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Action research represents a minority of all health research but is increasingly recognized as an approach that adds relevance to the health research process and its outcomes. It continues to garner attention as health systems face increasing accountability by those who fund them and those they serve and as health research funders come under increasing pressure to demonstrate not only that they generate new knowledge but that this knowledge is translated into better health and more effective health systems and services.

As has been the case in many areas where new knowledge is intended to create action, research in health has suffered from a tension between the needs of evidence-based rigour and contextual sensitivity. Health practice at the clinical, community or population levels should be founded on the best available evidence for what works, but it is mired in the provisos of what works for whom, when, where and in what circumstances. The creation of evidence-based knowledge has historically privileged various internal validities over external ones. Calls have therefore been made to increase the contextual relevance, and thus applicability, of research results by creating evidence-based practices (procedures, interventions, programmes, policies) from practice-based evidence. This includes evidence derived from real practice settings, such as clinics, hospitals, community health centres, communities and populations. It further implies that stakeholders within those settings should be equitably engaged in creating this evidence, from identifying the gaps or needs through undertaking research and interpreting research results, to implementing, evaluating and disseminating the findings. At all levels, from the clinic to the whole population, those who must act on the results of research, be they clinicians, service managers, patients, health organizations, communities or policymakers, are much more likely to do so if they have been involved in the research process and the results meet their personal or practice needs and goals. Therefore, the various levels of health research have increasingly adopted a participatory, action-oriented approach.

Action Research in Health

Health research has employed different action research traditions at its various levels. At the clinical level, Participatory Action Research, as an end-user-engaged form of implementation research, has attempted to bring together health-care providers, managers, institutional decision-makers and often patients in the creation and application of new practices and procedures to create better and more efficient health outcomes. At the community level, Community-Based Participatory Research (CBPR) has been the dominant form of action research. CBPR has been used to address immediate health issues and to redress historical mistreatment or underservice, to promote individual and community empowerment and to build community capacity to address future health issues. CBPR has thus created and translated knowledge for better health and promoted social and environmental justice. At the community level, participatory partnerships have traditionally included university-based academics working with community members, leaders, health-care providers and service organizations. At the population level, action research has historically adopted a modified form of CBPR that has attempted to include all the relevant community voices as well as those of policymakers from public health and other fields mandated to create public policy and programming geared to increase the overall health and well-being of a population. The CBPR approach accomplishes the goals of combining community relevance with scientific rigour, resulting in policies, programmes and interventions that meet the actual needs of a given population and take a form that makes it likely that people will actually benefit. In addition, it promotes policies and programmes that address the social determinants of health that constrain individuals' health behaviour choices.

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