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Comparison · NCT04856163-8cfef163

Telelactation Support vs Ebook: Breastfeeding Exclusivity

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. Telelactation Support vs Ebook: Breastfeeding Exclusivity. Trial comparisons, record NCT04856163-8cfef163. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04856163-8cfef163

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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 10.4690.4380.501wilson
Risk in group 20.4410.410.473wilson
Risk difference, group 1 minus group 20.0277-0.01690.0722newcombe hybrid score
Risk ratio, group 1 over group 21.060.9631.17log
Odds ratio, group 1 over group 21.120.9341.34log
Number needed to treat, for one more participant with the outcome on Telelactation Support than on Ebook36.1from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Telelactation Support
Participants in the experimental group received unlimited, free telelactation visits with lactation consultants (IBCLCs) as demanded up to 24 weeks post-partum. Services were available through mobile phone app.
448955OG000
Group 2EbookParticipants in the control arm received care as usual. They also received a ebook with content on infant care.422956OG001

Outcome

Type
PRIMARY
Title
Breastfeeding Exclusivity
Description
Number of participants who report no formula use at 6 months
Time frame
6 months postpartum
Population

Source ClinicalTrials.gov

Trial

Title
The Impact of Telelactation Services on Breastfeeding Outcomes
NCT number
NCT04856163
Phases
NA
Conditions
Breastfeeding
Interventions
Telelactation support
Lead sponsor
RAND
Results first posted
2025-01-03

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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