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Comparison · NCT02646423-d8912bd7

Prior CD Decision App (PCDDA) vs Usual Care - No App: Number of Participants Who Underwent Vaginal Birth After Cesarean (VBAC)

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. Prior CD Decision App (PCDDA) vs Usual Care - No App: Number of Participants Who Underwent Vaginal Birth After Cesarean (VBAC). Trial comparisons, record NCT02646423-d8912bd7. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02646423-d8912bd7

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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 10.3180.2850.352wilson
Risk in group 20.3180.2860.353wilson
Risk difference, group 1 minus group 2-0.000562-0.04830.0472newcombe hybrid score
Risk ratio, group 1 over group 20.9980.8591.16log
Odds ratio, group 1 over group 20.9970.81.24log
Number needed to treat, for one fewer participant with the outcome on Prior CD Decision App (PCDDA) than on Usual Care - No App1,780from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: usual care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Prior CD Decision App (PCDDA)
Women who are randomized to PCDDA will be provided access to a tablet which they can use to view the Prior CD Decision App at their own pace. The research assistant will print a summary of the participant's predicted likelihood of a vaginal delivery (VBAC) if she undergoes a trial of labor (TOLAC), as well as her answers to the values clarification exercises, that she can review and share with whomever she chooses, including her provider.
231727OG000
Group 2Usual Care - No AppWomen randomized to the Usual Care - No App group will simply continue with usual care.233732OG001

Outcome

Type
SECONDARY
Title
Number of Participants Who Underwent Vaginal Birth After Cesarean (VBAC)
Description
Number of participants who underwent vaginal birth after cesarean (VBAC), as noted in the medical record.
Time frame
0 to 8 weeks after delivery
Population
Prior CD Decision App (PCDDA): no data available for N=8 participants who delivered at outside institution and no chart or outside questionnaire obtained.~Usual Care - No App: no data available for N=3 participants who delivered at outside institution and no chart or outside questionnaire obtained.

Source ClinicalTrials.gov

Trial

Title
Effect of a Patient-Centered Decision App on TOLAC
NCT number
NCT02646423
Phases
NA
Conditions
Pregnancy, Repeat Cesarean Section, Vaginal Births After Cesarean
Interventions
Prior CD Decision App
Lead sponsor
University of California, San Francisco
Results first posted
2021-02-02

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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