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Pre-intervention vs Post-intervention: Cumulative Incidence of ART Initiation 14 Days After Clinical Eligibility in Treatment Eligible HIV-infected Patients

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

Measures 6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.3660.3550.377wilsonClinicalTrials.gov
Risk in group 20.7910.7790.802wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.425-0.441-0.408newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.4630.4470.479logClinicalTrials.gov
Odds ratio, group 1 over group 20.1530.140.166logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Pre-intervention than on Post-intervention2.352.272.45from the risk difference intervalClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Pre-intervention
This study is stepped-wedge in design, so each clinic experienced a period of time before the intervention rolled out and then a time period after the intervention rolled out. Each clinic contributes time to both conditions. Clinics in the pre-intervention condition are giving the standard of care.
2,5857,066OG000ClinicalTrials.gov
Group 2Post-intervention
This study is stepped-wedge in design, so each clinic experienced a period of time before the intervention rolled out and then a time period after the intervention rolled out. Each clinic contributes time to both conditions. Clinics in the intervention (post-intervention) have experienced training, ongoing feedback and have the PIMA machine.
3,7534,747OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleCumulative Incidence of ART Initiation 14 Days After Clinical Eligibility in Treatment Eligible HIV-infected PatientsClinicalTrials.gov
DescriptionPatients may be ART eligible at the start of the study or become ART eligible for the first time in the 3 year time frame.ClinicalTrials.gov
Time frame14 daysClinicalTrials.gov
PopulationPersons who did have the opportunity for 14 days of follow up were excluded from these analyses.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleThe "START" (a Streamlined ART Initiation Strategy) StudyClinicalTrials.gov
NCT numberNCT01810289ClinicalTrials.gov
PhasesNAClinicalTrials.gov
ConditionsHIVClinicalTrials.gov
InterventionsSTARTClinicalTrials.gov
Lead sponsorUniversity of California, San FranciscoClinicalTrials.gov
Results first posted2017-02-27ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT01810289?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.