Community pharmacist intervention in depressed primary care patients (PRODEFAR study): randomized controlled trial protocol.

dc.contributor.authorRubio Valera, Maria
dc.contributor.authorSerrano Blanco, Antoni
dc.contributor.authorTravé i Mercadé, Pere
dc.contributor.authorPeñarrubia María, María Teresa
dc.contributor.authorRuiz, Mar
dc.contributor.authorMarch Pujol, Marian
dc.date.accessioned2013-06-04T18:11:46Z
dc.date.available2013-06-04T18:11:46Z
dc.date.issued2009-08-05
dc.date.updated2013-06-04T18:11:46Z
dc.description.abstractBackground: Treatment of depression, the most prevalent and costly mental disorder, needs to be improved. Non-concordance with clinical guidelines and non-adherence can limit the efficacy of pharmacological treatment of depression. Through pharmaceutical care, pharmacists can improve patients' compliance and wellbeing. The aim of this study is to evaluate the effectiveness and costeffectiveness of a community pharmacist intervention developed to improve adherence and outcomes of primary care patients with depression. Methods/design: A randomized controlled trial, with 6-month follow-up, comparing patients receiving a pharmaceutical care support programme in primary care with patients receiving usual care. The total sample comprises 194 patients (aged between 18 and 75) diagnosed with depressive disorder in a primary care health centre in the province of Barcelona (Spain). Subjects will be asked for written informed consent in order to participate in the study. Diagnosis will be confirmed using the SCID-I. The intervention consists of an educational programme focused on improving knowledge about medication, making patients aware of the importance of compliance, reducing stigma, reassuring patients about side-effects and stressing the importance of carrying out general practitioners' advice. Measurements will take place at baseline, and after 3 and 6 months. Main outcome measure is compliance with antidepressants. Secondary outcomes include; clinical severity of depression (PHQ-9), anxiety (STAI-S), health-related quality of life (EuroQol-5D), satisfaction with the treatment received, side-effects, chronic physical conditions and sociodemographics. The use of healthcare and social care services will be assessed with an adapted version of the Client Service Receipt Inventory (CSRI). Discussion: This trial will provide valuable information for health professionals and policy makers on the effectiveness and cost-effectiveness of a pharmaceutical intervention programme in the context of primary care. Trial registration: NCT00794196
dc.format.extent8 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec569495
dc.identifier.issn1471-2458
dc.identifier.pmid19656386
dc.identifier.urihttps://hdl.handle.net/2445/44028
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.1186/1471-2458-9-284
dc.relation.ispartofBmc Public Health, 2009, vol. 9, num. 284
dc.relation.urihttp://dx.doi.org/10.1186/1471-2458-9-284
dc.rightscc-by (c) Rubio Valera, Maria et al., 2009
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Farmàcia, Tecnologia Farmacèutica i Fisicoquímica)
dc.subject.classificationAtenció farmacèutica
dc.subject.classificationAtenció primària
dc.subject.classificationDepressió psíquica
dc.subject.classificationAnàlisi cost-benefici
dc.subject.classificationAssaigs clínics
dc.subject.otherPharmacy practice
dc.subject.otherPrimary health care
dc.subject.otherMental depression
dc.subject.otherCost effectiveness
dc.subject.otherClinical trials
dc.titleCommunity pharmacist intervention in depressed primary care patients (PRODEFAR study): randomized controlled trial protocol.eng
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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