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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04488055
Other study ID # HUM00164699
Secondary ID 1R01AA027513-01
Status Recruiting
Phase N/A
First received
Last updated
Start date October 15, 2020
Est. completion date June 2025

Study information

Verified date May 2024
Source University of Michigan
Contact Amanda Price, MS
Phone 734-764-3662
Email amhprice@med.umich.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research study is to learn about people who use the National Suicide Prevention (NSP) Lifeline during a suicidal crisis and those who don't. The researchers would also like to learn whether people who have experienced a suicidal crisis could benefit from participating in a therapy session about their thoughts and perceptions of the NSP Lifeline.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date June 2025
Est. primary completion date June 2025
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - Probable alcohol use disorder within the past year based on an Alcohol Use Disorders Identification Test (AUDIT) score of 16 or greater - Report of a suicide attempt within the past year OR a lifetime suicide attempt more than a year ago and current suicide ideation within the past month based on a score of 5 or greater on the Beck Scale for Suicidal Ideation (BSS) or depression in the past month as measured by the Beck Depression Inventory with a of 20 or higher. Exclusion Criteria: - Patients who do not understand English - Prisoners - Patients with profound psychotic symptoms and/or cognitive deficits that would prevent patients from understanding the content of the intervention and/or assessments.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Crisis Line Facilitation (CLF)
CLF is a motivational interviewing-based intervention
Enhanced Usual Care (EUC)
In addition to receiving the brochure, EUC condition participants will meet with a therapist (in-person or remotely) for approximately 15 minutes for a descriptive overview of the brochure.

Locations

Country Name City State
United States Detroit Rescue Mission Ministries Detroit Michigan
United States Meridian Health Services Waterford Michigan

Sponsors (2)

Lead Sponsor Collaborator
University of Michigan National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Crisis line utilization The Time Line Follow Back (TLFB) assessment will be used as the primary measure of crisis line utilization. Participants will report days of utilization. Up to 12 months
Secondary Suicidal behavior The Time Line Follow Back (TLFB) assessment will be the primary measure of suicidal behavior. Participants will report days with suicidal behavior. Up to 12 months
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