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Combined TMS and Brief Cognitive Behavioral Therapy to Reduce Suicide

Primary Purpose

Suicide

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Transcranial Magnetic Stimulation
Brief Cognitive Behavioral Therapy
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Suicide focused on measuring suicide prevention, Veterans

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

-Suicide attempt or suicidal ideation with intent to make a suicide attempt within 48 hours of hospitalization as indicated on the hospital chart and confirmed by administration of the C-SSRS.

Exclusion Criteria:

  • Primary psychotic disorder
  • Bipolar disorder
  • Cognitive impairment which would interfere with adequate participation in the project (MMSE < 20).
  • For safety, participants must meet established screening criteria safety during MRI, which is implemented as a conservative measure given the application of TMS in this population, since MRI involves magnetic fields at similar intensity to those emitted from the stimulation coil. These measures require a patient not having the following (unless MRI-safe):

    • Cardiac pacemaker
    • Implanted device (deep brain stimulation) or metal in the brain, cervical spinal cord, or upper thoracic spinal cord.
  • TMS-specific exclusions are:

    • pregnancy/lactation, or planning to become pregnant during the study
    • lifetime history of moderate or severe traumatic brain injury (TBI)
    • Current unstable medical conditions
    • Current (or past if appropriate) significant neurological disorder
    • Lifetime history seizure disorder
    • Primary or secondary CNS tumors
    • Stroke
    • Cerebral aneurysm.
    • Other exclusions are conditions that would like to be worsened by TMS, such as bipolar disorder
    • Place Veterans at greater risk of seizures from TMS, such as severe and uncontrolled substance use disorder
    • Inability to participate in CBT
    • Other conditions or circumstance that, in the opinion of the investigator team, has the potential to prevent study completion and/or to have a confounding effect on outcome assessments

Sites / Locations

  • Providence VA Medical Center, Providence, RIRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

TMS + Brief Cognitive Behavioral Therapy

Sham TMS + Brief cognitive behavioral therapy

Arm Description

Combined transcranial magnetic stimulation and brief cognitive behavioral therapy for suicide

Sham Transcranial magnetic stimulation and brief cognitive behavioral therapy for suicide

Outcomes

Primary Outcome Measures

Change in Columbia Suicide Severity Rating Scale (CSSRS)
Interview administered assessment of suicide ideation and behavior. The interview consists of two subscales, an ideation and behavior subscale. The severity of ideation subscale is rated on a 5-point ordinal scale: 1 = wish to be dead, 2 = nonspecific active suicidal thoughts, 3 = suicidal thoughts with methods, 4 = suicidal intent, and 5 = suicidal intent with plan. The suicidal behavior subscale is rated on a nominal scale that includes actual, aborted, and interrupted attempts; preparatory behavior; and nonsuicidal self-injurious behavior.

Secondary Outcome Measures

Change in Beck Scale for Suicide Ideation (SSI)
A 21-item interview administered measure. The first 5 items are screeners (wish to live, wish to die, and desire to attempt suicide), followed by 14 items to assess suicidal risk factors. The last 2 items capture previous suicide attempts. Each item is rated on a 3-point scale ranging from 0 to 2 according to suicidal intensity. The SSI is scored by adding up the ratings (0-2) from the first 19 items.
Change in World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0)
The WHODAS 2.0 is a 12-question, self-administered questionnaire and generic assessment instrument for health and disability that covers six domains: Cognition (items 3 and 6), Mobility (items 1 and 7), Self-care (items 8 and 9), Getting Along (items 10 and 11), Life Activities (items 2 and 12), and Participation (items 4 and 5). Items are rated from "None," "Mild," "Moderate," "Severe," to "Extreme or cannot do," indicating difficulty over the past month.
Change in Treatment History Questionnaire
Interview based assessment of treatment use including hospitalizations, outpatient treatment, medication use, and emergency services. Participants report the number and type of outpatient, inpatient, residential, and emergency/crisis treatment received since last visit.

Full Information

First Posted
May 3, 2019
Last Updated
June 28, 2023
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT03952468
Brief Title
Combined TMS and Brief Cognitive Behavioral Therapy to Reduce Suicide
Official Title
Combined Transcranial Magnetic Stimulation and Brief Cognitive Therapy to Reduce Suicide Behavior in High-Risk Veterans
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 4, 2019 (Actual)
Primary Completion Date
April 30, 2024 (Anticipated)
Study Completion Date
April 30, 2024 (Anticipated)

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
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
High rates of Veteran suicide remain a tragedy. Rates of Veteran suicide have not decreased for 10 years, despite the best efforts of the field. Those interventions that do exist have only modest effects, which are simply insufficient for the magnitude of the problem. This proposal will combine two treatments - brief cognitive behavioral therapy (BCBT) and repetitive transcranial magnetic stimulation (TMS). Both of these interventions can reduce suicide and are available at Veterans Affairs Medical Centers across the country, yet to date no one has combined these therapies. This proposal will test the effect of this combination, and, if successful, will lead to a novel yet implementable new treatment to reduce Veteran suicide.
Detailed Description
The goal of the proposed study is to test the effect of adding Transcranial Magnetic Stimulation (TMS) to Brief Cognitive Behavioral Therapy (BCBT) to reduce Veterans' rates of suicide ideation and related behaviors. Over 20 Veterans die each day of suicide and rates have not appreciably decreased in the last ten years. BCBT is a well-established and efficacious treatment that is an extension of Cognitive Behavioral Therapy, a treatment that is widely implemented across VA health care systems. However, not all patients respond to BCBT. Thus finding ways to enhance treatment efficacy for reducing suicide is critical. Transcranial Magnetic Stimulation (TMS) may be an optimal treatment to use in conjunction with psychotherapy. TMS is a noninvasive technique that uses a pulsed magnetic field to induce neuronal depolarization in a targeted brain region, typically the left dorsolateral prefrontal cortex. TMS can reduce psychiatric symptoms associated with suicide risk in Veterans, including depression and PTSD. Furthermore, TMS is not associated with the systemic and costly side effects associated with medications used for these disorders (e.g., weight gain, diabetes, sexual side effects). The primary objective of this study is to conduct a fully-powered randomized controlled trial evaluating the effect of adding a standard TMS course of treatment to BCBT to reduce suicide behaviors in a sample of Veterans hospitalized for suicide behavior. One hundred and thirty (130) Veterans admitted to the psychiatric unit for suicide ideation or attempts will be randomly assigned to either active TMS plus BCBT or to sham TMS plus BCBT. Participants will be assessed at baseline, post treatment, six, and 12 months post hospital discharge. Efficacy of the program will be determined by examining a primary suicide composite outcome and several secondary outcomes including suicide attempt, time to first attempt, number of re-hospitalizations and severity and severity of suicidal ideation. Secondary analyses will be conducted to help identify the types of patients who will receive the most benefit from the addition of TMS to BCBT Brief Cognitive Behavioral Therapy for suicide. If successful, this study would result in a combined treatment to decrease suicide ideation and related behaviors. The proposal addresses HSRD post-deployment health priority, specifically suicide prevention and is innovative in that it will be the first study to examine efficacy of combined treatment specifically for suicide prevention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suicide
Keywords
suicide prevention, Veterans

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
130 Veterans admitted to the Providence VAMC psychiatric inpatient unit due to suicide attempt or ideation with intent to make an attempt will be recruited and randomly assigned to receive: a) active TMS+BCBT or b) sham TMS+BCBT. Both interventions will begin within the week following hospital discharge, and Veterans will be followed for 12 months post-discharge.
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
Prior to each TMS session, un-blinded study staff will attach the appropriate (i.e., active or sham) coil according to the participants' randomization code (obtained from the urn randomization computer program). This will facilitate "triple blind" stimulation, where the participant, TMS provider, and outcome rater are blind to group assignation.
Allocation
Randomized
Enrollment
130 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TMS + Brief Cognitive Behavioral Therapy
Arm Type
Active Comparator
Arm Description
Combined transcranial magnetic stimulation and brief cognitive behavioral therapy for suicide
Arm Title
Sham TMS + Brief cognitive behavioral therapy
Arm Type
Sham Comparator
Arm Description
Sham Transcranial magnetic stimulation and brief cognitive behavioral therapy for suicide
Intervention Type
Device
Intervention Name(s)
Transcranial Magnetic Stimulation
Other Intervention Name(s)
TMS
Intervention Description
Administration of rapidly fluctuating magnetic field, delivered over the dorsolateral prefrontal cortex.
Intervention Type
Other
Intervention Name(s)
Brief Cognitive Behavioral Therapy
Intervention Description
BCBT is a well-established and efficacious treatment that is an extension of Cognitive Behavioral Therapy, a treatment that is widely implemented across VA health care systems.
Primary Outcome Measure Information:
Title
Change in Columbia Suicide Severity Rating Scale (CSSRS)
Description
Interview administered assessment of suicide ideation and behavior. The interview consists of two subscales, an ideation and behavior subscale. The severity of ideation subscale is rated on a 5-point ordinal scale: 1 = wish to be dead, 2 = nonspecific active suicidal thoughts, 3 = suicidal thoughts with methods, 4 = suicidal intent, and 5 = suicidal intent with plan. The suicidal behavior subscale is rated on a nominal scale that includes actual, aborted, and interrupted attempts; preparatory behavior; and nonsuicidal self-injurious behavior.
Time Frame
12 month follow up
Secondary Outcome Measure Information:
Title
Change in Beck Scale for Suicide Ideation (SSI)
Description
A 21-item interview administered measure. The first 5 items are screeners (wish to live, wish to die, and desire to attempt suicide), followed by 14 items to assess suicidal risk factors. The last 2 items capture previous suicide attempts. Each item is rated on a 3-point scale ranging from 0 to 2 according to suicidal intensity. The SSI is scored by adding up the ratings (0-2) from the first 19 items.
Time Frame
12 month follow up
Title
Change in World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0)
Description
The WHODAS 2.0 is a 12-question, self-administered questionnaire and generic assessment instrument for health and disability that covers six domains: Cognition (items 3 and 6), Mobility (items 1 and 7), Self-care (items 8 and 9), Getting Along (items 10 and 11), Life Activities (items 2 and 12), and Participation (items 4 and 5). Items are rated from "None," "Mild," "Moderate," "Severe," to "Extreme or cannot do," indicating difficulty over the past month.
Time Frame
12 month follow up
Title
Change in Treatment History Questionnaire
Description
Interview based assessment of treatment use including hospitalizations, outpatient treatment, medication use, and emergency services. Participants report the number and type of outpatient, inpatient, residential, and emergency/crisis treatment received since last visit.
Time Frame
12 month follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: -Suicide attempt or suicidal ideation with intent to make a suicide attempt within 48 hours of hospitalization as indicated on the hospital chart and confirmed by administration of the C-SSRS. Exclusion Criteria: Primary psychotic disorder Bipolar disorder Cognitive impairment which would interfere with adequate participation in the project (MMSE < 20). For safety, participants must meet established screening criteria safety during MRI, which is implemented as a conservative measure given the application of TMS in this population, since MRI involves magnetic fields at similar intensity to those emitted from the stimulation coil. These measures require a patient not having the following (unless MRI-safe): Cardiac pacemaker Implanted device (deep brain stimulation) or metal in the brain, cervical spinal cord, or upper thoracic spinal cord. TMS-specific exclusions are: pregnancy/lactation, or planning to become pregnant during the study lifetime history of moderate or severe traumatic brain injury (TBI) Current unstable medical conditions Current (or past if appropriate) significant neurological disorder Lifetime history seizure disorder Primary or secondary CNS tumors Stroke Cerebral aneurysm. Other exclusions are conditions that would like to be worsened by TMS, such as bipolar disorder Place Veterans at greater risk of seizures from TMS, such as severe and uncontrolled substance use disorder Inability to participate in CBT Other conditions or circumstance that, in the opinion of the investigator team, has the potential to prevent study completion and/or to have a confounding effect on outcome assessments
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jennifer M Primack, PhD MA
Phone
(401) 273-7100
Ext
13400
Email
Jennifer.Primack@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Noah S Philip, MD
Phone
(401) 273-7100
Ext
6200
Email
noah.philip@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer Marie Primack, PhD MA
Organizational Affiliation
Providence VA Medical Center, Providence, RI
Official's Role
Principal Investigator
Facility Information:
Facility Name
Providence VA Medical Center, Providence, RI
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02908-4734
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Candace M Shuman
Phone
(401) 273-7100
Ext
13872
Email
Candace.Shuman@va.gov
First Name & Middle Initial & Last Name & Degree
Debra D'Allesandro, BA
Phone
(401) 273-7100
Ext
6238
Email
Debra.D'Allesandro@va.gov
First Name & Middle Initial & Last Name & Degree
Jennifer Marie Primack, PhD MA

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32251917
Citation
Bozzay ML, Primack J, Barredo J, Philip NS. Transcranial magnetic stimulation to reduce suicidality - A review and naturalistic outcomes. J Psychiatr Res. 2020 Jun;125:106-112. doi: 10.1016/j.jpsychires.2020.03.016. Epub 2020 Mar 28.
Results Reference
result
PubMed Identifier
33820628
Citation
Barredo J, Bozzay ML, Primack JM, Schatten HT, Armey MF, Carpenter LL, Philip NS. Translating Interventional Neuroscience to Suicide: It's About Time. Biol Psychiatry. 2021 Jun 1;89(11):1073-1083. doi: 10.1016/j.biopsych.2021.01.013. Epub 2021 Feb 1.
Results Reference
result
PubMed Identifier
35464651
Citation
Bozzay ML, Jiang L, Zullo AR, Riester MR, Lafo JA, Kunicki ZJ, Rudolph JL, Madrigal C, Clements R, Erqou S, Wu WC, Correia S, Primack JM. Mortality in patients with heart failure and suicidal ideation discharged to skilled nursing facilities. J Geriatr Cardiol. 2022 Mar 28;19(3):198-208. doi: 10.11909/j.issn.1671-5411.2022.03.009. No abstract available.
Results Reference
result
PubMed Identifier
33183345
Citation
Bozzay ML, Primack JM, Swearingen HR, Barredo J, Philip NS. Combined transcranial magnetic stimulation and brief cognitive behavioral therapy for suicide: study protocol for a randomized controlled trial in veterans. Trials. 2020 Nov 12;21(1):924. doi: 10.1186/s13063-020-04870-6.
Results Reference
derived

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Combined TMS and Brief Cognitive Behavioral Therapy to Reduce Suicide

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