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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03677882
Other study ID # VASaltLakeCity
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date December 18, 2018
Est. completion date January 31, 2023

Study information

Verified date February 2024
Source VA Salt Lake City Health Care System
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine whether a Brief Mind-Body Bridging Intervention for Suicidal Ideation (MBB-SI) will result in short or longer-term reduction of psychological factors associated with suicidal ideation (SI) and/or suicide-related behaviors (SRB's) compared to Treatment as Usual (TAU).


Recruitment information / eligibility

Status Terminated
Enrollment 13
Est. completion date January 31, 2023
Est. primary completion date January 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Subjects will be Veterans aged 18-80 admitted to Substance Abuse Residential Rehabilitation Treatment Program (SARRTP) with addictive disorders and/or co-occurring psychiatric disorder with suicide risk factors. Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Mind Body Bridging Group Session
Participants assigned to TAU + MBB will will receive treatment from the Suicide Prevention Team and the Mental Health Service, AND will be asked to participate in consisting of three to eight 60-minute sessions that will occur consecutively. Each group will be led by a trained MBB facilitator. Participants will receive a workbook at the beginning of the training that contains an explanation of all the major concepts involved in Mind Body Bridging. The workbook has homework assignments to be completed daily between group sessions.

Locations

Country Name City State
United States George E. Wahlen Department of Veterans Affairs Medical Center Salt Lake City Utah

Sponsors (2)

Lead Sponsor Collaborator
VA Salt Lake City Health Care System Mind Body Bridging Charity

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in frequency and/or intensity of suicidal ideation Determine if there is a significant difference in the frequency and/or intensity of suicidal ideation, as measured by the Beck Scale for Suicide Ideation (BSS) among the MBB-SI + TAU cohort compared to the TAU. We will use the total BSS score, ranging from 0 to 38. Increased scores reflect greater suicide risk. Weekly during the intervention, one-month post-intervention, three months post-intervention, six months post-intervention
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