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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03350360
Other study ID # 1123259
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 17, 2017
Est. completion date November 17, 2020

Study information

Verified date July 2022
Source Creighton University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Participants will complete a pre and post training psychological assessment. Participants will be assigned to attention control training or the comparison stimuli computer task in a double-blind randomized control trial design. Both computerized dot probe tasks display two stimuli on a computer screen, one above the other, followed by a small right or left arrow appearing in the location vacated by one of the stimuli. Participants are required to respond as quickly as they can by pressing the indicated right or left arrow on their computer keyboard without compromising accuracy. Participants complete 6 training sessions.


Recruitment information / eligibility

Status Completed
Enrollment 73
Est. completion date November 17, 2020
Est. primary completion date November 17, 2020
Accepts healthy volunteers No
Gender All
Age group 19 Years to 80 Years
Eligibility Inclusion Criteria: - military veteran or woman exposed to interpersonal violence (e.g. domestic or sexual violence). - significant symptoms of PTSD Exclusion Criteria: - bipolar disorder, schizophrenia, OCD, unable to attend sessions sober.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Attention Control Training
Attention control training teaches participants that the emotional salience of cues (i.e., threatening or neutral) is not related to successful completion of the computerized response task, and thus, teaches participants to ignore irrelevant threat-related contingencies (Badura-Brack et al., 2015).
Comparison Task
Neutral- neutral stimuli prior to response task

Locations

Country Name City State
United States Creighton University Omaha Nebraska

Sponsors (1)

Lead Sponsor Collaborator
Creighton University

Country where clinical trial is conducted

United States, 

References & Publications (1)

Badura-Brack AS, Naim R, Ryan TJ, Levy O, Abend R, Khanna MM, McDermott TJ, Pine DS, Bar-Haim Y. Effect of Attention Training on Attention Bias Variability and PTSD Symptoms: Randomized Controlled Trials in Israeli and U.S. Combat Veterans. Am J Psychiatry. 2015 Dec;172(12):1233-41. doi: 10.1176/appi.ajp.2015.14121578. Epub 2015 Jul 24. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in posttraumatic stress disorder (PTSD) symptoms from pre to post test Structured diagnostic interview for PTSD 30 minute long administration at both pre and post training to measure change. (repeat assessments are conducted 1 month apart)
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