The International Collaboration for Participatory Health Research: legitimating the science and ensuring quality

Author(s):  
Michael T. Wright

ZusammenfassungPartizipative Gesundheitsforschung (PGF) wird international – und seit einigen Jahren auch in Deutschland – zunehmend als Möglichkeit wahrgenommen, wissenschaftliche Erkenntnisse zu erzeugen, die unmittelbar zur Verbesserung von Gesundheitschancen für sozial benachteiligte Bevölkerungsgruppen beitragen. Zentrales Merkmal der PGF ist die direkte Beteiligung der Menschen am Forschungsprozess, deren Arbeits- oder Lebensverhältnisse Gegenstand der Forschung sind. Dieser Beitrag gibt einen Überblick über Ursprünge, Grundlagen und aktuelle Entwicklungen der PGF. Wissenschaftliche Literatur aus der internationalen Diskussion um die PGF wird im Sinne eines narrativen Reviews rezipiert, der Schwerpunkt liegt auf Überblicksarbeiten und Publikationen der International Collaboration for Participatory Health Research.Das Review ergibt, dass eine wachsende Anzahl von Forschenden im Gesundheitsbereich partizipativ arbeitet. Es ist auch deutlich erkennbar, dass ein eigenständiger wissenschaftlicher Diskurs und diverse Vereinigungen partizipativ Forschender sich in vielen Ländern etabliert haben. Folgende aktuelle internationale Entwicklungen sind hervorzuheben: Konsolidierung und Vernetzung, Klärung der Frage, was Partizipation in der Forschung bedeutet, Evaluation der Auswirkungen und des Mehrwerts der PGF, Weiterentwicklung der PGF in spezifischen Anwendungsbereichen und die Klärung ethischer Fragen in der PGF.


Author(s):  
Michael T. Wright ◽  
Bob Gardner ◽  
Brenda Roche ◽  
Hella von Unger ◽  
Carly Ainlay

2020 ◽  
Vol 30 (Supplement_5) ◽  
Author(s):  
◽  

Abstract Patient information material (PIM) is omnipresent in healthcare. It is used to convey information or to familiarize potential end-users to offers of support. PIM recaps or elaborates on relevant information and offers recommendation for action. However, the quality of available PIM varies. When the formal and content-related quality of PIM is suboptimal, it not only fails to be effective but can also lead to uncertainty, misunderstandings, resistance or ignorance (e.g. of a support offer). Highly complex information requires much attention on the quality of the PIM, especially with respect to end-users (e.g. vulnerable groups). Excellent communication through the use of PIM is thus essential within complex interventions. Checklists, such as 'Discern' or 'PEMAT', as well as criteria catalogues or evidence-based patient information standards, may assist in the development, quality assessment and optimization of PIM. The inclusion of the end-users is recommended but for various reasons does not often take place. The innovative “integrated, cross-sectional Psycho-Oncology” (isPO) programme, offers needs-driven, professional support to all adult, newly diagnosed cancer patients early in their sickness trajectory. IsPO was developed in 2018. It was implemented and a formative evaluated in 2019. When developing this programme, different PIM were created top-down by the programme designers. During implementation, it became evident that these PIM materials required further improvement. A testing and optimization process started using the participatory health research (PHR) approach and was completed in a five-month period. A PIM-optimisation team was founded, which included the project partners involved in the network support, self-help organisations and the external evaluation institute. A practical instrument (PIM-checklist) for optimising the isPO-PIM was designed, piloted and used for testing by end-users, isPO service providers, and experts. Based on the recommendations in the checklist, the material was revised accordingly. Additionally, the PIM was completed with the design of two new components. Four optimisation rounds were conducted. The optimized PIM was tested on its comprehensibility (for end-users) and its usability (for service providers). During the presentations, the audience is invited to comment on critical questions that may appear during optimization (e.g. timing). Afterwards, there will be a skill building part with a focus on collaborative learning (45 minutes). First, we will focus on the requirements for a practical instrument that is handy for end-users, service providers and experts (mind mapping exercise). Finally, participants will be able to explore the following topics “World Café” discussion: (1) how to plan, conduct and communicate the development of optimization of PIM in a CI program, (2) what needs to be considered for the optimization (e.g. team composition, resources), and (3) how to continuously achieve end-userś participation. Key messages Excellent PIM are essential for a complex interventiońs success in practice and must include information and foster actionability. the iterative PIM design processes benefits from high user participation.


BMJ Open ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. e031187 ◽  
Author(s):  
Maria-Jose Santana ◽  
Sandra Zelinsky ◽  
Sadia Ahmed ◽  
Chelsea Doktorchik ◽  
Matthew James ◽  
...  

ObjectivesThe overall goal of this study is to identify priorities for cardiovascular (CV) health research that are important to patients and clinician-researchers. We brought together a group of CV patients and clinician-researchers new to patient-oriented research (POR), to build a multidisciplinary POR team and form an advisory committee for the Libin Cardiovascular Institute of Alberta.DesignThis qualitative POR used a participatory health research paradigm to work with participants in eliciting their priorities. Therefore, participants were involved in priority setting, and analysis of findings. Participants also developed a plan for continued engagement to support POR in CV health research.SettingLibin Cardiovascular Institute of Alberta, Cumming School of Medicine, University of Calgary, Canada.ParticipantsA total of 23 participants, including patients and family caregivers (n=12) and clinician-researchers (n=11).ResultsParticipants identified barriers and facilitators to POR in CV health (lack of awareness of POR and poor understanding on the role of patients) and 10 research priorities for improving CV health. The CV health research priorities include: (1) CV disease prediction and prevention, (2) access to CV care, (3) communication with providers, (4) use of eHealth technology, (5) patient experiences in healthcare, (6) patient engagement, (7) transitions and continuity of CV care, (8) integrated CV care, (9) development of structures for patient-to-patient support and (10) research on rare heart diseases.ConclusionsIn this study, research priorities were identified by patients and clinician-researchers working together to improve CV health. Future research programme and projects will be developed to address these priorities. A key output of this study is the creation of the patient advisory council that will provide support and will work with clinician-researchers to improve CV health.


2013 ◽  
Vol 214 ◽  
pp. 255-282 ◽  
Author(s):  
Jennifer Holdaway

AbstractIn the context of this symposium, this article reviews social science research in the emerging field of environment and health in China, with a particular focus on the impacts of pollution. It begins with a discussion of the particular nature of China's environment-related health problems, distinguishing the different challenges presented by diseases of poverty, affluence and transition. It then reviews recent developments in policy and civil society with regard to environment and health, and the extent to which work in the social sciences has advanced our knowledge of these and of state–society interactions. The article concludes with some reflections on the need for and challenges of interdisciplinary and international collaboration in this area.


2015 ◽  
Vol 25 (suppl_3) ◽  
Author(s):  
S Hartung ◽  
MT Wright ◽  
T Altgeld ◽  
G Bär ◽  
T Borde ◽  
...  

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