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Experiences of patients advising on mental health research: qualitative study in South-East European countries

BACKGROUND: Although patient and carer involvement in research is well-developed in many countries, this area has been largely overlooked in South-East European countries. AIMS: To explore experiences of patients participating in newly set up lived experience advisory panels (LEAPs) within a Europea...

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Detalles Bibliográficos
Autores principales: Repišti, Selman, Majstorović, Tihana, Ramadani, Fjolla, Zebić, Mirjana, Novotni, Ljubisha, Jovanović, Nikolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8811779/
http://dx.doi.org/10.1192/bjo.2021.1077
Descripción
Sumario:BACKGROUND: Although patient and carer involvement in research is well-developed in many countries, this area has been largely overlooked in South-East European countries. AIMS: To explore experiences of patients participating in newly set up lived experience advisory panels (LEAPs) within a European Commission funded, large-scale, multi-country mental health research project that focused on improving treatment of individuals with psychosis. METHOD: Twenty-one mental health patients were individually interviewed across five countries: Bosnia and Herzegovina, Kosovo, Montenegro, North Macedonia and Serbia. Topic guides covered the experience of participating in LEAPs and their sustainability. Data were analysed by framework analysis. RESULTS: Seven themes were identified about participating in LEAPs: predominantly positive evaluation, high levels of participant motivation, therapeutic benefits for participants, few challenges, various future perspectives, positive appraisal of the research project and mixed reflections on mental healthcare. Overall, patients’ experiences were positive and enabled them to feel empowered. Patients expressed interest in remaining involved in advisory panels. Additionally, they felt that they could potentially contribute to the work of non-government organisations. CONCLUSIONS: This study is among the few studies exploring patient participation in research projects, and the first such study conducted in South-East European countries. Patients are highly motivated for this engagement, which has the potential to empower them to take on new social roles. Significant efforts at the national level are needed in each country, to make patient involvement in research standard practice.