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Comparison · NCT03360539-6267a9b6

Treatment - Participation in Nurse Family Partnership vs Control: Number of Participants With a Tdap Vaccination (27-36 Weeks)

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 vs Control: Number of Participants With a Tdap Vaccination (27-36 Weeks). Trial comparisons, record NCT03360539-6267a9b6. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03360539-6267a9b6

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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 10.3360.3180.354wilson
Risk in group 20.3310.3060.357wilson
Risk difference, group 1 minus group 20.00455-0.02640.035newcombe hybrid score
Risk ratio, group 1 over group 21.010.9241.11log
Odds ratio, group 1 over group 21.020.8891.17log
Number needed to treat, for one more participant with the outcome on Treatment - Participation in Nurse Family Partnership than on Control220from 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
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.
9142,723OG000
Group 2ControlControl group members have access to the standard of care and whatever other programs and services are available in the community.4461,347OG001

Outcome

Type
SECONDARY
Title
Number of Participants With a Tdap Vaccination (27-36 Weeks)
Description
Received Tdap vaccination at 27-36 weeks' gestation.~Our original prenatal screening outcome variable included the obstetric panel (D \[Rh\], RBC antibody screen, CBC, urine culture, urinalysis), STI screenings (HIV, syphilis, hepatitis B, chlamydia if \<25, gonorrhea if \<25), Group B strep screening, and glucose screening. However, since most participants had already completed their first prenatal visit prior to enrolling in the trial (when many of these tests are performed), it was not appropriate to include first-visit tests as outcomes. We therefore modified the outcome to instead use three clinically relevant measures that could occur after enrollment: glucose screening, Group B strep screening, and Tdap vaccination. These outcomes are reported as they appear in the published papers.
Time frame
At 27-36 weeks' gestation of index pregnancy; 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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