Status:

COMPLETED

Attention-Bias Modification Treatment for PTSD

Lead Sponsor:

Research Foundation for Mental Hygiene, Inc.

Conditions:

Posttraumatic Stress Disorder (PTSD)

Eligibility:

All Genders

18-60 years

Phase:

NA

Brief Summary

Emerging research implicates biased attention to threat in the pathophysiology of anxiety disorders. Recent findings demonstrate significant associations between attention bias and stress vulnerabilit...

Detailed Description

ABM is designed to implicitly modify patients' biased threat attendance via computerized training protocols. Emerging evidence indicates that ABM is effective in modifying threat-related attention bia...

Eligibility Criteria

Inclusion

  • Males or females between the ages of 18 and 60;
  • Current DSM-IV PTSD for the last 12 months or more;
  • Fluent in English and willing and able to give informed written consent and participate responsibly in the protocol;
  • Attention bias toward or away from threat assessed by Dot-probe attention bias task

Exclusion

  • Current DSM-IV Axis I disorder other than PTSD.
  • Patients with comorbid (i.e., secondary diagnosis of) major depressive disorder (MDD) will be allowed for enrollment if their HAM-D score doesn't exceed 25;
  • Prior or current diagnosis of schizophrenia, schizoaffective disorder, organic mental disorder, bipolar disorder, or antisocial, schizotypal, and schizoid personality disorders;
  • Suicidal ideation or behavior that poses a significant danger to the subject. Unstable clinical condition such that participation in a controlled trial would pose a significant danger;
  • Prior participation in attention bias modification treatment (ABMT);
  • Current or past history of seizure disorder (except febrile seizure in childhood);
  • Currently on psychotropic medication. (excluding the use of hypnotics);
  • Currently participating in formal psychotherapy. This includes:
  • psychodynamic,
  • cognitive behavioral and interpersonal therapies
  • Current unstable or untreated medical illness;
  • Vision loss.

Key Trial Info

Start Date :

May 1 2013

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 2 2018

Estimated Enrollment :

50 Patients enrolled

Trial Details

Trial ID

NCT01888653

Start Date

May 1 2013

End Date

April 2 2018

Last Update

April 13 2022

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

New York State Psychiatric INstitute

New York, New York, United States, 10032

Attention-Bias Modification Treatment for PTSD | DecenTrialz