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Suicide, Attempted clinical trials

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NCT ID: NCT01118208 Completed - Clinical trials for Medication Adherence

Blister Packaging Medication to Increase Treatment Adherence and Clinical Response

BP
Start date: September 2009
Phase: N/A
Study type: Interventional

This quantitative, interview-based study will determine if increased prescription medication adherence via blister pack administration will reduce suicide related behavior among the high risk population of patients discharged from a psychiatric inpatient unit. The aims of the project are to determine whether blister packaging medication significantly increases treatment adherence and if blister packaging significantly decreases intentional self-poisoning behavior (i.e., suicide attempts and completions). By tracking former psychiatric inpatients for 12 months post-discharge and obtaining monthly medication adherence ratings, we will determine if blister packaging (BP) medications leads to better adherence than dispensing as usual (DUA). The psychiatric patients we will be recruiting have been diagnosed with, major affective disorder, bipolar affective disorder, post-traumatic stress disorder, or schizophrenia (or any combination of these diagnoses). By tracking former psychiatric patients for 12 months post-discharge and obtaining monthly reports (self-report and medical record review) of suicide-related behaviors, we will determine if patients in the BP condition have less intentional self-poisoning behavior than those in the DAU condition.

NCT ID: NCT00763724 Completed - Depression Clinical Trials

Antidepressant Drug Exposure and Risk of Suicide Attempt Resulting in Medical Intervention in US Adults

Start date: June 2008
Phase: N/A
Study type: Observational

The primary objective of the study is to estimate the incidence of suicide attempts resulting in a medical encounter or hospitalization in seven propensity matched cohorts of subjects: patients treated with duloxetine for depression, patients treated with one of three other antidepressants or antidepressant classes (venlafaxine, SSRIs, or TCAs) for depression, patients treated with multiple antidepressants for depression (either concurrently or consecutively), depressed patients with no pharmacologic treatment, and a non-depressed general population sample.

NCT ID: NCT00736918 Completed - Suicide Attempt Clinical Trials

RCT of Post-Suicide Attempt Case Management (ACTION-J)

ACTION-J
Start date: June 2006
Phase: Phase 3
Study type: Interventional

This study will determine the effectiveness of continuous follow-up care by case manager in preventing further suicide attempts

NCT ID: NCT00735540 Completed - Clinical trials for Chronic Renal Failure

Clinical Diagnosis of Teenagers Admitted to Pediatric Departments

Start date: May 2008
Phase: N/A
Study type: Observational

This study intends to analyze the clinical characteristics of teenagers admitted to pediatric wards due to organic illness and non organic diagnosis, including patients suffering from chronic diseases and comorbidity.

NCT ID: NCT00700089 Completed - Suicide, Attempted Clinical Trials

AID-trial Assertive Intervention After Deliberate Self-harm

AID
Start date: November 2007
Phase: Phase 4
Study type: Interventional

Background Previous suicide attempts is a high-risk factor with a repetition rate between 12-30 percent. Compliance with after treatment is often poor. A systematic review by Hawton, 1999 states a lack of evidence on psychosocial interventions due to selections bias or statistical power. Objective The aim is to investigate if assertive outreach, incorporating hands-on guidance and motivational support of compliance with follow-up treatment after suicide attempts is able to reduce the frequency of non-fatal and fatal suicide acts in a one-year follow-up period. Method and Design A randomized, controlled intervention trial in a prospective design. The patients included will be randomized to either standard treatment (n = 120) or intervention treatment (N = 120), representing 6 - 8 assertive outreach contacts with a research nurse after suicide attempts or deliberate self-harm. The outreach contacts are thought of as supporting and guiding home visits towards compliance with after care or follow-up treatment Inclusion criteria Males and females, aged 12 years or older with a recent suicide attempt or act of deliberate self-harm, living independently and not diagnosed with severe mental illness (psychosis, severe dementia) Outcome The primary outcome measure is repeated fatal suicidal act (fatal or non fatal)assessed by the Danish Cause of Death Register and the rate of repeated suicide attempts/deliberate self-harm registered in the medical records by the collaborating wards and units in their routine procedure of treating people applying for help in relation to suicidal behavior.

NCT ID: NCT00664872 Completed - Suicide, Attempted Clinical Trials

Effect of Psychosocial Treatment by the Case Manager in Patients After a Suicide Attempt

Start date: August 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the case manager are effective in the treatment of suicide attempters.

NCT ID: NCT00643812 Completed - Suicide Clinical Trials

Improving Firearm Storage in Alaska Native Villages

Start date: November 2004
Phase: N/A
Study type: Interventional

Rates of suicide among young Alaska Native males are over ten-fold higher than among a similar age cohort in the rest of the United States. A high proportion of these deaths are associated with firearms. Firearms are an important part of the subsistence lifestyle of this population, however restriction of access to guns by youth may be a promising strategy to reduce the risk of suicides in this population. Previous research conducted in the first phase of this project has demonstrated that about 75% of homes in rural southwest Alaskan villages have guns, and only about 15% of these guns are locked; 6% are loaded. The aims of this specific phase of the study to execute a randomized trial of an intervention to improve firearm storage practices among residents of selected villages. Our hypothesis is that households receiving training and equipment to store firearms in gun lockers will be more likely to store their guns locked at 12 months, compared to households not receiving the intervention.

NCT ID: NCT00641498 Completed - Suicide Attempted Clinical Trials

Effectiveness of Standard Emergency Department Psychiatric Treatment Associated With Treatment Delivery by a Suicide Prevention Center

Start date: March 2007
Phase: N/A
Study type: Interventional

Very few studies have proved the effectiveness of treatment for suicide attempt patients. Our objective is to evaluate the addition of the resources of an suicide prevention centre to standard psychiatric treatment in the Emergency Department. Consecutive suicide attempt patients in 2 Emergency departments (multicenter study) were included after standard psychiatric treatment and referral. After Written informed consent, psychological assessment (depression, suicide intention) was carried out After randomisation, control patients were given an information card describing the Suicide Prevention Center (SPC); experimental patients had a first meeting with a psychologist of the SPC. To verify the hypothesis of a decrease in suicidal behaviors in the experimental group, an evaluation of these behaviors was carried out every month during a two year follow-up.

NCT ID: NCT00603421 Completed - Clinical trials for Borderline Personality Disorder

Effectiveness of a 24 Hour Phone Line on the Rate of Suicide Attempts in Borderline Patients

Start date: February 2009
Phase: N/A
Study type: Interventional

This randomized multicentric clinical trial assesses the effectiveness of 24 hour phone line on the rate of suicide attempts and self-injurious behaviors in borderline patients.

NCT ID: NCT00589641 Completed - Depression Clinical Trials

Relapse Prevention for Suicidal Dually Diagnosed Youths

CBT-RP
Start date: July 2005
Phase: Phase 1
Study type: Interventional

The purpose of this study is to develop, refine, and pilot test an augmenting cognitive behavior relapse prevention intervention (CBT-RP) for suicidal, depressed, and alcohol/substance abusing adolescents. No hypotheses are being tested, but it is expected that CBT-RP in addition to treatment as usual will result in improved outcomes relative to treatment as usual alone.