Ignite Creation Date:
2024-05-06 @ 1:40 PM
Last Modification Date:
2024-10-26 @ 1:18 PM
Study NCT ID:
NCT04099173
Status:
COMPLETED
Last Update Posted:
2023-05-11
First Post:
2019-07-16
Brief Title:
A Brief Mindfulness-Based Intervention for Suicidal Ideation
Sponsor:
VA Salt Lake City Health Care System
Organization:
VA Salt Lake City Health Care System
Study Overview
Official Title:
A Randomized Pilot Study of a Brief Mindfulness-Based Intervention for Suicidal Ideation
Status:
COMPLETED
Status Verified Date:
2023-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
MB-SI
Brief Summary:
The primary aim of this study is to determine whether a Brief Mindfulness-Based Intervention for Suicidal Ideation MB-SI is feasible and safe to implement The secondary aims are short and longer-term reduction in suicidal ideation SI andor suicide-related behaviors SRBs as well as improvements in mindfulness and emotional regulation measures compared to Treatment as Usual TAU
Detailed Description:
The study feasibility will be assessed through participant enrollment and retention numbers The safety be monitored by the study personnel and include reporting any adverse effects The intervention fidelity will be aided by standardizing the intervention and ensuring study personnel has the appropriate trainings Participants will completed questionnaires assessing their SI and SRB as well as mindfulness and emotional regulation measures at three time points preintervention immediately postintervention and 1-month postintervention and their results will be compared between MB-SI and TAU groups Additionally the comparisons will also be conducted for the Emergency Department ED admissions Inpatient Psychiatric Unit IPU admissions and psychiatric ED admissions
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None