Assessing the benefits on quality of life of a multicomponent intervention for fibromyalgia syndrome in primary care : patients' and health professionals' appraisals: a qualitative study protocol
Arfuch, Victoria Mailen (Universitat Autònoma de Barcelona. Departament de Pediatria, Obstetrícia i Ginecologia i de Medicina Preventiva i Salut Pública)
Caballol Angelats, Rosa (Institut Català de la Salut)
Aguilar Martín, Carina (Institut Català de la Salut)
Carrasco Querol, Noèlia (Institut Universitari d'Investigació en Atenció Primària Jordi Gol)
Sancho Sol, Maria Cinta (Institut Català de la Salut)
González Serra, Gemma (Institut Català de la Salut)
Fusté Anguera, Immaculada (Institut Català de la Salut)
Gonçalves, A. Q (Institut Català de la Salut)
Berenguera, Anna (Institut Universitari d'Investigació en Atenció Primària Jordi Gol)

Data:	2020
Resum:	Fibromyalgia syndrome (FMS) is a complex condition still scarcely understood and with ambiguity when prescribing treatment. Both patients and healthcare providers can supply valuable information for the development of new treatment strategies. The qualitative narrative analysis of participant's accounts is potentially helpful to reveal new insights about their opinions, needs, and experiences and, consequently, to model healthcare interventions accurately. International treatment guidelines suggest a promising future for multicomponent intervention (MI) approaches for FMS. This study aims to assess the benefits of a MI for patients with FMS in the context of primary care (PC) in Terres de L'Ebre, Catalonia (Spain). Furthermore, it is intended to detect the overall perception of effectiveness and to understand patients' lived experience and its impact on the quality of life. Qualitative research from a socioconstructivism paradigm perspective and a Hermeneutic Phenomenological method. For data collection, four focus group discussions (FGDs) of 8-12 people (2 FGDs of patients and 2 of professionals) and 10-12 key informant interviews with the participants in the MI group will be carried out. All the information will be recorded and verbatim transcribed to perform an interpretive thematic analysis. This study protocol has been approved by the Clinical Research Ethics Committee from the IDIAPJGol Institute, on 25 April 2018 (code P18/068), according to the Declaration of Helsinki/Tokyo. All participants will receive oral/written information about the study, and they will be required to sign an informed consent sheet. Data anonymity will be guaranteed. Dissemination will be carried out through publications in scientific journals, presentations in academic meetings, workshops and through the local and national media. ClinicalTrials. gov: ; Pre-results.
Ajuts:	Instituto de Salud Carlos III FI19/00254 Instituto de Salud Carlos III PI1800943
Drets:	Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original.
Llengua:	Anglès
Document:	Article ; recerca ; Versió publicada
Matèria:	Rheumatology ; Qualitative research ; Primary care ; Public health
Publicat a:	BMJ open, Vol. 10 (november 2020) , ISSN 2044-6055

DOI: 10.1136/bmjopen-2020-039873
PMID: 33177139

7 p, 354.5 KB

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