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The development of effective behaviour change interventions to support the use of malaria rapid diagnostic tests by Tanzanian clinicians
BACKGROUND: Parasitological confirmation is now recommended for all cases of suspected malaria. The roll-out of rapid diagnostic tests (RDTs) is hoped to enable this goal in low resource settings through point of care testing. However, simply making RDTs available has not led to high uptake of the t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227094/ https://www.ncbi.nlm.nih.gov/pubmed/24969367 http://dx.doi.org/10.1186/1748-5908-9-83 |
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author | Chandler, Clare IR Meta, Judith Ponzo, Célia Nasuwa, Fortunata Kessy, John Mbakilwa, Hilda Haaland, Ane Reyburn, Hugh |
author_facet | Chandler, Clare IR Meta, Judith Ponzo, Célia Nasuwa, Fortunata Kessy, John Mbakilwa, Hilda Haaland, Ane Reyburn, Hugh |
author_sort | Chandler, Clare IR |
collection | PubMed |
description | BACKGROUND: Parasitological confirmation is now recommended for all cases of suspected malaria. The roll-out of rapid diagnostic tests (RDTs) is hoped to enable this goal in low resource settings through point of care testing. However, simply making RDTs available has not led to high uptake of the tests or adherence to results by clinicians, with malaria continuing to be overdiagnosed in many settings. We undertook to design an evidence-based intervention package that would be sufficient to support the introduction of RDTs at dispensaries in Tanzania, to be evaluated through the Targeting Artemisinin Combination Therapy (TACT) cluster randomised controlled trial. METHODS: We describe five steps in our intervention design: formative research, review of existing evidence and theory, a workshop to define the intervention approach and content and results of formative research, engagement with behaviour change theory and literature, detailed design of intervention materials and piloting and pretesting of intervention materials. This involved fieldwork with a total of 19 health workers and 212 community members in northeast Tanzania. RESULTS: The formative research suggested that RDTs were a potential source of conflict in the health worker-patient interaction, but that health workers used various techniques to resolve this, including provision of antimalarial drugs for RDT-negative patients. Our reviews showed that evidence was mixed regarding the effectiveness of different methods and theories to support change in prescribing practice. Our design process is presented, drawing from this collective evidence. We describe the final TACT intervention package (including interactive small group workshops, feedback text messages, motivational text messages and patient information leaflets and posters) in terms of its programme theory and implementation theory. CONCLUSIONS: Our study suggests that evidence-based design of complex interventions is possible. The use of formative research to understand malaria overdiagnosis in context was central to the design of the intervention as well as empirical research to test materials and methods prior to implementation. The TACT interventions may be appropriate for other settings where clinicians face similar challenges with malaria diagnostics. TRIAL REGISTRATION: NCT01292707. |
format | Online Article Text |
id | pubmed-4227094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42270942014-11-12 The development of effective behaviour change interventions to support the use of malaria rapid diagnostic tests by Tanzanian clinicians Chandler, Clare IR Meta, Judith Ponzo, Célia Nasuwa, Fortunata Kessy, John Mbakilwa, Hilda Haaland, Ane Reyburn, Hugh Implement Sci Research BACKGROUND: Parasitological confirmation is now recommended for all cases of suspected malaria. The roll-out of rapid diagnostic tests (RDTs) is hoped to enable this goal in low resource settings through point of care testing. However, simply making RDTs available has not led to high uptake of the tests or adherence to results by clinicians, with malaria continuing to be overdiagnosed in many settings. We undertook to design an evidence-based intervention package that would be sufficient to support the introduction of RDTs at dispensaries in Tanzania, to be evaluated through the Targeting Artemisinin Combination Therapy (TACT) cluster randomised controlled trial. METHODS: We describe five steps in our intervention design: formative research, review of existing evidence and theory, a workshop to define the intervention approach and content and results of formative research, engagement with behaviour change theory and literature, detailed design of intervention materials and piloting and pretesting of intervention materials. This involved fieldwork with a total of 19 health workers and 212 community members in northeast Tanzania. RESULTS: The formative research suggested that RDTs were a potential source of conflict in the health worker-patient interaction, but that health workers used various techniques to resolve this, including provision of antimalarial drugs for RDT-negative patients. Our reviews showed that evidence was mixed regarding the effectiveness of different methods and theories to support change in prescribing practice. Our design process is presented, drawing from this collective evidence. We describe the final TACT intervention package (including interactive small group workshops, feedback text messages, motivational text messages and patient information leaflets and posters) in terms of its programme theory and implementation theory. CONCLUSIONS: Our study suggests that evidence-based design of complex interventions is possible. The use of formative research to understand malaria overdiagnosis in context was central to the design of the intervention as well as empirical research to test materials and methods prior to implementation. The TACT interventions may be appropriate for other settings where clinicians face similar challenges with malaria diagnostics. TRIAL REGISTRATION: NCT01292707. BioMed Central 2014-06-26 /pmc/articles/PMC4227094/ /pubmed/24969367 http://dx.doi.org/10.1186/1748-5908-9-83 Text en Copyright © 2014 Chandler et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Chandler, Clare IR Meta, Judith Ponzo, Célia Nasuwa, Fortunata Kessy, John Mbakilwa, Hilda Haaland, Ane Reyburn, Hugh The development of effective behaviour change interventions to support the use of malaria rapid diagnostic tests by Tanzanian clinicians |
title | The development of effective behaviour change interventions to support the use of malaria rapid diagnostic tests by Tanzanian clinicians |
title_full | The development of effective behaviour change interventions to support the use of malaria rapid diagnostic tests by Tanzanian clinicians |
title_fullStr | The development of effective behaviour change interventions to support the use of malaria rapid diagnostic tests by Tanzanian clinicians |
title_full_unstemmed | The development of effective behaviour change interventions to support the use of malaria rapid diagnostic tests by Tanzanian clinicians |
title_short | The development of effective behaviour change interventions to support the use of malaria rapid diagnostic tests by Tanzanian clinicians |
title_sort | development of effective behaviour change interventions to support the use of malaria rapid diagnostic tests by tanzanian clinicians |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227094/ https://www.ncbi.nlm.nih.gov/pubmed/24969367 http://dx.doi.org/10.1186/1748-5908-9-83 |
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