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

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 psychosoc...

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Autores: Roberto, Natalia, Vázquez, Mireia, Radua, Joaquim, Pariente, José Carlos, Muñoz-Moreno, Emma, Laredo, Carlos, Ruiz Veguilla, Miguel, Grande, Iria
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2023
País:España
Institución:Universidad de Sevilla (US)
Repositorio:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/173686
Acceso en línea:https://hdl.handle.net/11441/173686
https://doi.org/10.1016/j.sjpmh.2023.05.001
Access Level:acceso abierto
Palabra clave:Suicide
Protocol
Safety intervention
Psychosocial functionality
Cognition
Quality of life
Clinical status
Neuroimaging
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spelling Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocolRoberto, NataliaVázquez, MireiaRadua, JoaquimPariente, José CarlosMuñoz-Moreno, EmmaLaredo, CarlosRuiz Veguilla, MiguelGrande, IriaSuicideProtocolSafety interventionPsychosocial functionalityCognitionQuality of lifeClinical statusNeuroimagingBackground 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.Elsevier España SluPsiquiatría2023info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttps://hdl.handle.net/11441/173686https://doi.org/10.1016/j.sjpmh.2023.05.001reponame:idUS. Depósito de Investigación de la Universidad de Sevillainstname:Universidad de Sevilla (US)InglésSpanish journal of psychiatry and mental health.https://www.sciencedirect.com/science/article/pii/S2950285323000017?via%3Dihubinfo:eu-repo/semantics/openAccessoai:idus.us.es:11441/1736862026-06-17T12:51:07Z
dc.title.none.fl_str_mv Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol
title Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol
spellingShingle Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol
Roberto, Natalia
Suicide
Protocol
Safety intervention
Psychosocial functionality
Cognition
Quality of life
Clinical status
Neuroimaging
title_short Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol
title_full Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol
title_fullStr Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol
title_full_unstemmed Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol
title_sort Safety intervention for improving functioning in suicidal attempters (STRONG): A secondary prevention study. Study rationale and research protocol
dc.creator.none.fl_str_mv Roberto, Natalia
Vázquez, Mireia
Radua, Joaquim
Pariente, José Carlos
Muñoz-Moreno, Emma
Laredo, Carlos
Ruiz Veguilla, Miguel
Grande, Iria
author Roberto, Natalia
author_facet Roberto, Natalia
Vázquez, Mireia
Radua, Joaquim
Pariente, José Carlos
Muñoz-Moreno, Emma
Laredo, Carlos
Ruiz Veguilla, Miguel
Grande, Iria
author_role author
author2 Vázquez, Mireia
Radua, Joaquim
Pariente, José Carlos
Muñoz-Moreno, Emma
Laredo, Carlos
Ruiz Veguilla, Miguel
Grande, Iria
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Psiquiatría
dc.subject.none.fl_str_mv Suicide
Protocol
Safety intervention
Psychosocial functionality
Cognition
Quality of life
Clinical status
Neuroimaging
topic Suicide
Protocol
Safety intervention
Psychosocial functionality
Cognition
Quality of life
Clinical status
Neuroimaging
description 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.
publishDate 2023
dc.date.none.fl_str_mv 2023
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://hdl.handle.net/11441/173686
https://doi.org/10.1016/j.sjpmh.2023.05.001
url https://hdl.handle.net/11441/173686
https://doi.org/10.1016/j.sjpmh.2023.05.001
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Spanish journal of psychiatry and mental health.
https://www.sciencedirect.com/science/article/pii/S2950285323000017?via%3Dihub
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier España Slu
publisher.none.fl_str_mv Elsevier España Slu
dc.source.none.fl_str_mv reponame:idUS. Depósito de Investigación de la Universidad de Sevilla
instname:Universidad de Sevilla (US)
instname_str Universidad de Sevilla (US)
reponame_str idUS. Depósito de Investigación de la Universidad de Sevilla
collection idUS. Depósito de Investigación de la Universidad de Sevilla
repository.name.fl_str_mv
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