NCT04488055

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
488

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2020

Longer than P75 for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 20, 2020

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 27, 2020

Completed
3 months until next milestone

Study Start

First participant enrolled

October 15, 2020

Completed
4.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 10, 2025

Completed
7 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 17, 2025

Completed
Last Updated

November 4, 2025

Status Verified

October 1, 2025

Enrollment Period

4.9 years

First QC Date

July 20, 2020

Last Update Submit

October 31, 2025

Conditions

Keywords

National Suicide Prevention Lifeline

Outcome Measures

Primary Outcomes (1)

  • 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 Outcomes (1)

  • Suicidal behavior

    Up to 12 months

Study Arms (2)

Crisis Line Facilitation (CLF)

EXPERIMENTAL

This single-session intervention addresses the individuals' perceived barriers and facilitators of crisis line use during periods of suicidal crisis.

Behavioral: Crisis Line Facilitation (CLF)

Enhanced Usual Care (EUC)

ACTIVE COMPARATOR

Participants randomized to the EUC condition will receive a brochure (in-person, via email, or via text message) with the NSP Lifeline and a list of outpatient mental health and substance use resources and encouraged to schedule an appointment with a clinical provider if they would like to discuss any current or past symptoms.

Behavioral: Enhanced Usual Care (EUC)

Interventions

CLF is a motivational interviewing-based intervention

Crisis Line Facilitation (CLF)

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.

Enhanced Usual Care (EUC)

Eligibility Criteria

Age21 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Detroit Rescue Mission Ministries

Detroit, Michigan, 48201, United States

Location

Meridian Health Services

Waterford, Michigan, 48327, United States

Location

MeSH Terms

Conditions

SuicideAlcoholism

Condition Hierarchy (Ancestors)

Self-Injurious BehaviorBehavioral SymptomsBehaviorAlcohol-Related DisordersSubstance-Related DisordersChemically-Induced DisordersMental Disorders

Study Officials

  • Mark Ilgen, PhD

    University of Michigan

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor, Department of Psychiatry

Study Record Dates

First Submitted

July 20, 2020

First Posted

July 27, 2020

Study Start

October 15, 2020

Primary Completion

September 10, 2025

Study Completion

September 17, 2025

Last Updated

November 4, 2025

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Locations