EEG Biofeedback in the Treatment of Chronic Treatment-Resistant PTSD



Status:Archived
Conditions:Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:December 2009
End Date:December 2012

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Application of Neurofeedback as a Mechanism of Affect Regulation Treatment of Adults With Complex Adaptation to Chronic Interpersonal Trauma Exposure


The purpose of this study is to determine whether neurofeedback (NF) training can
significantly reduce the symptoms of Posttraumatic Stress Disorder (PTSD) in individuals
with significant affect dysregulation and chronic, treatment-resistant PTSD. The primary
aims of this study include:

1. To examine whether NF has the potential to significantly reduce symptoms of PTSD.

2. To examine whether NF training can specifically target the area of affect regulation.

3. To examine the mechanism of NF through elucidating the relationship between affect
regulation and PTSD symptom change.


Deficits in affect regulation are associated with a high rate of treatment failure to
well-established evidence-based treatments for Posttraumatic Stress Disorder (PTSD), and
deficits in this domain are most frequently found in individuals with chronic
treatment-resistant PTSD. Aside from one psychological treatment intervention for adult
female survivors of child sexual abuse, no published study has targeted improving affect
regulation in treatment refractory PTSD. The aim of this study is to test and refine EEG
neurofeedback (NF) as an effective treatment for PTSD associated with high levels of affect
dysregulation. We believe improved affect regulation will lead to an overall improvement in
functioning by addressing deficits in executive functioning in PTSD.

Primary Aim: The primary goal of the research is to refine and evaluate NF training for
adults with treatment-resistant PTSD, specifically targeting the domain of affect
regulation. We will evaluate the following questions:

1. Will NF decrease chronic PTSD symptoms in a treatment-resistant sample of adults with
childhood onset PTSD, as measured with the CAPS and the DTS? Hypothesis 1: Subjects in
the active treatment condition will show significantly greater decreases on the CAPS
and DTS than subjects in the placebo condition.

2. Will NF improve affect regulation, as measured by the IASC? Hypothesis 2: Subjects in
the active treatment condition will show significantly greater improvement on the
affect dysregulation subscale of the IASC than individuals in the placebo condition.

3. Will affect regulation, as measured by the IASC, mediate the relationship of NF
training and PTSD, as measured with the DTS? Hypothesis 3: The affect dysregulation
subscale of the IASC will significantly mediate the relationship between NF and DTS
scores while DTS scores will not significantly mediate affect dysregulation.


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Brookline, Massachusetts 02446
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