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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04140149
Other study ID # H2019:292
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date July 6, 2021
Est. completion date February 28, 2024

Study information

Verified date August 2023
Source University of Manitoba
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will determine whether Living with Hope, a novel, 12-week coping skills class, reduces suicidal thoughts and behaviors among individuals who have made a recent suicide attempt. It is hypothesized that participants who complete the class will show significant improvements on measures of suicidal thoughts, hopelessness, and related mental health symptoms, and these improvements will be maintained over time.


Description:

As the 9th leading cause of death worldwide, suicide is a major public health concern. One of the groups as highest risk of death are those that have previously made a suicide attempt. Effective treatment following a suicide attempt is imperative for reducing the risk of suicide, with increasing evidence showing treatments that target suicide behavior are more effective at reducing risk over treatments that target related mental health difficulties (e.g., depression). However, these treatments are resource intensive and are difficult to access in Manitoba, and many individuals who have made a suicide attempt do not receive any mental health treatment. In order to ensure timely access to treatment following a suicide attempt, we have created a non-resource intensive psychoeducational skills class grounded in evidence-based suicide-specific treatment. The primary aim of this study is to examine the safety and effectiveness of a novel, 12-week cognitive behavior therapy-based, virtual psychoeducational skills class (Living with Hope) in reducing suicidal thoughts and behaviors among adults who have made a recent suicide attempt, and determine whether changes post-treatment are maintained at over time. The secondary aim is to determine whether this intervention also results in improvements on related mental health outcomes, and whether changes on these constructs mediate improvements on suicidal thoughts and behaviors. Adults ages 18 years and older who have been referred to the Living with Hope class over the 2 year study period will be invited to participate in the proposed study (anticipated n=60). Individuals are eligible for referral if they have made a suicide attempt in the past 3 months and are either seeking mental health crisis services. Participants will complete standardized measures of primary (suicidal thoughts and behaviors) and secondary outcomes (hopelessness, depressive symptoms, emotion regulation difficulties, and quality of life) at pre-treatment, mid-way through the 12-week class, post-treatment, 1-month follow-up, and 3-months follow-up. Mixed-effects linear regression will determine whether there are significant differences on outcome measures at any of these five time-points, as well as whether secondary outcomes mediate improvements on primary outcomes. All research participation will be conducted through virtual means. The proposed study would be the first in Canada to examine the effectiveness of a low-cost, targeted psychoeducational skills class in reducing suicidal thoughts and behaviors among individuals who have made a recent suicide attempt. This will set the stage for future linkage with administrative data and randomized controlled trials aimed at determining whether the Living with Hope class results in reduced suicide attempts and deaths compared to treatment as usual. If proven safe and effective through these rigorous evaluations, the Living with Hope class could be widely disseminated in the public health system to provide care to a large number of Manitobans, with the long-term goal of increasing access to timely, targeted treatment, and in turn, reducing suicides in Manitoba.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 26
Est. completion date February 28, 2024
Est. primary completion date August 30, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Made a suicide attempt in the past 3 months 2. Sought mental health crisis services, and referred to the Living with Hope program - Exclusion Criteria: 1. Not proficient in English 2. Exhibiting active psychotic symptoms 3. Significant cognitive impairment, are 4. Currently expressing anger or disappointment about the outcome of their attempt, 5. Recent history of violence or verbal aggression towards others, or are exhibiting other signs of behavior that would pose a threat to the safety or wellbeing of class participants 6. Primary substance use disorder -

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Living with Hope
12-week, CBT-based, psychoeducational skills class

Locations

Country Name City State
Canada Crisis Response Centre Winnipeg Manitoba

Sponsors (2)

Lead Sponsor Collaborator
University of Manitoba Health Sciences Centre Foundation, Manitoba

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in scores on the Beck Scale for Suicide Ideation 21 item self-report measure of the severity of past-week suicidal ideation Change from baseline to mid-treatment (approximately 7 weeks), to post-treatment (approximately 14 weeks), to 1-month follow-up, and to 3-month follow-up
Primary Change in scores on the Columbia-Suicide Severity Rating Scale Clinician-administered interview schedule designed to measure the timing and frequency of suicidal thoughts and behaviors Change from baseline to mid-treatment (approximately 7 weeks), to post-treatment (approximately 14 weeks), to 1-month follow-up, and to 3-month follow-up
Primary Suicide attempts Presence of a suicide attempt during the study or over the follow-up period, as assessed by the Columbia-Suicide Severity Rating Scale Through the duration of treatment and over follow-up period (approximately 6 months)
Secondary Change in scores on The Beck Hopelessness Scale 20-item self-report measure of past-week hopelessness and negative beliefs about the future Change from baseline to mid-treatment (approximately 7 weeks), to post-treatment (approximately 14 weeks), to 1-month follow-up, and to 3-month follow-up
Secondary Change in scores on the Patient Health Questionnaire-9 9-item self-report measure of depressive symptom severity over the past two-weeks Change from baseline to mid-treatment (approximately 7 weeks), to post-treatment (approximately 14 weeks), to 1-month follow-up, and to 3-month follow-up
Secondary Change in scores on the Difficulties in Emotion Regulation Scale 36-item measure of current emotional dysregulation difficulties Change from baseline to mid-treatment (approximately 7 weeks), to post-treatment (approximately 14 weeks), to 1-month follow-up, and to 3-month follow-up
Secondary Change in scores on the Quality of Life Enjoyment and Satisfaction Questionnaire - Short Form 16-item self-report measure of current quality of life Change from baseline to mid-treatment (approximately 7 weeks), to post-treatment (approximately 14 weeks), to 1-month follow-up, and to 3-month follow-up
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 1 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 2 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 3 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 4 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 5 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 6 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 7 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 8 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 9 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 10 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 11 of Living with Hope class session
Secondary Safety Item One item assessing the degree that the Living with Hope class session increased a participant's suicidal feelings Week 12 of Living with Hope class session
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