search
Back to results

The PRISM Pilot Trial for Post-Traumatic Stress Disorder

Primary Purpose

Post-Traumatic Stress Disorder (PTSD)

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
PRISM
Sponsored by
GrayMatters Health Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-Traumatic Stress Disorder (PTSD) focused on measuring PTSD

Eligibility Criteria

22 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Ages 22 to 65
  2. Any gender
  3. Diagnosis of PTSD, established according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V)
  4. 1 to 20 years since index trauma
  5. Ability to give signed, informed consent
  6. Normal or corrected-to-normal vision
  7. Normal or corrected to normal hearing
  8. Subject is able to adhere to the study schedule

Exclusion Criteria:

  1. Have completed two or more full courses of trauma-focused therapy in the past (i.e., EMDR, Prolong Exposure Therapy, etc.), eligibility will be deemed upon the clinical judgment of the investigator.
  2. Lifetime diagnosis for schizophrenia, schizoaffective disorder, schizophreniform disorder, Bipolar I disorder, or delusional disorder
  3. Any mood disorder and anxiety disorder according to DSM-5 (in addition to those described in Exclusion 2) that is the primary focus of treatment in the last 6 months prior to screening, as per the clinical judgment of the investigator
  4. Lifetime diagnosis of autism, mental retardation at the discretion of the investigator.
  5. Diagnosis of moderate or severe substance use disorder within the last 3 months of screening visit (as defined in DSM-5-substance use disorder) or at screening visit
  6. Any prescribed Benzodiazepine which cannot be ceased for the duration of the study (with a washout period of at least 2 weeks prior to the first Prism training session) or which cannot be replaced with short-acting benzodiazepines that are taken only for sleeping during the night
  7. Any psychotropic medication other than a stable dose of selective serotonin reuptake inhibitors (SSRIs) or serotonin-norepinephrine reuptake inhibitor (SNRIs)
  8. Any change in or initiation of- SSRIs or SNRIs antidepressants within the past 4 weeks. At the time of recruitment, subjects must have no intention of changing their medication or psychotherapy during the study duration
  9. Any suicidal behavior in the past 1 year (i.e. actual attempt, interrupted attempt, aborted attempt, or preparatory acts or behavior) prior to screening and during the screening period
  10. Recent initiation (within the past 3 months) of cognitive-behavioral therapy or any evidence-based PTSD psychotherapy (Cognitive Processing Therapy [CPT], Prolonged Exposure [PE], Eye Movement Desensitization and Reprocessing [EMDR]); continuation of established maintenance supportive therapy will be permitted
  11. Any history of brain surgery, of penetrating, neurovascular, infectious, or other major brain injury, of epilepsy, or of other major neurological abnormality (including a history of traumatic brain injury [TBI] with loss of consciousness for more than 24 hours or posttraumatic amnesia for more than 7 days)
  12. Any unstable medical condition, as per the clinical judgement of the investigator
  13. In process of establishing/changing governmental/institutional compensation payments for PTSD symptoms
  14. Enrollment in another clinical study at screening or within 2 months prior to screening, or intended enrollment within the duration of this study
  15. Women who are pregnant, nursing, or who plan to become pregnant while in the trial

Sites / Locations

  • NYU Langone Health
  • Barzilai Medical Center
  • Rambam Health Care Campus
  • Mental Health Center in Be'er Ya'akov
  • Sheba Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment

Arm Description

Subjects diagnosed with PTSD will be recruited from the community and from local clinical programs. All subjects will undergo Prism neurofeedback training.

Outcomes

Primary Outcome Measures

Clinician Administered PTSD Scale (CAPS - 5)
The primary objective of this study is to assess the proportion of subjects who demonstrate clinically meaningful improvement in the Clinician Administered PTSD Scale (CAPS - 5) score from Baseline to the 3 months follow-up visit. Clinically meaningful improvement is defined here as a 6-point reduction or more in the CAPS-5 score.

Secondary Outcome Measures

PCL-5 response rate
To assess the proportion of subjects who demonstrate clinically meaningful improvement in the PTSD Checklist for DSM-5 (PCL-5). Clinically meaningful improvement is defined here as a 10-point reduction or more in the PCL-5 score
ERQ score
Change from baseline to Month 3 visit in ERQ score
PHQ-9 score
Change from baseline to Month 3 visit in PHQ-9 score
Clinical Global Impression (CGI)
Change from baseline to Month 3 visit in CGI score

Full Information

First Posted
May 6, 2021
Last Updated
May 31, 2022
Sponsor
GrayMatters Health Ltd.
search

1. Study Identification

Unique Protocol Identification Number
NCT04891614
Brief Title
The PRISM Pilot Trial for Post-Traumatic Stress Disorder
Official Title
THE PRISM-PTSD PILOT TRIAL (Process-Instructed Self Neuro-Modulation ("Prism") Pilot Trial for Post-Traumatic Stress Disorder)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
November 29, 2020 (Actual)
Primary Completion Date
May 31, 2022 (Actual)
Study Completion Date
June 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
GrayMatters Health Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A Prospective, Single-Arm, Open-Label Pilot Trial, to Assess Safety and Effectiveness of Process-Instructed Self neuro-Modulation ("Prism"), as an Adjunct to Standard of Care, in Subjects with Post-Traumatic Stress Disorder (PTSD)
Detailed Description
Prism is a software device intended for neurofeedback (NF) training (i.e. operant condition based on EEG signals, also known as EEG-biofeedback), to be used in combination with a standard computer and supported EEG hardware. For purposes of this training, information for feedback is derived and processed from several EEG channels. Prism provides visual and/or auditory signals that correspond to the patient's computed EEG signal, which serves as a surrogate indicator of achieving a state of reduced amygdala activity. The study is a Prospective, Single-Arm, Open-Label Pilot Trial, to Assess Safety and Effectiveness of Process-Instructed Self neuro-Modulation ("Prism"), as an Adjunct to Standard of Care, in Subjects with Post-Traumatic Stress Disorder (PTSD). The study population will include subjects diagnosed with Post-Traumatic Stress Disorder (PTSD) from 1 year to 20 years after index trauma. The total expected enrollment is up to 100 subjects in one or more sites. The study's primary objective is to assess the safety and effectiveness of fifteen (15) EEG-NF training sessions using the Prism software in reducing PTSD-related symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-Traumatic Stress Disorder (PTSD)
Keywords
PTSD

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
single-arm, open-label study
Masking
None (Open Label)
Allocation
N/A
Enrollment
87 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Experimental
Arm Description
Subjects diagnosed with PTSD will be recruited from the community and from local clinical programs. All subjects will undergo Prism neurofeedback training.
Intervention Type
Device
Intervention Name(s)
PRISM
Intervention Description
Subjects will complete 15 neurofeedback training sessions delivered twice per week, on non-consecutive days, over 8 consecutive weeks.
Primary Outcome Measure Information:
Title
Clinician Administered PTSD Scale (CAPS - 5)
Description
The primary objective of this study is to assess the proportion of subjects who demonstrate clinically meaningful improvement in the Clinician Administered PTSD Scale (CAPS - 5) score from Baseline to the 3 months follow-up visit. Clinically meaningful improvement is defined here as a 6-point reduction or more in the CAPS-5 score.
Time Frame
Baseline visit (Week 1) and 3 month Follow-up visit
Secondary Outcome Measure Information:
Title
PCL-5 response rate
Description
To assess the proportion of subjects who demonstrate clinically meaningful improvement in the PTSD Checklist for DSM-5 (PCL-5). Clinically meaningful improvement is defined here as a 10-point reduction or more in the PCL-5 score
Time Frame
Baseline visit (Week 1), Post-Intervention Visit (Week 9) and 3 month Follow-up visit
Title
ERQ score
Description
Change from baseline to Month 3 visit in ERQ score
Time Frame
Baseline visit (Week 1), Post-Intervention Visit (Week 9) and 3 month Follow-up visit
Title
PHQ-9 score
Description
Change from baseline to Month 3 visit in PHQ-9 score
Time Frame
Baseline visit (Week 1), Post-Intervention Visit (Week 9) and 3 month Follow-up visit
Title
Clinical Global Impression (CGI)
Description
Change from baseline to Month 3 visit in CGI score
Time Frame
Baseline visit (Week 1), Post-Intervention Visit (Week 9) and 3 month Follow-up visit
Other Pre-specified Outcome Measures:
Title
Abbreviated PCL (APCL)
Description
To assess the change in the score of the abbreviated PCL scale (APCL, assessed weekly during the EFP-NF training period)
Time Frame
through study completion, an average of 8 weeks
Title
learning success of the EFP-based neurofeedback
Description
To quantify the learning success of the EFP-based neurofeedback (namely: learning volitional down-regulation of the Amyg-EFP signal, over time, during the EFP-NF training period)
Time Frame
through study completion, an average of 8 weeks
Title
Patient satisfaction survey
Description
To quantify patient satisfaction from the EFP-NF training using survey
Time Frame
through study completion, an average of 5 month
Title
Remission rate
Description
To assess the Remission rate at post training visit (8-9 weeks) and at the 3 months follow-up visit
Time Frame
Baseline visit (Week 1), Post-Intervention Visit (Week 9) and 3 month Follow-up visit

10. Eligibility

Sex
All
Minimum Age & Unit of Time
22 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ages 22 to 65 Any gender Diagnosis of PTSD, established according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) 1 to 20 years since index trauma Ability to give signed, informed consent Normal or corrected-to-normal vision Normal or corrected to normal hearing Subject is able to adhere to the study schedule Exclusion Criteria: Have completed two or more full courses of trauma-focused therapy in the past (i.e., EMDR, Prolong Exposure Therapy, etc.), eligibility will be deemed upon the clinical judgment of the investigator. Lifetime diagnosis for schizophrenia, schizoaffective disorder, schizophreniform disorder, Bipolar I disorder, or delusional disorder Any mood disorder and anxiety disorder according to DSM-5 (in addition to those described in Exclusion 2) that is the primary focus of treatment in the last 6 months prior to screening, as per the clinical judgment of the investigator Lifetime diagnosis of autism, mental retardation at the discretion of the investigator. Diagnosis of moderate or severe substance use disorder within the last 3 months of screening visit (as defined in DSM-5-substance use disorder) or at screening visit Any prescribed Benzodiazepine which cannot be ceased for the duration of the study (with a washout period of at least 2 weeks prior to the first Prism training session) or which cannot be replaced with short-acting benzodiazepines that are taken only for sleeping during the night Any psychotropic medication other than a stable dose of selective serotonin reuptake inhibitors (SSRIs) or serotonin-norepinephrine reuptake inhibitor (SNRIs) Any change in or initiation of- SSRIs or SNRIs antidepressants within the past 4 weeks. At the time of recruitment, subjects must have no intention of changing their medication or psychotherapy during the study duration Any suicidal behavior in the past 1 year (i.e. actual attempt, interrupted attempt, aborted attempt, or preparatory acts or behavior) prior to screening and during the screening period Recent initiation (within the past 3 months) of cognitive-behavioral therapy or any evidence-based PTSD psychotherapy (Cognitive Processing Therapy [CPT], Prolonged Exposure [PE], Eye Movement Desensitization and Reprocessing [EMDR]); continuation of established maintenance supportive therapy will be permitted Any history of brain surgery, of penetrating, neurovascular, infectious, or other major brain injury, of epilepsy, or of other major neurological abnormality (including a history of traumatic brain injury [TBI] with loss of consciousness for more than 24 hours or posttraumatic amnesia for more than 7 days) Any unstable medical condition, as per the clinical judgement of the investigator In process of establishing/changing governmental/institutional compensation payments for PTSD symptoms Enrollment in another clinical study at screening or within 2 months prior to screening, or intended enrollment within the duration of this study Women who are pregnant, nursing, or who plan to become pregnant while in the trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adar Shani
Organizational Affiliation
GrayMatters Health
Official's Role
Study Director
Facility Information:
Facility Name
NYU Langone Health
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States
Facility Name
Barzilai Medical Center
City
Ashkelon
Country
Israel
Facility Name
Rambam Health Care Campus
City
Haifa
ZIP/Postal Code
3109601
Country
Israel
Facility Name
Mental Health Center in Be'er Ya'akov
City
Ness Ziona
ZIP/Postal Code
70350
Country
Israel
Facility Name
Sheba Medical Center
City
Ramat Gan
ZIP/Postal Code
52621
Country
Israel

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The PRISM Pilot Trial for Post-Traumatic Stress Disorder

We'll reach out to this number within 24 hrs