| Literature DB >> 31514719 |
Clare I R Chandler1, Helen Burchett1, Louise Boyle1, Olivia Achonduh2, Anthony Mbonye3, Deborah DiLiberto4, Hugh Reyburn5, Obinna Onwujekwe6, Ane Haaland7, Arantxa Roca-Feltrer8, Frank Baiden9, Wilfred F Mbacham2, Richard Ndyomugyenyi10, Florence Nankya11, Lindsay Mangham-Jefferies1, Sian Clarke5, Hilda Mbakilwa12, Joanna Reynolds1, Sham Lal5, Toby Leslie5, Catherine Maiteki-Sebuguzi11, Jayne Webster5, Pascal Magnussen13, Evelyn Ansah14, Kristian S Hansen1, Eleanor Hutchinson1, Bonnie Cundill5, Shunmay Yeung1, David Schellenberg5, Sarah G Staedke5, Virginia Wiseman1,15, David G Lalloo8, Christopher J M Whitty5.
Abstract
Abstract-Rigorous evidence of "what works" to improve health care is in demand, but methods for the development of interventions have not been scrutinized in the same ways as methods for evaluation. This article presents and examines intervention development processes of eight malaria health care interventions in East and West Africa. A case study approach was used to draw out experiences and insights from multidisciplinary teams who undertook to design and evaluate these studies. Four steps appeared necessary for intervention design: (1) definition of scope, with reference to evaluation possibilities; (2) research to inform design, including evidence and theory reviews and empirical formative research; (3) intervention design, including consideration and selection of approaches and development of activities and materials; and (4) refining and finalizing the intervention, incorporating piloting and pretesting. Alongside these steps, projects produced theories, explicitly or implicitly, about (1) intended pathways of change and (2) how their intervention would be implemented.The work required to design interventions that meet and contribute to current standards of evidence should not be underestimated. Furthermore, the process should be recognized not only as technical but as the result of micro and macro social, political, and economic contexts, which should be acknowledged and documented in order to infer generalizability. Reporting of interventions should go beyond descriptions of final intervention components or techniques to encompass the development process. The role that evaluation possibilities play in intervention design should be brought to the fore in debates over health care improvement.Entities:
Keywords: Africa; Complex intervention design; Evidence based public health; Implementation science; Malaria
Year: 2016 PMID: 31514719 PMCID: PMC6176770 DOI: 10.1080/23288604.2016.1179086
Source DB: PubMed Journal: Health Syst Reform ISSN: 2328-8620
Summary of ACT Projects and Interventions Discussed in This Article
| Study Title | Study Design | Setting and Dates of Implementation | Intervention | Publications on Intervention and Trial Design, Formative Research | Publications of Intervention Effect (Including Forthcoming) |
|---|---|---|---|---|---|
| The PRIME study | Two-arm cluster-randomized trial | Uganda Public health facilities 2011–2013 | Enhanced health facility–based care for malaria and febrile illnesses in children | ||
| The REACT project, Cameroon (Research on the Economics of ACTs) | Three-arm cluster-randomized trial | Cameroon Public and mission health facilities 2010–2011 | Basic and enhanced provider interventions to improve malaria diagnosis and appropriate use of ACTs in public and mission health facilities | ||
| The REACT project, Nigeria (Research on the Economics of ACTs) | Three-arm cluster-randomized trial | Nigeria Public primary health facilities and private medicine retailers 2010–2011 | Provider and community interventions to improve malaria diagnosis using RDTs and appropriate use of ACTs in public health facilities and private-sector medicine retailers | ||
| The TACT trial (Targeting ACTs) | Three-arm cluster-randomized trial | Tanzania Public health facilities 2011–2012 | Health worker and patient-oriented interventions to improve uptake of malaria RDTs and adherence to results in primary health facilities | ||
| ACT Pharmacovigilance project | Participatory research design | Uganda Health facilities and community drug distributors 2010–2012 | Development of adverse event reporting forms for use by nonclinical workers to collect data on the effects of ACTs | ||
| RDTs for home management of malaria | Two-arm cluster-randomized trial | Uganda Community drug distributors 2010–2012 | Introduction of RDTs for the home management of malaria at the community level | ||
| RDTs for drug shop management of malaria | Two-arm cluster-randomized trial | Uganda Drug shop vendors 2010–2012 | Introduction of RDTs to drug shops to encourage the rational drug use for case management of malaria | ||
| Effect of test-based versus presumptive diagnosis in the management of fever in under-five children | Two-arm cluster-randomized trial | Ghana Public primary health facilities 2011–2012 | Test-based diagnosis of malaria with RDT with restricting ACT to children who test positive |
See the ACT Consortium website (www.actconsortium.org) for more information on each of these studies.
FIGURE 1.Phases in the Development of Complex Interventions
Examples from Case Studies of Lessons Learned for Intervention Design. Note. CMD = community medicine distributor, RDT = rapid diagnostic test.
| Defining scope: consideration of intended audience for results | In the Cameroon REACT project, the initial focus of the intervention, defined in 2008, reflected concerns about appropriate use of first-line antimalarial drugs after recent policy changes to ACTs. In 2010, the project's focus was changed to appropriate diagnosis and treatment of malaria, incorporating the use of malaria RDTs. This responded to the upcoming roll-out of RDTs by the government and questions raised by them as stakeholders and the malaria community more broadly around how this could best be supported, given findings elsewhere that basic training was insufficient to support uptake of RDT results and adherence to test results. The trial therefore set out to answer specific concerns of Cameroonian policy makers by providing information about the cost-effectiveness of introducing RDTs alongside either basic training or an enhanced training intervention, compared with existing practice without RDTs. Furthermore, the initial inclusion of private sector providers was removed after feedback from the Ministry of Health that they preferred the tests first to be introduced at public and mission facilities. |
| Defining scope: consideration of level of control | For example, in the two Ugandan trials that introduced RDTs among community medicine distributors and drug shops, the objective was to learn the effect of the intervention if all providers allocated to the intervention received the full intervention. Training and follow-up supervision were delivered by members of the research team. The intention was not to produce an off-the-shelf intervention directly applicable for scale-up. By contrast, in the Nigerian trial, which introduced RDTs at public health facilities and private pharmacies and patent medicine dealers, the objective was to learn the effect of an intervention under routine conditions. Providers were invited to training sessions but were not followed up if they did not attend, and for a school-based intervention, school teachers and students were provided with intervention ideas and materials but were encouraged to undertake whatever activities they considered feasible. The intention was to produce interventions and results that would be directly applicable in practice. The latter study was closer to an effectiveness design than the former two. |
| Evidence review: scoping to identify potential intervention components in Uganda | The Ugandan PRIME project aimed to improve the quality of health care at health facilities in order to improve health outcomes and uptake of services. The target problem was identified as multifaceted, with several components of quality of care identified as targets for improvement in the project's formative research with health workers and community members. The targets were used as a focus for reviewing evidence of previous interventions:
Interventions to improve communication of health workers with patients Interventions to improve working relationships among health workers Interventions to improve facility-based supervision or coaching of health workers Interventions to improve the way patients are received and offered services equitably Interventions to improve the management of primary health facilities |
| Formative research: utility | Formative research prior to the Ugandan trial with CMDs involved 29 in-depth interviews with CMDs, health workers, and district health officials and 13 focus group discussions with mothers, fathers, and community leaders. The research aimed to understand existing CMDs' motivations, practices, and experiences and to explore the potential for introducing RDTs into the work and profile of these voluntary workers. The findings suggested that specific liaison personnel would be required to provide support to CMDs and that acknowledgment of their work through provision of commodities to support their roles would be required to sustain motivation. |
| Formative research: challenges with “barriers” approach | First, many of the barriers identified in our research were not amenable to change within the predefined scope of the intervention. For example, where wider policy dictated that certain providers were not allowed to sell or distribute certain drugs, such as antibiotics, we were unable to meet demand for training on treatment of nonmalarial febrile illnesses. Second, even when a barrier might be amenable to change, the research focus on barriers and problems provided little to inform positive action through intervention. For example, the finding in the Cameroon formative research that clinicians considered treatment with antimalarials to be a psychological treatment suggested a need for a change in expectations of consultation outcomes but did not in itself indicate what might be effective in achieving this. Third, the focus on barriers diverted attention from the motivation and agency of those enacting the problem behaviors; the practices desired by the intervention may not be in line with their priorities and motivations. For example, the Cameroonian clinicians' motivation for prescribing antimalarial drugs was to treat the whole patient, rather than the laboratory result or the malaria parasite. This represented a fundamental conflict between the focus of the malaria policy and of the study clinicians. |
| Formative research: value of appreciative enquiry | In one of our studies in Uganda, identifying the aspirations of health workers for strengthening the quality of health care they provided gave us a framework for designing the PRIME intervention, based on their desires to strengthen technical, interpersonal, and management capacities. |
Example Components of a Logic Model of an Intervention
| Inputs (resources) | Human, financial, and material resources needed for the intervention. |
| Inputs (activities of the intervention) | Specific activities in which the target audience(s) participate, such as training activities, workshops, events, and requisition of supplies. |
| Conditions | Factors among recipients and in their environment that are expected to affect the mechanism of effect of an intervention; for example, the presence of supporting resources or leaders. |
| Outputs | Measurable proximal outputs of intervention activities; for example, knowledge or motivation of a direct or indirect target audience. |
| Outcomes | Changes that occur in the target audience(s), which can be either proximal—for example, drug use behavior, patient satisfaction—or distal—for example, community health indicators. |