12% of patients suffering from an acute crornary syndrome will develop long lasting anxiety
symptoms. The object of this study is to lessen or prevent these symptoms by the use of
neurofeed back (EEG-NF).
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT01729780
Ages eligible for Study
18 Years to 70 Years
Genders eligible for Study
Accepts Healthy Volunteers
Underwent MRI scan clearance as accustomed in the Tel Aviv medical center.
The participation of a patient, who underwent an insertion of a coronary stent, will be allowed only if the stent maker cleared in writing the stent exposure to a magnetic field of 3 Tesla, and a written consent by the patients' cardiologist was supplied
Patient does not speak Hebrew.
The patient is having chest pain.
History of psychiatric or neurologic condition requiring hospitalization.
All locations for NCT01729780
View full eligibility
Tris trial is registered with FDA with number: NCT01729780. The sponsor of the trial is Tel-Aviv Sourasky Medical Center and it is looking for 150 volunteers for the current phase.
Official trial title: Early EEG-NF Intervention for the Prevention of PTSD in First Time ACS Patients
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