Suicide, Attempted
Conditions
Interventions
The objective is to carry out a randomized crossover clinical trial, with a design designed to compare two groups of patients who attempted suicide and were treated at a public hospital in the city of
Sponsors
Pro Reitoria de Pesquisa - Universidade Federal de Minas Gerais
Fundação Hospitalar do Estado de Minas Gerais
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Being 18 yeas old or over; both genders; residing in the city of Belo Horizonte; have been admitted to João XXIII hospital after a suicide attempt and have a reference person who attends the first session
Exclusion criteria
Exclusion criteria: Participants cannot be considered legally incompetent; present a medical or psychiatric condition that prevents informed consent or participation in outpatient treatment, such as active psychosis or manic phase and present homicidal ideas
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in suicide attempts, measured by the question whether there were new suicide attempts after two and six months of hospital discharge | — |
Secondary
| Measure | Time frame |
|---|---|
| Reduction in suicidal ideation measured by the Brazilian Suicidal Ideation Frequency Inventory (FSII-Br), after two and six months of hospital discharge;Reduction in anxiety, depression and stress measured by the Depression, Anxiety and Stress Scale (DASS-21) after two and six months of hospital discharge;Improvement in quality of life assessed by the SF-36 Questionnaire after two and six months of hospital discharge;Improvement in reasons for living assessed by the Reasons for Living Scale ( BEMVIVER) after two and six months of hospital discharge | — |
Countries
Brazil
Contacts
Public ContactLuciana Santos
Universidade Federal de Minas Gerais
Outcome results
None listed