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Comparison · NCT03360539-06f68c9e

Treatment - Participation in Nurse Family Partnership Nurse-Family Partnership vs Control: Number of Participants With a Postpartum Visit

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. Treatment - Participation in Nurse Family Partnership Nurse-Family Partnership vs Control: Number of Participants With a Postpartum Visit. Trial comparisons, record NCT03360539-06f68c9e. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03360539-06f68c9e

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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 10.6380.6210.654wilson
Risk in group 20.6420.6190.665wilson
Risk difference, group 1 minus group 2-0.00479-0.03320.024newcombe hybrid score
Risk ratio, group 1 over group 20.9930.9491.04log
Odds ratio, group 1 over group 20.9790.8651.11log
Number needed to treat, for one fewer participant with the outcome on Treatment - Participation in Nurse Family Partnership Nurse-Family Partnership than on Control209from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Treatment - Participation in Nurse Family Partnership Nurse-Family Partnership
NFP is a prenatal and infancy home visiting program for low-income, first-time mothers and their families. Registered nurses begin visiting their clients as early in the pregnancy as possible, helping the mother-to-be make informed choices. The nurses continue visiting regularly until the child is two years old.
2,0793,261OG000
Group 2ControlControl group members have access to the standard of care and whatever other programs and services are available in the community.1,0381,616OG001

Outcome

Type
SECONDARY
Title
Number of Participants With a Postpartum Visit
Description
Number of participants with a postpartum visit in first 12 weeks after an index birth.
Time frame
Within 12 weeks after index birth; Medicaid claims
Population
Differs from randomized sample as it excludes participants with missing outcome data, an index fetal death, who withdrew, who experienced a pregnancy loss, and who could not be matched to an index pregnancy.

Source ClinicalTrials.gov

Trial

Title
Nurse-Family Partnership Impact Evaluation in South Carolina
NCT number
NCT03360539
Phases
NA
Conditions
Preterm Birth, Injuries, Maternal Behavior
Interventions
Nurse-Family Partnership
Lead sponsor
Harvard School of Public Health (HSPH)
Results first posted
2025-12-12

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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