Covid 19 Research using Clinical Trials (Home Page)
Report for D013405: Suicide NIH
(Synonyms: Suicide)
Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation
Correlated Drug Terms (1)
| Name (Synonyms) | Correlation | |
|---|---|---|
| drug474 | Brief Skills for Safer Living Wiki | 1.00 |
Correlated MeSH Terms (2)
| Name (Synonyms) | Correlation | |
|---|---|---|
| D059020 | Suicidal Ideation NIH | 0.71 |
| D003863 | Depression, NIH | 0.14 |
Correlated HPO Terms (0)
| Name (Synonyms) | Correlation |
|---|
There is one clinical trial.
Clinical Trials
1 Mitigating Suicide Risk During the COVID-19 Pandemic Via Telehealth Using an Intensive Single Session of "Brief Skills for Safer Living"
Mental health concerns have been on the rise since the onset of the COVID-19 pandemic. The pandemic has worsened risk factors for suicide, including job loss, anxiety, depression, and loneliness. Timely and easy access to mental health services is a dire need, and this study will test the efficacy and feasibility of a brief clinical intervention, Brief Skills for Safer Living (Brief-SfSL), at reducing suicide risk. The goal of this study is to investigate whether Brief-SfSL, delivered online, is a suitable, acceptable and effective method for reducing suicide risk and providing timely mental health services. The results from this study will provide vital insight into effective interventions for suicide risk that are accessible and can be widely distributed.
NCT04495543 Suicidal Ideation Suicide Mental Health Issue Depression Behavioral: Brief Skills for Safer Living MeSH:Depression Suicide Suicidal Ideation
Primary Outcomes
Description: Beck Scale for Suicide Ideation is a 21-item self-report scale that quantifies suicidal ideation. Items are scored 0 to 2 and yield a total score ranging from 0 to 38. Higher scores reflect greater severity of suicidal ideation.
Measure: Change in suicidal ideation using Beck Scale for Suicide Ideation Time: From baseline to 3 months; also administered at screening, 1 week and 1 monthSecondary Outcomes
Description: The QIDS-SR is a 16-item validated self-report depression scale. Total scores range from 0 (none) to 27 (very severe).
Measure: Change in depression symptoms using the Quick Inventory of Depressive Symptoms self-report scale (QIDS-SR) Time: From baseline to 3 months; also administered at 1 week and 1 monthDescription: The GAD-7 is a brief 7-item self-report scale measuring anxiety symptoms. Total scores range from 0 to 21, with higher scores reflecting more severe anxiety.
Measure: Change in anxiety symptoms using the Generalized Anxiety Disorder 7-item scale (GAD-7) Time: From baseline to 3 months; also administered at 1 week and 1 monthDescription: The ACSS is a 20-item self-report instrument to assess the construct of acquired capability. Total scores range from 0 to 80, with higher scores reflecting greater acquired capability.
Measure: Change in Acquired Capability of Suicide Scale (ACSS) Time: From baseline to 3 months; also administered at 1 week and 1 monthDescription: The Interpersonal Needs Questionnaire is a 15-item self-report scale assessing connectedness to others and burdensomeness. Items are rated 1 to 7, with total scores ranging from 15 to 105. Higher scores reflect worse outcomes.
Measure: Change in Interpersonal Needs Questionnaire score Time: From baseline to 3 months; also administered at 1 week and 1 monthDescription: The DARS is a 26-item self-report scale measuring anhedonia across four domains. Items are scored on a 5-point Likert scale with lower total scores reflecting more severe anhedonia.
Measure: Change in Dimensional Anhedonia Rating Scale (DARS) score Time: From baseline to 3 months; also administered at 1 week and 1 monthDescription: The SDS is a brief 3-item self-report scale that probes work/school, social, and family/home functioning. Each item is scored from 0 to 10. Total scores range from 0 (unimpaired) to 30 (highly impaired).
Measure: Change in Sheehan Disability Scale (SDS) score Time: From baseline to 3 months; also administered at 1 monthDescription: Use of healthcare services will be assessed through four questions enquiring about the frequency and description of health care professional visits, use of mental health services, hospital admissions, and emergency room visits in the preceding specified time frame (1-3 months).
Measure: Change in Treatment Utilization Time: From screening to 3 months; also administered at 1 monthOther Outcomes
Description: Feasibility and Acceptability survey and interview created in-house with questions designed to collect quantitative and qualitative feedback from participants with respect to the feasibility and acceptability of the Brief-SfSL intervention.
Measure: Participant feedback on their experiences with specific aspects of the Brief-SfSL intervention Time: 3 months