A Suicide Attempt Multicomponent Intervention Treatment (SAMIT Program): study protocol for a multicentric randomised controlled trial.


Journal

BMC psychiatry
ISSN: 1471-244X
Titre abrégé: BMC Psychiatry
Pays: England
ID NLM: 100968559

Informations de publication

Date de publication:
08 Oct 2024
Historique:
received: 07 06 2024
accepted: 24 09 2024
medline: 9 10 2024
pubmed: 9 10 2024
entrez: 8 10 2024
Statut: epublish

Résumé

Suicide has become a first-order public health concern, especially following the negative impact of COVID-19 on the mental health of the general population. Few studies have analysed the effects of early psychotherapeutic interventions on subjects who have attempted suicide, and even fewer have focused on those hospitalized in non-psychiatric units after a Medically Serious Suicide Attempt (MSSA). The main aim of this study is to describe the protocol designed to evaluate the effectiveness of individual psychological treatment for patients hospitalized after an MSSA. The secondary objectives of the study are: (1) to evaluate the impact on quality of life and other psychosocial variables of patients with a recent MSSA who receive early psychological intervention; (2) to analyse the biological, psychological, and clinical impact of early psychotherapeutic treatment on subjects hospitalized after an MSSA. A longitudinal randomised controlled trial will be conducted with patients over 16 years of age admitted to two general hospitals. The case intervention group will enrol for 8-sessions of individual psychotherapy, Suicide Attempts Multi-component Intervention Treatment (SAMIT), combining Dialectical Behaviour Therapy (DBT), Mentalization-Based Therapy (MBT), and Narrative approaches, while the control group will receive a treatment-as-usual intervention (TAU). Longitudinal assessment will be conducted at baseline (before treatment), post-treatment, and 3, 6, and 12 months after. The main outcome variable will be re-attempting suicide during follow-up. Some psychotherapeutic interventions, usually implemented in outpatient, have proven to be effective in preventing suicidal behaviours. The combination of some of these may be a powerful treatment for preventing future SA in patients hospitalised after an MSSA, which is the most severely suicidal subgroup. Moreover, assessment of the biological, clinical and psychometric impact of this new intervention on patients during the first year after the attempt may help understand some of the multi-level factors associated with the effectiveness of psychotherapeutic interventions in MSSAs. The prevalence of high suicide rates requires the design of effective psychological interventions for their prevention, and also in order to design new pharmacological and psychological treatments. ClinicalTrials.gov ID: NCT06238414. Date of registration: 1st February 2024, final update is protocol version 3.0, 19th March 2024.

Sections du résumé

BACKGROUND BACKGROUND
Suicide has become a first-order public health concern, especially following the negative impact of COVID-19 on the mental health of the general population. Few studies have analysed the effects of early psychotherapeutic interventions on subjects who have attempted suicide, and even fewer have focused on those hospitalized in non-psychiatric units after a Medically Serious Suicide Attempt (MSSA). The main aim of this study is to describe the protocol designed to evaluate the effectiveness of individual psychological treatment for patients hospitalized after an MSSA. The secondary objectives of the study are: (1) to evaluate the impact on quality of life and other psychosocial variables of patients with a recent MSSA who receive early psychological intervention; (2) to analyse the biological, psychological, and clinical impact of early psychotherapeutic treatment on subjects hospitalized after an MSSA.
METHODS METHODS
A longitudinal randomised controlled trial will be conducted with patients over 16 years of age admitted to two general hospitals. The case intervention group will enrol for 8-sessions of individual psychotherapy, Suicide Attempts Multi-component Intervention Treatment (SAMIT), combining Dialectical Behaviour Therapy (DBT), Mentalization-Based Therapy (MBT), and Narrative approaches, while the control group will receive a treatment-as-usual intervention (TAU). Longitudinal assessment will be conducted at baseline (before treatment), post-treatment, and 3, 6, and 12 months after. The main outcome variable will be re-attempting suicide during follow-up.
DISCUSSION CONCLUSIONS
Some psychotherapeutic interventions, usually implemented in outpatient, have proven to be effective in preventing suicidal behaviours. The combination of some of these may be a powerful treatment for preventing future SA in patients hospitalised after an MSSA, which is the most severely suicidal subgroup. Moreover, assessment of the biological, clinical and psychometric impact of this new intervention on patients during the first year after the attempt may help understand some of the multi-level factors associated with the effectiveness of psychotherapeutic interventions in MSSAs. The prevalence of high suicide rates requires the design of effective psychological interventions for their prevention, and also in order to design new pharmacological and psychological treatments.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov ID: NCT06238414. Date of registration: 1st February 2024, final update is protocol version 3.0, 19th March 2024.

Identifiants

pubmed: 39379877
doi: 10.1186/s12888-024-06113-3
pii: 10.1186/s12888-024-06113-3
doi:

Banques de données

ClinicalTrials.gov
['NCT06238414']

Types de publication

Journal Article Clinical Trial Protocol Randomized Controlled Trial Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

666

Informations de copyright

© 2024. The Author(s).

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Auteurs

Anna Beneria (A)

Department of Mental Health, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Catalonia, Spain. anna.beneria@vallhebron.cat.
Mental Health and Addictions Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Catalonia, Spain. anna.beneria@vallhebron.cat.
Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona, Catalonia, Spain. anna.beneria@vallhebron.cat.
Department of Psychiatry and Forensic Medicine, Universitat Autònoma de Barcelona, Barcelona, Catalonia, Spain. anna.beneria@vallhebron.cat.

Anna Motger-Albertí (A)

Mental Health and Addictions Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Catalonia, Spain. anna.motger.ext@vhir.org.
Addictive Behaviors Unit, Psychiatry Department, Institute of Neurosciences, IDIBAPS. RIAPAD (Red de investigación de atención primaria en adicciones), Hospital Clínic, Health and Addictions Research Group, Barcelona, Spain. anna.motger.ext@vhir.org.

Marta Quesada-Franco (M)

Department of Mental Health, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Catalonia, Spain.
Mental Health and Addictions Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Catalonia, Spain.
Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona, Catalonia, Spain.
Department of Psychiatry and Forensic Medicine, Universitat Autònoma de Barcelona, Barcelona, Catalonia, Spain.

Gara Arteaga-Henríquez (G)

Department of Mental Health, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Catalonia, Spain.
Mental Health and Addictions Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Catalonia, Spain.
Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona, Catalonia, Spain.

Olga Santesteban-Echarri (O)

Mood Disorders Program, Foothills Medical Center, Calgary, AB, Canada.

Pol Ibáñez (P)

Mental Health and Addictions Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Catalonia, Spain.

Gemma Parramon-Puig (G)

Department of Mental Health, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Catalonia, Spain.
Mental Health and Addictions Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Catalonia, Spain.
Department of Psychiatry and Forensic Medicine, Universitat Autònoma de Barcelona, Barcelona, Catalonia, Spain.

Pedro Sanz-Correcher (P)

Psychiatry and Mental Health Department, October 12th University Hospital, Madrid, Spain.
Spanish Society of Therapy Based on Mentalization, Barcelona, Spain.

Igor Galynker (I)

Department of Psychiatry, Carl Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Josep Antoni Ramos-Quiroga (JA)

Department of Mental Health, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Catalonia, Spain.
Mental Health and Addictions Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Catalonia, Spain.
Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona, Catalonia, Spain.
Department of Psychiatry and Forensic Medicine, Universitat Autònoma de Barcelona, Barcelona, Catalonia, Spain.

Luis Pintor (L)

Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona, Catalonia, Spain.
Consultation-Liaison Psychiatry Unit, Institute of Neurosciences, Hospital Clinic, University of Barcelona, IDIBAPS, Barcelona, Spain.

Pol Bruguera (P)

Addictive Behaviors Unit, Psychiatry Department, Institute of Neurosciences, IDIBAPS. RIAPAD (Red de investigación de atención primaria en adicciones), Hospital Clínic, Health and Addictions Research Group, Barcelona, Spain.

María Dolores Braquehais (MD)

Mental Health and Addictions Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Catalonia, Spain.
Department of Psychiatry and Forensic Medicine, Universitat Autònoma de Barcelona, Barcelona, Catalonia, Spain.
School of Medicine, Universitat Internacional de Catalunya, Barcelona, Catalonia, Spain.

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