Trial · NCT04927013
Connecting Families to Overcome Ovarian Cancer
NCT04927013, Not applicable, Completed, Emory University; results first posted 2024-10-03
3 sourcestrials-2026-11-12-0.5.0
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ConductScience Library. Connecting Families to Overcome Ovarian Cancer. Trials, record NCT04927013. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04927013
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Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Connecting Families to Overcome Ovarian Cancer
- NCT number
- NCT04927013
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 2,331 participants, actual
- Lead sponsor
- Emory University
- Conditions
- Ovarian Cancer
- Interventions
- Message-based Outreach Intervention for Survivors, Standard Outreach for Survivors, Message-based Outreach Intervention for Close Relatives, Standard Outreach for Close Relatives
- First posted
- 2021-06-15
- Last updated
- 2024-10-03
- Results first posted
- 2024-10-03
Source ClinicalTrials.gov
Registered outcomes17
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| 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. |
1 to 10 of 17Source ClinicalTrials.gov
See all 17 registered outcomesOutcomes17
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Survivors Using Website Access Code | Up to 19 months | Participants | COUNT_OF_PARTICIPANTS | |
| PRIMARY | Number of Survivors Consenting to Participate in the Study | Up to 19 months | The analysis population includes individuals who used their unique login code to access the study website. | Participants | COUNT_OF_PARTICIPANTS |
| PRIMARY | Number of Survivors Creating a Study Login | Up to 19 months | The analysis population includes individuals who gave consent to participate in the study. | Participants | COUNT_OF_PARTICIPANTS |
| PRIMARY | Number of Relatives of Survivors Using the Website Access Code | Up to 19 months | The analysis population includes close relatives of cancer survivors who were identified by the survivors to be contacted and offered the opportunity to participate in the study. | Participants | COUNT_OF_PARTICIPANTS |
| PRIMARY | Number of Relatives of Survivors Consenting to Participate in the Study | Up to 19 months | The analysis population includes close relatives who accessed the study website. | Participants | COUNT_OF_PARTICIPANTS |
| PRIMARY | Number of Relatives of Survivors Creating a Login | Up to 19 months | This analysis population includes close relatives who gave consent to participate in the study. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Relative Contact Option Selected by Survivors | Up to 19 months | This analysis population includes cancer survivors who accessed the website and selected a contact method for the close relatives that they provided contact information for. Survivors could identify more than one close relative and some did not identify any relatives. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Survivors Requesting Telegenetic Counseling | Up to 19 months | This analysis includes participants who accessed the study website. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Survivors Completing Telegenetic Counseling | Up to 19 months | This analysis includes participants who requested telegenetic counseling on the website. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Relatives Requesting Telegenetic Counseling | Up to 19 months | This analysis population includes close relatives who gave consent to participate in the study. | Participants | COUNT_OF_PARTICIPANTS |
1 to 10 of 17Source ClinicalTrials.gov
See all 17 outcomesResults by group29
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Survivors Using Website Access Code | Message-based Outreach Intervention (MBI) for Survivors | 147 | Participants | ||
| Number of Survivors Using Website Access Code | Standard Outreach for Survivors | 202 | Participants | ||
| Number of Survivors Consenting to Participate in the Study | Message-based Outreach Intervention (MBI) for Survivors | 130 | Participants | ||
| Number of Survivors Consenting to Participate in the Study | Standard Outreach for Survivors | 184 | Participants | ||
| Number of Survivors Creating a Study Login | Message-based Outreach Intervention (MBI) for Survivors | 126 | Participants | ||
| Number of Survivors Creating a Study Login | Standard Outreach for Survivors | 174 | Participants | ||
| Number of Relatives of Survivors Using the Website Access Code | Message-based Outreach Intervention for Close Relatives | 20 | Participants | ||
| Number of Relatives of Survivors Using the Website Access Code | Standard Outreach for Close Relatives | 1 | Participants | ||
| Number of Relatives of Survivors Consenting to Participate in the Study | Message-based Outreach Intervention for Close Relatives | 19 | Participants | ||
| Number of Relatives of Survivors Consenting to Participate in the Study | Standard Outreach for Close Relatives | 1 | Participants |
1 to 10 of 29Source ClinicalTrials.gov
See all 29 results by groupParticipant flow12
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Message-based Outreach Intervention (MBI) for Survivors | 969 | |
| Overall Study | STARTED | Standard Outreach for Survivors | 969 | |
| Overall Study | STARTED | Message-based Outreach Intervention for Close Relatives | 152 | |
| Overall Study | STARTED | Standard Outreach for Close Relatives | 241 | |
| Overall Study | COMPLETED | Message-based Outreach Intervention (MBI) for Survivors | 130 | |
| Overall Study | COMPLETED | Standard Outreach for Survivors | 184 | |
| Overall Study | COMPLETED | Message-based Outreach Intervention for Close Relatives | 19 | |
| Overall Study | COMPLETED | Standard Outreach for Close Relatives | 1 | |
| Overall Study | NOT COMPLETED | Message-based Outreach Intervention (MBI) for Survivors | 839 | |
| Overall Study | NOT COMPLETED | Standard Outreach for Survivors | 785 |
1 to 10 of 12Source ClinicalTrials.gov
See all 12 participant flowAdverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals12
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Message-based Outreach Intervention (MBI) for Survivors | 0 | 969 |
| Total, all-cause mortality | Standard Outreach for Survivors | 0 | 969 |
| Total, all-cause mortality | Message-based Outreach Intervention for Close Relatives | 0 | 152 |
| Total, all-cause mortality | Standard Outreach for Close Relatives | 0 | 241 |
| Total, other adverse events | Message-based Outreach Intervention (MBI) for Survivors | 0 | 969 |
| Total, other adverse events | Standard Outreach for Survivors | 0 | 969 |
| Total, other adverse events | Message-based Outreach Intervention for Close Relatives | 0 | 152 |
| Total, other adverse events | Standard Outreach for Close Relatives | 0 | 241 |
| Total, serious adverse events | Message-based Outreach Intervention (MBI) for Survivors | 0 | 969 |
| Total, serious adverse events | Standard Outreach for Survivors | 0 | 969 |
1 to 10 of 12Source ClinicalTrials.gov
See all 12 adverse event totalsPapers2
The papers the trial lists on ClinicalTrials.gov.
Grants1
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years |
|---|---|---|---|---|---|
| U01CA240581 | Testing a Low Cost Population- and Theory-Based Outreach Intervention to Engage Ovarian Cancer Survivors and their Close Relatives to Consider Genetic Services | GUAN, YUE | EMORY UNIVERSITY | NATIONAL CANCER INSTITUTE | 2020 to 2023 |
Source NIH RePORTER
Trial comparisons9
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Message-based Outreach Intervention (MBI) for Survivors vs Standard Outreach for Survivors: Number of Survivors Consenting to Participate in the Study | Trial comparisons |
| Message-based Outreach Intervention (MBI) for Survivors vs Standard Outreach for Survivors: Number of Survivors Creating a Study Login | Trial comparisons |
| Message-based Outreach Intervention for Close Relatives vs Standard Outreach for Close Relatives: Number of Relatives of Survivors Using the Website Access Code | Trial comparisons |
| Message-based Outreach Intervention for Close Relatives vs Standard Outreach for Close Relatives: Number of Relatives of Survivors Consenting to Participate in the Study | Trial comparisons |
| Message-based Outreach Intervention (MBI) for Survivors vs Standard Outreach for Survivors: Number of Survivors Completing Telegenetic Counseling | Trial comparisons |
| Message-based Outreach Intervention for Close Relatives vs Standard Outreach for Close Relatives: Number of Relatives Requesting Telegenetic Counseling | Trial comparisons |
| Message-based Outreach Intervention (MBI) for Survivors vs Standard Outreach for Survivors: Number of Survivors Using Website Access Code | Trial comparisons |
| Message-based Outreach Intervention for Close Relatives vs Standard Outreach for Close Relatives: Number of Relatives of Survivors Creating a Login | Trial comparisons |
| Message-based Outreach Intervention (MBI) for Survivors vs Standard Outreach for Survivors: Number of Survivors Requesting Telegenetic Counseling | Trial comparisons |
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
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.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04927013
GET https://conductscience.org/api/trials/v1/NCT04927013/results?page=2