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Theta-Burst Neuromodulation for PTSD (TBS)

Primary Purpose

Chronic Post-Traumatic Stress Disorder

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Theta burst stimulation
Sham stimulation
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 Chronic Post-Traumatic Stress Disorder focused on measuring Quality of Life, Post-Traumatic Stress Disorder, Transcranial Magnetic Stimulation, Feasibility studies

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of chronic PTSD according to DSM-5 criteria
  • Veteran (male or female)
  • age between 18-70 years
  • clinically symptomatic despite ongoing stable treatment regimens for at least 6 weeks prior to study procedures
  • capable of independently reading and understanding patient information materials and providing informed consent

Exclusion Criteria:

  • Cardiac pacemaker
  • implanted device (deep brain stimulation) or metal in the brain
  • cervical spinal cord
  • or upper thoracic spinal cord
  • 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, or lifetime history of:

    • seizure disorder
    • primary or secondary CNS tumors
    • stroke
    • cerebral aneurysm
    • primary psychotic disorder
    • bipolar I disorder
    • active moderate/severe substance use disorders (within the last month, excluding nicotine/caffeine
    • active suicidal intent or plan

Sites / Locations

  • Providence VA Medical Center, Providence, RI

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Active Comparator

Arm Label

Sham Stimulation

Active Stimulation

Arm Description

A sham coil is being used to compare against active coil.

An active coil is being used to compare against sham coil.

Outcomes

Primary Outcome Measures

Number of Participants Retained, a Measure of Acceptability of TBS Procedures
Measurement of TBS acceptability, measured using participant retention rates (all-cause discontinuation)

Secondary Outcome Measures

Change in Quality of Life Due to TBS Treatment
Change in the quality of life, using the quality of life questionnaire QLESQ - Quality of Life Enjoyment and Satisfaction Questionnaire (General Quality of Life Index). A self-report scale covering multiple domains (physical health, subjective feelings, leisure time activities, social relationships, treatment satisfaction) The General Quality of Life Index took the mean of all domains. Scores range from 0-5, with higher scores indicating higher quality of life.
Change in PTSD Symptom Severity
Change in PTSD symptoms measured by the Clinician Administered PTSD Scale for DSM-5 (CAPS-5). The CAPS-5 is a structured interview to measure for PTSD symptom change and presence/absence of PTSD, items rated 0 = 'absent' to 4 = 'extreme/incapacitating,' total symptom severity score is calculated by summing severity scores for the 20 DSM-5 PTSD symptoms. Higher scores indicate more severe PTSD symptoms.
Change in Social/Occupational Functioning (QOL/SOF) Due to TBS Treatment
Change measured using the social/occupational functioning assessment scale (SOFAS). Clinician rating of social & occupational functioning. Scale of 0-100 with higher scores indicating higher functioning.

Full Information

First Posted
April 29, 2016
Last Updated
March 14, 2019
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT02769312
Brief Title
Theta-Burst Neuromodulation for PTSD
Acronym
TBS
Official Title
Pilot Testing of Theta-Burst Neuromodulation for Chronic PTSD
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
April 1, 2016 (Actual)
Primary Completion Date
December 19, 2017 (Actual)
Study Completion Date
December 19, 2017 (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
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the proposed study is to evaluate initial feasibility and efficacy of Theta Burst Transcranial Magnetic Stimulation (TBS) as an adjunct treatment for Veterans with PTSD. Primary outcomes measures include a feasibility of TBS procedures, with secondary outcome measures focusing on changes in PTSD symptom severity and quality of life and social/occupation functioning.
Detailed Description
The purpose of the proposed study is to evaluate the feasibility of theta burst transcranial magnetic stimulation (TBS) as an adjunct treatment for Veterans with PTSD. This project will result in development of methods needed to conduct an adequately powered, randomized controlled study of TBS for PTSD, which will assess the relationship between change in symptoms and quality of life. It will also lay the foundation for subsequent rehabilitation studies combining neuromodulation and psychotherapy in the longer term. TBS has several advantages compared to standard repetitive Transcranial Magnetic Stimulation (rTMS), including its ability to deliver large numbers of stimulation pulses in a shorter time period, and a stimulation pattern that may specifically affect key brain regions involved in PTSD. The significance of this research is the development of a novel, non-invasive brain stimulation approach for PTSD recovery. This project will provide the foundation for the development of methods needed to conduct an adequately powered, randomized controlled study of TBS for PTSD to ultimately develop brain stimulation techniques that can be combined with evidence-based psychotherapy, to develop a more powerful, individualized rehabilitation option for Veterans with PTSD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Post-Traumatic Stress Disorder
Keywords
Quality of Life, Post-Traumatic Stress Disorder, Transcranial Magnetic Stimulation, Feasibility studies

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sham Stimulation
Arm Type
Sham Comparator
Arm Description
A sham coil is being used to compare against active coil.
Arm Title
Active Stimulation
Arm Type
Active Comparator
Arm Description
An active coil is being used to compare against sham coil.
Intervention Type
Device
Intervention Name(s)
Theta burst stimulation
Intervention Description
Theta burst transcranial magnetic stimulation
Intervention Type
Device
Intervention Name(s)
Sham stimulation
Intervention Description
Sham Theta burst transcranial magnetic stimulation
Primary Outcome Measure Information:
Title
Number of Participants Retained, a Measure of Acceptability of TBS Procedures
Description
Measurement of TBS acceptability, measured using participant retention rates (all-cause discontinuation)
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
Change in Quality of Life Due to TBS Treatment
Description
Change in the quality of life, using the quality of life questionnaire QLESQ - Quality of Life Enjoyment and Satisfaction Questionnaire (General Quality of Life Index). A self-report scale covering multiple domains (physical health, subjective feelings, leisure time activities, social relationships, treatment satisfaction) The General Quality of Life Index took the mean of all domains. Scores range from 0-5, with higher scores indicating higher quality of life.
Time Frame
Baseline and end of double-blind period (2 weeks)
Title
Change in PTSD Symptom Severity
Description
Change in PTSD symptoms measured by the Clinician Administered PTSD Scale for DSM-5 (CAPS-5). The CAPS-5 is a structured interview to measure for PTSD symptom change and presence/absence of PTSD, items rated 0 = 'absent' to 4 = 'extreme/incapacitating,' total symptom severity score is calculated by summing severity scores for the 20 DSM-5 PTSD symptoms. Higher scores indicate more severe PTSD symptoms.
Time Frame
Baseline and end of double-blind period (2 weeks)
Title
Change in Social/Occupational Functioning (QOL/SOF) Due to TBS Treatment
Description
Change measured using the social/occupational functioning assessment scale (SOFAS). Clinician rating of social & occupational functioning. Scale of 0-100 with higher scores indicating higher functioning.
Time Frame
Baseline and end of double-blind period (2 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of chronic PTSD according to DSM-5 criteria Veteran (male or female) age between 18-70 years clinically symptomatic despite ongoing stable treatment regimens for at least 6 weeks prior to study procedures capable of independently reading and understanding patient information materials and providing informed consent Exclusion Criteria: Cardiac pacemaker implanted device (deep brain stimulation) or metal in the brain cervical spinal cord or upper thoracic spinal cord 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, or lifetime history of: seizure disorder primary or secondary CNS tumors stroke cerebral aneurysm primary psychotic disorder bipolar I disorder active moderate/severe substance use disorders (within the last month, excluding nicotine/caffeine active suicidal intent or plan
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Noah S. Philip, MD
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
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31230462
Citation
Philip NS, Barredo J, Aiken E, Larson V, Jones RN, Shea MT, Greenberg BD, van 't Wout-Frank M. Theta-Burst Transcranial Magnetic Stimulation for Posttraumatic Stress Disorder. Am J Psychiatry. 2019 Nov 1;176(11):939-948. doi: 10.1176/appi.ajp.2019.18101160. Epub 2019 Jun 24.
Results Reference
derived

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Theta-Burst Neuromodulation for PTSD

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