Martín-Iglesias, Susana http://orcid.org/0000-0001-6628-4120
Santamaría-Martín, M. Jesús
Alonso-Álvarez, Ahinoa
Rico-Blázquez, Milagros
del Cura-González, Isabel
Rodríguez-Barrientosn, Ricardo
Barberá-Martín, Aurora
Sanz-Cuesta, Teresa
Isabel Coghen-Vigueras, M.
de Antonio-Ramírez, Isabel
Durand-Rincón, Isabel
Garrido-Rodriguez, Felisa
Geijo-Rincón, María Jesús
Mielgo-Salvador, Rebeca
Morales-Montalvá, M. Soledad
Reviriego-Gutiérrez, M. Asunción
Rivero-Garrido, Carmen
Ruiz-Calabria, Micaela
Santamaría-Mechano, M. Pilar
Santiago-Fernández, Roberto
Sillero-Quintana, M. Isabel
Soto-Almendro, Beatriz
Terol-Claramonte, María
Villa-Arranz, María
Funding for this research was provided by:
ISCIII-Subdirección General de Evaluación and Fondo Europeo de Desarrollo Regional (FIS PI12/02609)
ISCIII-Subdirección General de Evaluación and Fondo Europeo de Desarrollo Regional (PI12/02020)
Article History
Received: 4 December 2017
Accepted: 1 February 2018
First Online: 26 February 2018
Ethics approval and consent to participate
: The study has been approved by the Hospital’s Clinical Research Ethics Committee (28 August 2013) and favourably evaluated by the Central Research Commission of the Primary Healthcare Management of Madrid (13 April 2012). The study will be carried out in accordance with the basic principles of the Helsinki Declaration (2013), the Good Clinical Practices (GCP) will be followed along with current Spanish legislation (Real Decreto 223/2004).Investigator commitment will be requested of all professionals that participate in the study. The investigator will duly inform the subjects that participate in the study and will request their informed consent, signed, and dated in writing. He/she will provide complete and adequate verbal and written information about the nature, purpose and possible risks and benefits of the study.Any modifications to the protocol which may impact on the conduct of the study, potential benefit of the patient or may affect patient safety, including changes of study objectives, study design, patient population, sample sizes, study procedures, or administrative aspects will require a formal amendment to the protocol. Such amendment will be agreed upon by The Unidad de Apoyo a la Investigación de la Gerencia Asistencial de Atención Primaria de la Comunidad de Madrid.
: Not applicable
: The authors declare that they have no competing interests.
: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.