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dc.contributor.authorVázquez, Fernando L.
dc.contributor.authorTorres, Ángela J.
dc.contributor.authorDíaz, Olga
dc.contributor.authorPáramo, Mario
dc.contributor.authorOtero, Patricia
dc.contributor.authorBlanco Seoane, Vanessa
dc.contributor.authorLópez, Lara
dc.date.accessioned2024-02-08T18:49:07Z
dc.date.available2024-02-08T18:49:07Z
dc.date.issued2018
dc.identifier.citationVázquez, F.L., Torres, Á., Díaz, O. et al. Cognitive behavioral intervention via a smartphone app for non-professional caregivers with depressive symptoms: study protocol for a randomized controlled trial. Trials 19, 414 (2018). https://doi.org/10.1186/s13063-018-2793-2es_ES
dc.identifier.issn1745-6215
dc.identifier.urihttp://hdl.handle.net/2183/35541
dc.description.abstract[Abstract] Background: Although major depression is a frequent disorder in non-professional caregivers and there are effective psychological interventions to prevent it, caregivers have difficulty accessing them. Interventions for depression applied through an app could improve accessibility; yet, to date, adherence to such interventions has been low. The objectives of this study are to (1) evaluate the efficacy of a cognitive behavioral depression prevention intervention administered through a smartphone app with and without telephone conference calls, (2) analyze the mediators of the change in the incidence of depression and depressive symptoms, and (3) assess adherence and satisfaction with the interventions. Methods: A randomized controlled clinical trial will be conducted. Caregivers with elevated symptoms will be randomly assigned to a cognitive behavioral intervention administered by a smartphone app (CBIA) group, a CBIA plus telephone conference calls (TCCs) group (CBIA + TCC), or an attention control group. Each condition will consist of approximately 58 participants. Both interventions will be administered in five modules through a smartphone app and the CBIA + TCC group will receive additional TCCs in group format (four sessions of 30 min each). Trained blind assessors will conduct pretreatment, post-treatment and follow-up assessments at 1, 3, 6, and 12 months. Discussion: This study will provide evidence of the efficacy of a cognitive behavioral intervention to prevent depression in caregivers with elevated depressive symptoms administered through a smartphone app and the impact of feedback applied through conference calls to increase program adherence and efficacy. If the results were favorable, it would mean that we have developed a more effective, accessible, and clinically useful preventive depression intervention than the currently available ones for many present and future caregivers.es_ES
dc.description.sponsorshipThis study is funded by grant PSI2016–79041-P from the Ministry of Economy, Industry and Competitiveness of Spain. This funding source had no role in the design of this study and will not have any role during its execution, data collection, analyses, interpretation of the data, decision to submit results, or preparation of the manuscriptes_ES
dc.language.isoenges_ES
dc.publisherSpringer Naturees_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/PSI2016-79041-P/ES/UN ENSAYO CONTROLADO ALEATORIZADO SOBRE LA EFICACIA DE UNA INTERVENCION COGNITIVO-CONDUCTUAL POR APP PARA SMARTPHONES PARA CUIDADORES CON SINTOMAS DEPRESIVOSes_ES
dc.relation.urihttps://doi.org/10.1186/s13063-018-2793-2es_ES
dc.rightsAtribución 4.0 Internacional (CC BY)es_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectNon-professional caregiverses_ES
dc.subjectAppes_ES
dc.subjectSmartphonees_ES
dc.subjectDepressiones_ES
dc.subjectPreventiones_ES
dc.subjectAdherence to the interventiones_ES
dc.subjectStudy protocoles_ES
dc.titleCognitive Behavioral intervention Via a Smartphone App for Non-Professional Caregivers with Depressive Symptoms: Study Protocol for a Randomized Controlled Triales_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/openAccesses_ES
UDC.journalTitleTrialses_ES
UDC.volume19es_ES
UDC.issue414es_ES


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