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Comparison · NCT02646423-dffd7fe3

Prior CD Decision App (PCDDA) vs Usual Care - No App: Neonatal Respiratory Morbidity

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: Neonatal Respiratory Morbidity. Trial comparisons, record NCT02646423-dffd7fe3. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02646423-dffd7fe3

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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 10.09320.0740.117wilson
Risk in group 20.09430.07510.118wilson
Risk difference, group 1 minus group 2-0.00113-0.03150.0292newcombe hybrid score
Risk ratio, group 1 over group 20.9880.7171.36log
Odds ratio, group 1 over group 20.9870.6921.41log
Number needed to treat, for one fewer participant with the outcome on Prior CD Decision App (PCDDA) than on Usual Care - No App886from 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.
67719OG000
Group 2Usual Care - No AppWomen randomized to the Usual Care - No App group will simply continue with usual care.68721OG001

Outcome

Type
SECONDARY
Title
Neonatal Respiratory Morbidity
Description
Respiratory morbidity requiring CPAP or intubation, as noted in the medical record for her delivery.
Time frame
Collected 0 to 8 weeks after delivery.
Population
PCDDA: 15 delivered at outside institution and neonatal respiratory morbidity was not obtained from chart review. 1 delivery at institution missing outcome from chart.~No app: 12 delivered at outside institution and neonatal respiratory morbidity was not obtained from chart review. 2 deliveries at institution missing outcome from chart.

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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