Crisis Line Facilitation (CLF)
Primary Purpose
Suicide, Suicide, Attempted, Hospitals, Psychiatric
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Crisis Line Facilitation (CLF)
Enhanced Usual Care (EUC)
Sponsored by
About this trial
This is an interventional treatment trial for Suicide focused on measuring Self-Injurious Behavior, suicide prevention
Eligibility Criteria
Inclusion Criteria:
Inclusion criteria for screening (Part 1).
- adults age 18 years of age or older receiving care in an inpatient psychiatric unit at either the BC VAMC or AA VAMC;
- mention of a significant suicidal crisis within the intake note;
- medically stable and able to provide informed consent; and
- Mini-Mental State Examination (MMSE) score greater than or equal to 21.
Additional inclusion criteria for the full randomized study (Part 2):
- no reported use of the Veterans Crisis Line within the past 12-months;
- report current suicidal ideation (BSS greater than or equals 5 during the week prior to hospitalization) as reported during the screening interview.
Exclusion Criteria:
Exclusion criteria for screening and full study:
- patients who do not understand English;
- prisoners;
- patients deemed unable to provide informed consent as stated above;
- patients who recently received or are scheduled to receive electroconvulsive therapy (ECT); and
- profound psychotic symptoms and/or cognitive deficits that would prevent patients from understanding the content of the intervention and/or assessments.
Sites / Locations
- VA Ann Arbor Healthcare System, Ann Arbor, MI
- Battle Creek VA Medical Center, Battle Creek, MI
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Crisis Line Facilitation (CLF)
Enhanced Usual Care (EUC)
Arm Description
Crisis Line Facilitation
Enhanced Usual Care
Outcomes
Primary Outcome Measures
Number of Veterans Crisis Line (VCL) Contact Events Per Days at Risk
The primary data source for information regarding use of the VCL was collected via researcher-administered interview questions during the TimeLine Follow Back assessment. Participants were asked to recall how many times since the last assessment in which they contacted the VCL for any reason. For contacts that occurred, participants were asked to recall the date of these contacts and the type of contact that was made (e.g. phone call, text, or chat).
Secondary Outcome Measures
Number of Suicide Behavior Events Per Days at Risk
The primary data source for suicidal behaviors was the TimeLine Follow Back, a semi-structured researcher-administered interview. Participants were asked to report actual, interrupted, and aborted attempt events that occurred since the last study assessment. Definitions for these events were derived from the Columbia Suicide Severity Rating Scale (C-SSRS) Suicidal Behaviors subsection [also administered during the assessment], and dates for these events were entered into the TimeLine Follow Back.
Outpatient General Mental Health Clinic Visit
The primary data source for general mental health treatment service utilization was a modified version of the Treatment Services Review, an researcher-administered structured interview. Participants were asked to report whether or not they had been to a mental health clinic for therapy or medications since the last study assessment.
Full Information
NCT ID
NCT02459587
First Posted
May 29, 2015
Last Updated
July 19, 2023
Sponsor
VA Office of Research and Development
1. Study Identification
Unique Protocol Identification Number
NCT02459587
Brief Title
Crisis Line Facilitation
Acronym
CLF
Official Title
Facilitating Use of the Veterans Crisis Line in High-Risk Patients
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
March 24, 2016 (Actual)
Primary Completion Date
October 7, 2019 (Actual)
Study Completion Date
December 11, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is a randomized controlled trial (n = 301) of a new single-session intervention, called Crisis Line Facilitation (CLF), compared to an enhanced usual care condition on utilization of the Veterans Crisis Line and other mental health services as well as suicide attempt(s). All participants were recruited during an inpatient psychiatric stay for the treatment of a recent suicidal crisis and will be re-assessed at 3-, 6- and 12-months post baseline. If successful, the proposed study will provide key data on the potential efficacy of a brief tool to improve the utilization of an existing resource, the Veterans Crisis Line, to reduce suicidal behaviors in VHA patients.
Detailed Description
Veterans Health Administration (VHA) patients are at a significantly elevated risk for fatal and non-fatal suicide attempts and identifying strategies to reduce the risk of suicidal behavior among members of the military and Veterans is a high national priority. The VHA has invested extensively in suicide prevention and, as part of these efforts; the Veterans Crisis Line was developed as an important resource for Veterans and their families. Utilization of the Veterans Crisis Line has expanded steadily since it first opened and, currently, it receives over 20,000 calls per month. Despite high utilization of the Crisis Line, no data are currently available on whether use of the Veterans Crisis Line reduces an individual's likelihood of a suicide attempt or death and it is not feasible to test the efficacy of the Crisis Line in a randomized controlled trial because it is nationally available to all Veterans and their families. More importantly, the Veterans Crisis Line may not reach those individuals at most acute risk for suicide. The investigators' study team conducted a small survey of Veterans treated for recent suicidal crisis in a VHA inpatient psychiatric unit and found that less than half had ever utilized the Veterans Crisis Line and less than a third had used it within the past year. Consequently, the investigators have developed and gathered pilot data on a brief intervention designed to increase utilization of the Veterans Crisis Line among high risk patients, called Crisis Line Facilitation (CLF). This single-session intervention involves a discussion of the patient's perceived barriers of crisis line use during periods of suicidal crisis. The CLF session ends with the patient calling the Crisis Line with the therapist in the room as a way for Veterans to practice the logistics of making the call and to have direct experiences that may counter any negative beliefs about Veterans Crisis Line use. This study recruited 301 participants who were treated for a suicidal crisis in VHA inpatient psychiatric but had not recently used the Veterans Crisis Line. This study is a randomized controlled trial of the impact of CLF compared to enhanced usual care (EUC) on utilization of the Veterans Crisis Line and other mental health services as well as suicide attempt(s). All participants will be re-assessed at 3-, 6- and 12-months post baseline. Analyses will also examine the extent to which post-baseline Crisis Line use mediates the effect of random assignment to CLF on subsequent suicidal behaviors. Qualitative interviews at the end of the study will help understand barriers and facilitators of future implementation of the CLF intervention. If successful, the proposed study will provide key data on the potential efficacy of a brief intervention to improve the utilization of an existing resource, the Veterans Crisis Line, to reduce suicidal behaviors in VHA patients. Developing a brief and effective approach to encourage use of the Crisis Line has the potential to have a significant and substantial impact on suicide rates within the VHA and could be modified and exported to other populations and settings.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suicide, Suicide, Attempted, Hospitals, Psychiatric
Keywords
Self-Injurious Behavior, suicide prevention
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
307 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Crisis Line Facilitation (CLF)
Arm Type
Experimental
Arm Description
Crisis Line Facilitation
Arm Title
Enhanced Usual Care (EUC)
Arm Type
Placebo Comparator
Arm Description
Enhanced Usual Care
Intervention Type
Behavioral
Intervention Name(s)
Crisis Line Facilitation (CLF)
Intervention Description
This single session therapist-delivered intervention addresses Veterans' perceived barriers and facilitators of crisis line use during periods of suicidal crisis. The CLF session culminates with the Veteran calling the Crisis Line with the therapist in the room as a way for the Veteran to practice the logistics of making the call and to have direct experiences that may counter any negative beliefs about Crisis Line use.
Intervention Type
Behavioral
Intervention Name(s)
Enhanced Usual Care (EUC)
Intervention Description
Those in the EUC condition received the same promotional items and information about the Veterans Crisis Line (VCL) as the CLF condition. Participants were encouraged to seek help via a provider or the VCL if they felt suicidal in the future. Research staff briefly explained key information about the VCL to those in the EUC condition (e.g., the links between the VCL and the VA, the 24/7/365 availability, etc.).
Primary Outcome Measure Information:
Title
Number of Veterans Crisis Line (VCL) Contact Events Per Days at Risk
Description
The primary data source for information regarding use of the VCL was collected via researcher-administered interview questions during the TimeLine Follow Back assessment. Participants were asked to recall how many times since the last assessment in which they contacted the VCL for any reason. For contacts that occurred, participants were asked to recall the date of these contacts and the type of contact that was made (e.g. phone call, text, or chat).
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Number of Suicide Behavior Events Per Days at Risk
Description
The primary data source for suicidal behaviors was the TimeLine Follow Back, a semi-structured researcher-administered interview. Participants were asked to report actual, interrupted, and aborted attempt events that occurred since the last study assessment. Definitions for these events were derived from the Columbia Suicide Severity Rating Scale (C-SSRS) Suicidal Behaviors subsection [also administered during the assessment], and dates for these events were entered into the TimeLine Follow Back.
Time Frame
1 year
Title
Outpatient General Mental Health Clinic Visit
Description
The primary data source for general mental health treatment service utilization was a modified version of the Treatment Services Review, an researcher-administered structured interview. Participants were asked to report whether or not they had been to a mental health clinic for therapy or medications since the last study assessment.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Inclusion criteria for screening (Part 1).
adults age 18 years of age or older receiving care in an inpatient psychiatric unit at either the BC VAMC or AA VAMC;
mention of a significant suicidal crisis within the intake note;
medically stable and able to provide informed consent; and
Mini-Mental State Examination (MMSE) score greater than or equal to 21.
Additional inclusion criteria for the full randomized study (Part 2):
no reported use of the Veterans Crisis Line within the past 12-months;
report current suicidal ideation (BSS greater than or equals 5 during the week prior to hospitalization) as reported during the screening interview.
Exclusion Criteria:
Exclusion criteria for screening and full study:
patients who do not understand English;
prisoners;
patients deemed unable to provide informed consent as stated above;
patients who recently received or are scheduled to receive electroconvulsive therapy (ECT); and
profound psychotic symptoms and/or cognitive deficits that would prevent patients from understanding the content of the intervention and/or assessments.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark A. Ilgen, PhD
Organizational Affiliation
VA Ann Arbor Healthcare System, Ann Arbor, MI
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Ann Arbor Healthcare System, Ann Arbor, MI
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48105-2303
Country
United States
Facility Name
Battle Creek VA Medical Center, Battle Creek, MI
City
Battle Creek
State/Province
Michigan
ZIP/Postal Code
49037
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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