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Comparison · NCT04428385-1b9ddfa1

Arm 1 (Control) vs Arm 2 (Consumer-directed and Provider-directed Intervention): ACT (Artemisinin Combination Therapy) Use Among Untested Participants

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. Arm 1 (Control) vs Arm 2 (Consumer-directed and Provider-directed Intervention): ACT (Artemisinin Combination Therapy) Use Among Untested Participants. Trial comparisons, record NCT04428385-1b9ddfa1. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04428385-1b9ddfa1

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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 10.5530.5190.586wilson
Risk in group 20.6020.5680.635wilson
Risk difference, group 1 minus group 2-0.0495-0.0967-0.00207newcombe hybrid score
Risk ratio, group 1 over group 20.9180.8450.997log
Odds ratio, group 1 over group 20.8160.6720.992log
Number needed to treat, for one fewer participant with the outcome on Arm 1 (Control) than on Arm 2 (Consumer-directed and Provider-directed Intervention)20.210.3484from the risk difference interval

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Arm 1 (Control)RDTs available at study-recommended price, providers trained on mobile reporting app462836OG000
Group 2Arm 2 (Consumer-directed and Provider-directed Intervention)
providers receive a small payment for each RDT that they perform and consumers with a positive test are eligible for a subsidy on a quality-assured ACT, RDTs are available at study recommended price~Testing incentive: A small incentive will be paid to the provider each time they perform a malaria rapid diagnostic test.~Conditional artemisinin combination therapy subsidy: An additional discount on WHO-approved quality assured ACTs will be offered to individuals with a positive RDT.
498827OG001

Outcome

Type
SECONDARY
Title
ACT (Artemisinin Combination Therapy) Use Among Untested Participants
Description
Number of participants who are not tested for malaria (did not test in the shop or have documentation of a test) and purchased an ACT.
Time frame
Day of enrollment
Population
Only untested participants are included.

Source ClinicalTrials.gov

Trial

Title
Malaria Diagnostic Testing and Conditional Subsidies to Target ACTs in the Retail Sector: TESTsmART Aim 2 - Nigeria
NCT number
NCT04428385
Phases
NA
Conditions
Malaria, Febrile Illness
Interventions
Testing incentive, Conditional artemisinin combination therapy subsidy
Lead sponsor
Duke University
Results first posted
2024-05-06

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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