11. Number of Pages Viewed by Relatives

    Time frame: Up to 19 months

    Among those in the intervention arm, the number of website pages viewed by relatives of survivors will be examined.

Sponsors and collaborators

Lead sponsor

Emory University

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

Testing a Low Cost Population- and Theory-Based Outreach Intervention to Engage Ovarian Cancer Survivors and Their Close Relatives to Consider Genetic Services

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Jun 15, 2021
Registry last updated
Oct 3, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.