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Comparison · NCT04333199-3c567561

Timely Nudge vs Control: Enrollment - Timely Email (Combined Email Arms) vs. no Intervention

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. Timely Nudge vs Control: Enrollment - Timely Email (Combined Email Arms) vs. no Intervention. Trial comparisons, record NCT04333199-3c567561. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04333199-3c567561

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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 10.1080.0980.119wilson
Risk in group 20.03890.03070.0493wilson
Risk difference, group 1 minus group 20.06910.05470.0829newcombe hybrid score
Risk ratio, group 1 over group 22.782.153.59log
Odds ratio, group 1 over group 22.992.283.92log
Number needed to treat, for one more participant with the outcome on Timely Nudge than on Control14.512.118.3from the risk difference interval

Groups2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Timely NudgePatients are emailed about myGeisinger when they have a lab result ready to view.~Timely: Email3613,340OG001
Group 2ControlPatients do not receive an email651,669OG000

Outcome

Type
PRIMARY
Title
Enrollment - Timely Email (Combined Email Arms) vs. no Intervention
Description
Patient enrolled in myGeisinger (yes / no)
Time frame
1 week post-intervention
Population
Patients who were randomized and for whom there was a record in the EHR.

Source ClinicalTrials.gov

Trial

Title
Timely Nudge About Lab Results to Increase myGeisinger Uptake
NCT number
NCT04333199
Phases
NA
Conditions
Telehealth, Health Behavior
Interventions
Timely, Transparency, Foot-in-the-door
Lead sponsor
Geisinger Clinic
Results first posted
2021-05-03

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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