Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol

Mostra el registre complet Registre parcial de l'ítem

• dc.contributor.author Roberto, Natalia
• dc.contributor.author Toll Privat, Alba
• dc.contributor.author Elices, Matilde
• dc.contributor.author Pérez Solá, Victor
• dc.contributor.author Grande, Iria
• dc.date.accessioned 2025-04-07T06:13:00Z
• dc.date.available 2025-04-07T06:13:00Z
• dc.date.issued 2023
• dc.description Data de publicació electrònica: 07-09-2023
• dc.description.abstract Background: Suicide is one of the most largely preventable causes of death worldwide. The aim of the STRONG study is to assess the effectiveness of a specific intervention (an extended Safety Planning Intervention) called iFightDepression-SURVIVE (iFD-S) in suicidal attempters by changes in psychosocial functioning. As secondary outcomes, quality of life, cognitive performance, clinical state and neuroimaging correlates will be considered. Objective: To describe the rationale and design of the STRONG study, an extension of the SURVIVE study, a national multicenter cohort about on prevention in suicidal attempters. Methods: The STRONG study is a two-year clinical trial. A total sample of 60 patients will be randomly allocated to two arms: a group will receive a iFD-S and treatment as usual (TAU) (n=30 treatment group), while another group will exclusively receive TAU (n=30 control group). There will be three study points: baseline; 3-month; and 6-month follow-up assessments, all of which will include rater-blinded evaluation of psychosocial functioning, quality of life, clinical state, cognitive performance and neuroimaging acquisition. Results: It is expected to obtain data on the efficacy of iFD-S in patients who have committed a suicide attempt. Conclusion: Results will provide insight into the effectiveness of IFD-S in suicidal attempters with respect to improvements in psychosocial functioning, quality of life, cognition, and neuroimaging correlates. Clinical trials id: NCT05655390.
• dc.description.sponsorship EV wishes to acknowledge the support from CIBER – Consorcio Centro de Investigación Biomédica en Red – (CB07/09/0004), Instituto de Salud Carlos III, the Spanish Ministry of Science and Innovation (PI18/00805, PI21/00787), Instituto de Salud Carlos III – Fondo Europeo de Desarrollo Regional (FEDER). Unión Europea. “Una manera de hacer Europa”, cofinanciado por la Unión Europea; the CERCA Program/Generalitat de Catalunya and Secretaria d’Universitats i Recerca del Departament d’Economia I Coneixement (2021 SGR 01358). Departament de Salut de la Generalitat de Catalunya, Pla Estratègic de Recerca i Innovació en Salut (PERIS) 2016-2020 (SLT006/17/00357). Thanks are also given for the support received from the European Union Horizon 2020 research and innovation program (EU.3.1.1. Understanding health, wellbeing and disease: grant no. 754907 and EU.3.1.3. Treating and managing disease: grant no. 945151). ME has a Juan de la Cierva research contract awarded by the ISCIII (FJCI-2017-31738). VP, ME, and AT want to thank unrestricted research funding from “Secretaria d’Universitats i Recerca del Departament d’Economia i Coneixement” (2017 SGR 134 to “Mental Health Research Group”), Generalitat de Catalunya (Government of Catalonia). PAS has received partial support from the Government of the Principality of Asturias PCTI-2021-2023 IDI/2021/111, the Fundación para la Investigación e Innovación Biosanitaria del Principado de Asturias (FINBA), and Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Instituto de Salud Carlos III, and Ministerio de Ciencia e Innovación. The funders had no role in the study design, decision to publish, or preparation of the manuscript.
• dc.format.mimetype application/pdf
• dc.identifier.citation Roberto N, Vazquez M, Radua J, Pariente JC, Muñoz-Moreno E, Laredo C, et al. Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol. Span J Psychiatry Ment Health. 2023 Aug 25:S2950-2853(23)00001-7. DOI: 10.1016/j.sjpmh.2023.05.001
• dc.identifier.doi http://dx.doi.org/10.1016/j.sjpmh.2023.05.001
• dc.identifier.issn 2950-2853
• dc.identifier.uri http://hdl.handle.net/10230/70094
• dc.language.iso eng
• dc.publisher Elsevier
• dc.relation.ispartof Span J Psychiatry Ment Health. 2023 Aug 25:S2950-2853(23)00001-7
• dc.relation.projectID info:eu-repo/grantAgreement/EC/H2020/754907
• dc.relation.projectID info:eu-repo/grantAgreement/EC/H2020/945151
• dc.rights © 2023 The Authors. Published by Elsevier España, S.L.U. on behalf of Sociedad Española de Psiquiatría y Salud Mental (SEPSM). This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
• dc.rights.accessRights info:eu-repo/semantics/openAccess
• dc.rights.uri http://creativecommons.org/licenses/by/4.0/
• dc.subject.keyword Clinical status
• dc.subject.keyword Cognition
• dc.subject.keyword Neuroimaging
• dc.subject.keyword Protocol
• dc.subject.keyword Psychosocial functionality
• dc.subject.keyword Quality of life
• dc.subject.keyword Safety intervention
• dc.subject.keyword Suicide
• dc.title Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol
• dc.type info:eu-repo/semantics/article
• dc.type.version info:eu-repo/semantics/publishedVersion