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Hyperbaric Oxygen Therapy for Adult Onset Post Traumatic Stress Disorder

Primary Purpose

Ptsd

Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Hyperbaric oxygen-90 minutes exposure to 100% oxygen at 2 ATA, with 5-minute air breaks every 20 minutes
Sponsored by
Assaf-Harofeh Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ptsd

Eligibility Criteria

25 Years - 60 Years (Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult onset PTSD, defined by DSM-V criteria, as a result of combat or a terror- related event.
  • Age 25-60 years, 4-years or more from the traumatic event and failure to improve with at least one line of conventional treatment.

Exclusion Criteria:

  • A history of traumatic brain injury, epilepsy, a brain tumor; skull base fractures or neurosurgery.
  • Severe substance use disorders a current manic episode, psychotic disorders or serious suicidal ideation at baseline.
  • Major cognitive deficits
  • History of HBOT for any reason, prior to study enrollment.
  • Chest pathology incompatible with pressure changes (including active asthma).
  • Inner ear disease.
  • The inability to perform an awake brain MRI test.
  • Inability to provide informed consent

Sites / Locations

  • Assaf-Harofeh Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

hyperbaric oxygen therapy (HBOT) active treatment

Control-follow up

Arm Description

60 daily HBOT sessions will be administrated 5 days per week. Comprise of 90 minutes exposure to 100% oxygen at 2 ATA, with 5-minute air breaks every 20 minutes.

The standard of care of psychological and mediational support . After 3 months of follow up, participants will be re-evaluated. The individuals in the control group will then be offered to receive the treatment and to be re-reevaluated after the treatment is over (3 months).

Outcomes

Primary Outcome Measures

Change in PTSD symptoms
Symptoms assessed by the PTSD questionnaire (0-80)

Secondary Outcome Measures

Change in Sleep disorders questionnaire
Medical Outcome Sleep Scale (MOS) (0-100) higher values represent a better outcome
Change in Cognitive function
mainstreams Cognitive Health Assessment (values normalized for age and gender, with mean value of 100 and standard deviation of 15)
Change in Brain imaging
Brain imaging will include 2 types of imaging: perfusion magnetic resonance imaging (MRI) + diffusion tensor imaging (DTI), including resting state functional MRI and brain single photon emission computed tomography (PET-CT).
change in symptoms assessed by Diary for daily documentation of symptoms
VAS based mood score higher values represent a worse outcome
Change in Physiological evaluation of brain functionality
This examination includes non-invasive safe brain monitoring and stimulation for the assessment of changes in brain functionality and connectivity. The procedure includes placement of EEG electrodes on an individual's head and measurement of the TMS-evoked electrophysiological response in the various brain regions.

Full Information

First Posted
March 4, 2018
Last Updated
December 1, 2019
Sponsor
Assaf-Harofeh Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03466554
Brief Title
Hyperbaric Oxygen Therapy for Adult Onset Post Traumatic Stress Disorder
Official Title
Hyperbaric Oxygen Therapy for Adult Onset Post Traumatic Stress Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Completed
Study Start Date
March 4, 2018 (Actual)
Primary Completion Date
August 31, 2019 (Actual)
Study Completion Date
September 20, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Assaf-Harofeh Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Posttraumatic stress disorder (PTSD) is the long term effect of severely distressing traumatic event characterized by intrusive thoughts, nightmares, and avoidance. Brain imaging of PTSD patients demonstrate alterations in regional brain perfusion, with stunned, hypoperfused regions. Those brain-biological pathologies may be responsible for the limited success rate of currently available interventions. During the last years data regarding Hyperbaric Oxygen Therapy (HBOT) induced neuroplasticity accumulated. A number of studies in traumatic brain injury, cerebrovascular attacks, and fibromyalgia have presented evidence of improved perfusion and recovery of metabolic brain tissues, accompanied by clinical improvement under HBOT even years after the acute insults. Considerable evidence supports potential benefit of HBOT on PTSD, however, no clinical trial was done on this pure PTSD population. The aim of the proposed study is to examine hyperbaric oxygen therapy as a treatment for PTSD. Advanced brain imaging and functional analysis tools will be used to evaluate treatment's effect.
Detailed Description
Posttraumatic stress disorder (PTSD) has been described as "the complex somatic, cognitive, affective, and behavioral effects of psychological trauma". PTSD is triggered by a severe distressing traumatic event, in which an overwhelming amount of stress exceeds the ability of the individual to cope or integrate the emotions involved in the experience. The fact that a large portion of the affected population is previously healthy, young people who were thrown off their life course, contribute to the great motivation for research in this field. But unfortunately, the current available treatment improve some of the symptoms in only 32-66% of patients, and even after treatment, up to 60% still meet PTSD diagnosis. In the last few years, there is growing knowledge regarding the neuro-biological changes that characterize PTSD. Brain imaging demonstrates alterations in regional brain perfusion, with stunning, hypoperfused regions. Those enduring brain-biological pathologies may explain the limited success rate of currently available interventions. Accumulating studies presents evidence that hyperbaric oxygen therapy (HBOT) can induce neuroplasticity and recovery of metabolic injured brain tissues, even years after the acute insults. HBOT can initiate several brain-repair related mechanisms including brain angiogenesis; improve cerebral vascular flow enable regeneration of axonal white matter, stimulate axonal growth, promote blood-brain barrier integrity and reduce inflammatory reactions, as well as in brain edema. The potential beneficial effects of HBOT were demonstrated in several clinical trials of traumatic brain injury(TBI)/post-concussion patients. Some of these trials, especially those in veterans, included patients who, in addition to post-concussion syndrome, had PTSD; as it is estimated that half of the soldiers with post-concussion syndrome due to mild TBI also meet the criteria of PTSD. The aim of the proposed study is to evaluate the effect of HBOT on PTSD symptoms in adults with treatment resistant PTSD who were not exposed to TBI or blast injury. In addition to the clinical outcome, brain functionality and microstructure will also be evaluated by PET and DTI-MRI in order to shed additional light on the pathophysiology of PTSD and its response to treatment. Study protocol: Thirty male patients with adult onset PTSD, defined by DSM-V criteria, as a result of combat or a terror- related event, will be recruited to the study. Further criteria for study inclusion will be: age 25-60 years, 4-years or more from the traumatic event and failure to improve with at least one line of conventional treatment. Study exclusion criteria will be: a history of traumatic brain injury or blast injury, epilepsy, a brain tumor; skull base fractures or neurosurgery, severe substance use disorders, a current manic episode, psychotic disorders or serious suicidal ideation at baseline; or major cognitive deficits; a history of HBOT for any reason prior to study enrollment; chest pathology incompatible with pressure changes (including active asthma); inner ear disease; the inability to perform an awake brain MRI test; and the inability to provide informed consent. After recruitment, participants will be randomized to one of two study groups . A treatment group will proceed to a course of HBOT, while participants in the control group will continue with the current standard of care of psychiatric support and medications. After 3 months of follow up, participants of both groups will be re-evaluated. The individuals in the control group will then be offered to receive the treatment and to be re-reevaluated after the treatment is over (3 months). Further evaluation will be done at 6 and 12 month to evaluate long term effects of the treatment. During the study, all participant will continue with their current medications unless otherwise advise by their treating physician. According to the HBOT protocol, 60 daily HBOT sessions will be administrated 5 days per week. Comprise of 90 minutes exposure to 100% oxygen at 2 ATA, with 5-minute air breaks every 20 minutes. Study end points: Primary end point PTSD symptoms, as assessed by the PTSD questionnaire Secondary end points Sleep disorders questionnaire: Medical Outcome Sleep Scale (MOS) Quality of life and mood questionnaires: Patient global impression of change, SF-36, EQ-5D, SCL51 Diary for daily documentation of symptoms Cognitive function- Cognitive function will be evaluated by the mainstreams Cognitive Health Assessment. Brain imaging Brain imaging will include 2 types of imaging: perfusion magnetic resonance imaging (MRI) + diffusion tensor imaging (DTI), including resting state functional MRI and brain single photon emission computed tomography (PET-CT). 5.1 Perfusion MRI+DTI and Resting state fMRI (rsfMRI) a method of functional brain imaging that can be used to evaluate regional interactions that occur when a participant is not performing an explicit task. This resting brain activity is observed by means of changes in blood flow in the brain, which creates what is referred to as a blood-oxygen-level dependent (BOLD) signal that can be measured using functional MRI (fMRI). +task 5.2 PET CT Physiological evaluation of brain functionality using transcranial magnetic stimulation (TMS)-EEG examination: This examination includes non-invasive safe brain monitoring and stimulation for the assessment of changes in brain functionality and connectivity. The procedure includes placement of EEG electrodes on an individual's head and measurement of the TMS-evoked electrophysiological response in the various brain regions. The examination takes about 30 minutes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ptsd

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
hyperbaric oxygen therapy (HBOT) active treatment
Arm Type
Experimental
Arm Description
60 daily HBOT sessions will be administrated 5 days per week. Comprise of 90 minutes exposure to 100% oxygen at 2 ATA, with 5-minute air breaks every 20 minutes.
Arm Title
Control-follow up
Arm Type
No Intervention
Arm Description
The standard of care of psychological and mediational support . After 3 months of follow up, participants will be re-evaluated. The individuals in the control group will then be offered to receive the treatment and to be re-reevaluated after the treatment is over (3 months).
Intervention Type
Device
Intervention Name(s)
Hyperbaric oxygen-90 minutes exposure to 100% oxygen at 2 ATA, with 5-minute air breaks every 20 minutes
Intervention Description
60 daily HBOT sessions will be administrated 5 days per week. comprise of 90 minutes exposure to 100% oxygen at 2 ATA, with 5-minute air breaks every 20 minutes.
Primary Outcome Measure Information:
Title
Change in PTSD symptoms
Description
Symptoms assessed by the PTSD questionnaire (0-80)
Time Frame
at baseline and after 3 months
Secondary Outcome Measure Information:
Title
Change in Sleep disorders questionnaire
Description
Medical Outcome Sleep Scale (MOS) (0-100) higher values represent a better outcome
Time Frame
at baseline and after 3 months
Title
Change in Cognitive function
Description
mainstreams Cognitive Health Assessment (values normalized for age and gender, with mean value of 100 and standard deviation of 15)
Time Frame
at baseline and after 3 months
Title
Change in Brain imaging
Description
Brain imaging will include 2 types of imaging: perfusion magnetic resonance imaging (MRI) + diffusion tensor imaging (DTI), including resting state functional MRI and brain single photon emission computed tomography (PET-CT).
Time Frame
at baseline and after 3 months
Title
change in symptoms assessed by Diary for daily documentation of symptoms
Description
VAS based mood score higher values represent a worse outcome
Time Frame
at baseline and after 3 months
Title
Change in Physiological evaluation of brain functionality
Description
This examination includes non-invasive safe brain monitoring and stimulation for the assessment of changes in brain functionality and connectivity. The procedure includes placement of EEG electrodes on an individual's head and measurement of the TMS-evoked electrophysiological response in the various brain regions.
Time Frame
at baseline and after 3 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult onset PTSD, defined by DSM-V criteria, as a result of combat or a terror- related event. Age 25-60 years, 4-years or more from the traumatic event and failure to improve with at least one line of conventional treatment. Exclusion Criteria: A history of traumatic brain injury, epilepsy, a brain tumor; skull base fractures or neurosurgery. Severe substance use disorders a current manic episode, psychotic disorders or serious suicidal ideation at baseline. Major cognitive deficits History of HBOT for any reason, prior to study enrollment. Chest pathology incompatible with pressure changes (including active asthma). Inner ear disease. The inability to perform an awake brain MRI test. Inability to provide informed consent
Facility Information:
Facility Name
Assaf-Harofeh Medical Center
City
Zerifin
ZIP/Postal Code
70300
Country
Israel

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Hyperbaric Oxygen Therapy for Adult Onset Post Traumatic Stress Disorder

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