CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 2,205 enrolled
Drug / intervention
Testing incentive +1 moreother
Likely dose
Not stated in record
Key inclusion· 3
  • Fever, history of fever in last 48 hours, or suspected malaria
  • Malaria-like illness must be present at time of recruitment
  • Age older than one year
Key exclusion· 3
  • Signs of severe illness requiring immediate referral
  • Antimalarial use in the last 7 days
  • Participants <18 years without parent or legal guardian present

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04428385
NCT04428385N/ACompleted

Malaria Diagnostic Testing and Conditional Subsidies to Target ACTs in the Retail Sector: the TESTsmART Trial Aim 2

Duke University·interventional·Posted Jun 11, 2020·Updated May 6, 2024

In Brief

A clinical study evaluating Testing incentive and Conditional artemisinin combination therapy subsidy for Malaria and Febrile Illness. Completed, enrolled 2,205 participants across 1 site.

Detailed Summary

Highly subsidized first-line antimalarials (artemisinin combination therapy or ACT) are available over the counter in the private retail sector in most malaria-endemic countries. Overconsumption of ACTs purchased over the counter is rampant due to their low price, high perceived efficacy, and absence of diagnostic tools to guide drug use. The ultimate goal of the proposed work is to improve antimalarial stewardship in the retail sector, which is responsible for distributing the majority of antimalarials in sub-Saharan Africa. Through a combination of diagnosis and treatment subsidies and provider-directed incentives, this approach will align provider and customer incentives with appropriate case management and thereby improve health outcomes. The main objective of this study (Aim 2) is to test two key interventions in a random sample of private medicine retail outlets in Nigeria. This will be a cluster-randomized controlled trial where the cluster is a private retail outlet that stocks and sells WHO quality-assured ACTs. This two-arm study will test 1) a provider-directed incentive for testing and reporting in combination with a consumer-directed intervention in the form of a diagnosis-dependent ACT subsidy against 2) a comparison arm. Outlets in both arms will offer malaria diagnostic testing to customers who wish to purchase one. Information for the primary and secondary outcomes will be collected during exit interviews with eligible customers. The primary outcome will be the proportion of ACTs sold to customers with a positive diagnostic test. The main secondary outcome will be the proportion of suspected malaria cases presenting to the retail outlet that are tested. Other secondary outcomes include adherence to the RDT result amongst those tested (defined as taking a quality-assured ACT following a positive test and refraining from taking an ACT following a negative test) and appropriate case management for all suspected malaria cases (proportion tested and adhered among all suspected cases).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesNigeria

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedJun 11, 2020
Enrollment StartMar 15, 2021
Primary CompletionFeb 28, 2023
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 6.1 years ago

Interventions

Testing incentiveother

A small incentive will be paid to the provider each time they perform a malaria rapid diagnostic test.

Conditional artemisinin combination therapy subsidyother

An additional discount on WHO-approved quality assured ACTs will be offered to individuals with a positive RDT.