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Comparison · NCT04927013-0c8616ab

Message-based Outreach Intervention (MBI) for Survivors vs Standard Outreach for Survivors: Number of Survivors Consenting to Participate in the Study

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Message-based Outreach Intervention (MBI) for Survivors vs Standard Outreach for Survivors: Number of Survivors Consenting to Participate in the Study. Trial comparisons, record NCT04927013-0c8616ab. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04927013-0c8616ab

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.8840.8230.927wilson
Risk in group 20.9110.8640.943wilson
Risk difference, group 1 minus group 2-0.0265-0.09610.0369newcombe hybrid score
Risk ratio, group 1 over group 20.9710.9031.04log
Odds ratio, group 1 over group 20.7480.3721.51log
Number needed to treat, for one fewer participant with the outcome on Message-based Outreach Intervention (MBI) for Survivors than on Standard Outreach for Survivors37.7from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Message-based Outreach Intervention (MBI) for SurvivorsCancer survivors randomized to receive a targeted letter with a unique website login code, access to the expanded website, free genetic counseling, and short message service (SMS) reminders.130147OG000
Group 2Standard Outreach for Survivors
Cancer survivors randomized to receive the standard outreach consisting of a standard letter with a unique website login code, access to a condensed version of the study website, and free genetic counseling.
184202OG001

Outcome

Type
PRIMARY
Title
Number of Survivors Consenting to Participate in the Study
Description
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.
Time frame
Up to 19 months
Population
The analysis population includes individuals who used their unique login code to access the study website.

Source ClinicalTrials.gov

Trial

Title
Connecting Families to Overcome Ovarian Cancer
NCT number
NCT04927013
Phases
NA
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
Lead sponsor
Emory University
Results first posted
2024-10-03

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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