Neuromodulation and Neurorehabilitation for mTBI Plus PTSD
Status: | Recruiting |
---|---|
Conditions: | Neurology, Neurology, Psychiatric, Psychiatric |
Therapuetic Areas: | Neurology, Psychiatry / Psychology |
Healthy: | No |
Age Range: | 18 - 60 |
Updated: | 3/15/2019 |
Start Date: | March 2019 |
End Date: | March 2024 |
Contact: | Catherine M Kestner |
Email: | Catherine.Kestner@va.gov |
Phone: | 708-878-0578 |
Neuromodulation and Neurorehabilitation for Treatment of Functional Deficits After mTBI and PTSD
This study will determine (i) the magnitude of immediate and sustained effects of a current
clinical standard interactive computer attention processing training (APT) when combined with
intermittent theta burst stimulation (iTBS), a type of repetitive transcranial magnetic
stimulation and (ii) determine how APT + iTBS changes the neurocognitive system of attention
in individuals with persistent attention deficits related to mTBI and PTSD.
clinical standard interactive computer attention processing training (APT) when combined with
intermittent theta burst stimulation (iTBS), a type of repetitive transcranial magnetic
stimulation and (ii) determine how APT + iTBS changes the neurocognitive system of attention
in individuals with persistent attention deficits related to mTBI and PTSD.
Inclusion Criteria:
- At least 18 years of age and no older than 60 years of age
- 3 months to 10 years post exposure to mTBI event
- Have co-occurring mTBI and PTSD as defined by the Symptom Attribution and
Classification Algorithm (SACA) and the Clinically Administered PTSD Scale for DSM-V
(CAPS-5)
Exclusion Criteria:
- Participating in another research study
- Non-fluent in English (speaking and reading)
- History of epilepsy pre-injury
- Receiving antiepileptic treatment for documented active seizures in the past 6 months
- Taking medications that lower seizure threshold including antipsychotics, buproprion,
trazodone and tramadol
- History of surgery on blood vessels in brain and/or valves of the heart
- History of brain hemorrhage, neurovascular conditions and neurodegenerative disorders
- History or current diagnosis of psychotic spectrum disorders (i.e. bipolar,
schizophrenia)
- Significant heart disease as determined by physician review of medical chart
- Pregnant at time of enrollment or any time during study participation
- MRI or TMS/iTBS contraindications such as claustrophobia, metal in eyes/face or brain
- Cardiac pacemakers/defibrillators, cochlear implants, nerve stimulators, intracranial
metal clips
- Diagnosis of moderate or severe TBI (loss of consciousness > 30 minutes, alteration of
consciousness > 24 hours, post traumatic amnesia or neuropsychological testing results
- Mental health medications have been altered within the month preceding study screening
- Taking prescribed CNS stimulants and choosing to not stop these medications during
study participation
- Testing positive for opiates and do not have a prescription for opiates. If on
prescription opiates and taking more than the equivalent of 200 mg of morphine per
day.
- Taking tricyclic antidepressants
- Questionably valid test performance as indicated by a score of ≤ 85% on the Immediate
Recognition, Delayed Recognition or Consistency Scales of the Medical Symptom Validity
Test (MSVT) and clinical determination of questionable performance validity by a
neuropsychologist on the research team
- Actively suicidal as evidenced by plan to harm or recent attempt communicated on the
Structured Clinical Interview for DSM-V (SCID-5).
- Increased Intracranial Pressure (ICP) as evidenced through a funduscopic evaluation or
on the baseline MRI scan.
- Moderate or severe cannabis use disorder defined by ≥ 4 symptoms on the SCID-5
- Severe alcohol use disorder defined by ≥ 4 symptoms on the SCID-5
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