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Clinical Trial Summary

Use of the Fischer Wallace Cranial Stimulator to relieve symptoms related to PTSD.


Clinical Trial Description

The advent of an appreciation that alternative and complementary practices can have some beneficial effect on health has prompted the question of whether there are empirical measures of improvement that do not rely solely on subjective reports. The present study proposes to explore whether transcranial stimulation (or cranial electrotherapy stimulation; CES) using an FDA-approved device can alter brain function, mood and responses to cognitive tasks in patients diagnosed with Post Traumatic Stress Disorder (PTSD). Furthermore, the study will test whether such changes parallel clinical improvement in signs and symptoms. The dependent variables of interest will be magnetic resonance imaging (MRI). Secondarily, we will assess the effects of CES on brain chemistry through the use of magnetic resonance spectroscopy procedures in normal, healthy control participants. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01860677
Study type Interventional
Source Mclean Hospital
Contact
Status Recruiting
Phase N/A
Start date May 2010
Completion date May 2015