Registered outcomes17

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

1 to 17 of 17

List	Outcome	Time frame	Description
Primary	Number of Survivors Using Website Access Code	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.
Primary	Number of Survivors Consenting to Participate in the Study	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.
Primary	Number of Survivors Creating a Study Login	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.
Primary	Number of Relatives of Survivors Using the Website Access Code	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.
Primary	Number of Relatives of Survivors Consenting to Participate in the Study	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.
Primary	Number of Relatives of Survivors Creating a Login	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	Relative Contact Option Selected by Survivors	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.
Secondary	Number of Survivors Requesting Telegenetic Counseling	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.
Secondary	Number of Survivors Completing Telegenetic Counseling	Up to 19 months	Uptake of cancer genetic services is assessed as the number of survivors who completed telegenetic counseling.
Secondary	Number of Relatives Requesting Telegenetic Counseling	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.
Secondary	Number of Relatives Completing Telegenetic Counseling	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.
Secondary	Time Visiting Website by Survivors	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.
Secondary	Time Visiting Website by Relatives	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.
Secondary	Number of Return Visits to Website by Survivors	Up to 19 months	The number of return visits to the website by survivors in the MBI study arm was examined.
Secondary	Number of Return Visits to Website by Relatives	Up to 19 months	Among those in the intervention arm, the number of return visits to the website by relatives of survivors was examined.
Secondary	Number of Pages Viewed by Survivors	Up to 19 months	The number of website page viewed by survivors in the MBI study arm was examined.
Secondary	Number of Pages Viewed by Relatives	Up to 19 months	Among those in the intervention arm, the number of website pages viewed by relatives of survivors will be examined.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
ClinicalTrials.govNo license stated
NIH RePORTER's clinical studies and project filesPublic domain

Each source's terms

ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
ClinicalTrials.govnone stated
NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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