Evidence map›Paper›PMID 38886819›Full record

ArticleTrials2024

Financial incentives to motivate treatment for hepatitis C with direct acting antivirals among Australian adults (The Methodical evaluation and Optimisation of Targeted IncentiVes for Accessing Treatment of Early-stage hepatitis C: MOTIVATE-C): protocol for a dose-response randomised controlled study.

Parveen Fathima, Mark Jones, Reena D'Souza, James Totterdell, Nada Andric, Penelope Abbott, Richard Norman, Kirsten Howard, Wendy Cheng, Alisa Pedrana and 3 more

Abstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Parveen Fathima *Sydney School of Public Health, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia. parveen.fathima@sydney.edu.au.ORCID http://orcid.org/0000-0002-4516-4127
Mark Jones *Sydney School of Public Health, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0003-1736-1702
Reena D'SouzaWesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, WA, Australia.
James TotterdellSydney School of Public Health, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0002-9459-2566
Nada AndricSydney School of Public Health, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
Penelope AbbottDepartment of General Practice, Western Sydney University, Campbelltown, NSW, Australia.ORCID http://orcid.org/0000-0003-4865-4823
Richard NormanSchool of Population Health, Curtin University, Perth, WA, Australia.ORCID http://orcid.org/0000-0002-3112-3893
Kirsten HowardMenzies Centre for Health Policy and Economics, University of Sydney, Sydney, NSW, Australia.
Wendy ChengDepartment of Gastroenterology and Hepatology, Royal Perth Hospital, Perth, WA, Australia.
Alisa PedranaBurnet Institute, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-1998-5722
Joseph S DoyleBurnet Institute, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0001-7198-0833
Jane DaviesMenzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.
Thomas SnellingSydney School of Public Health, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0003-4670-0638

Funding

2020 Medical Research Future Fund - PPHR Initiative - Efficient use of existing medicines 2007164
6 · The paper itself

Abstract

backgroundUntreated hepatitis C virus (HCV) infection can result in cirrhosis and hepatocellular cancer. Direct-acting antiviral (DAA) therapies are highly effective and have few side effects compared to older interferon-based therapy. Despite the Australian government providing subsidised and unrestricted access to DAA therapy for chronic HCV infection, uptake has not been sufficient to meet the global target of eliminating HCV as a public health threat by 2030. This study will offer people with HCV financial incentives of varying values in order to evaluate its effect on initiation of DAA therapy in primary care.

methodsAustralian adults (18 years or older) who self-report as having current untreated HCV infection can register to participate via an automated SMS-based system. Following self-screening for eligibility, registrants are offered a financial incentive of randomised value (AUD 0 to 1000) to initiate DAA therapy. Study treatment navigators contact registrants who have consented to be contacted, to complete eligibility assessment, outline the study procedures (including the requirement for participants to consult a primary care provider), obtain consent, and finalise enrolment. Enrolled participants receive their offered incentive on provision of evidence of DAA therapy initiation within 12 weeks of registration (primary endpoint). Balanced randomisation is used across the incentive range until the first analysis, after which response-adaptive randomisation will be used to update the assignment probabilities. For the primary analysis, a Bayesian 4-parameter EMAX model will be used to estimate the dose-response curve and contrast treatment initiation at each incentive value against the control arm (AUD 0). Specified secondary statistical and economic analyses will evaluate the effect of incentives on adherence to DAA therapy, virological response, and cost-effectiveness. DISCUSSION: This project seeks to gain an understanding of the dose-response relationship between incentive value and DAA treatment initiation, while maximising the number of people treated for HCV within fixed budget and time constraints. In doing so, we hope to offer policy-relevant recommendation(s) for the use of financial incentives as a pragmatic, efficient, and cost-effective approach to achieving elimination of HCV from Australia.

trial registrationANZCTR (anzctr.org.au), Identifier ACTRN12623000024640, Registered 11 January 2023 ( https://anzctr.org.au/Trial/Registration/TrialReview.aspx?id=384923&isReview=true ).

Indexed as

Antiviral AgentsMotivationAdultAustraliaCost-Benefit AnalysisDrug CostsHepatitis C, ChronicHumansPrimary Health CareRandomized Controlled Trials as TopicTime FactorsTreatment OutcomeAntiviral AgentsAdaptive studyBayesian designDirect-acting antiviralDose–responseFinancial incentivesHepatitis CPrimary careRandomised study

Identifiers

PMID38886819
PMCPMC11181591

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.