Attention Bias Modification Treatment for Warzone-Related Posttraumatic Stress Disorder (PTSD)
| Status: | Completed |
|---|---|
| Conditions: | Psychiatric |
| Therapuetic Areas: | Psychiatry / Psychology |
| Healthy: | No |
| Age Range: | 19 - 65 |
| Updated: | 4/21/2016 |
| Start Date: | April 2012 |
| End Date: | December 2014 |
Attention Bias Modification Treatment for Warzone-Related PTSD: A Randomized Clinical Trial Magnetoencephalography Study
Veterans with Posttraumatic Stress Disorder (PTSD) will be randomly assigned to either
Attention Bias Modification Treatment (ABMT) designed to reduce bias toward threat or a
placebo control condition not designed to change attention patterns. Outcome measures will
be PTSD, anxiety, depression, and alexithymia symptoms as measured by standard psychological
interviews and questionnaires. Participants will also be invited to participate in
physiological testing before and after receiving AMBT or placebo to serve as additional
outcome measures and assess brain functioning, heart rate, and muscle tension.
The investigators expect to see significant PTSD symptom reduction in the Attention Bias
Modification Treatment (ABMT) group relative to the placebo control group in which no
symptomatic relief is expected. At the end of the study, if ABMT is shown to be effective,
we will offer active ABMT to those participants randomly assigned to the placebo arm if they
would like to receive the treatment.
Attention Bias Modification Treatment (ABMT) designed to reduce bias toward threat or a
placebo control condition not designed to change attention patterns. Outcome measures will
be PTSD, anxiety, depression, and alexithymia symptoms as measured by standard psychological
interviews and questionnaires. Participants will also be invited to participate in
physiological testing before and after receiving AMBT or placebo to serve as additional
outcome measures and assess brain functioning, heart rate, and muscle tension.
The investigators expect to see significant PTSD symptom reduction in the Attention Bias
Modification Treatment (ABMT) group relative to the placebo control group in which no
symptomatic relief is expected. At the end of the study, if ABMT is shown to be effective,
we will offer active ABMT to those participants randomly assigned to the placebo arm if they
would like to receive the treatment.
Inclusion Criteria:
- Veterans with Posttraumatic Stress Disorder (PTSD) serving in United States Military
after March 20, 2003.
Exclusion Criteria:
- Schizophrenia
- Bipolar Disorder
- Obsessive Compulsive Disorder
- Head Injury with Loss of Consciousness for more than 30 minutes
- Active Alcohol/Substance Dependence in past 6 months
We found this trial at
1
site
Creighton University Creighton University, located in Omaha, Neb., offers a top-ranked education in the Jesuit...
Click here to add this to my saved trials
