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Clinical Trials/NCT03350360
NCT03350360
Completed
Not Applicable

Randomized Clinical Trials of Attention Control Training for PTSD Related to Combat or Interpersonal Violence

Creighton University1 site in 1 country73 target enrollmentNovember 17, 2017
ConditionsPTSD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
PTSD
Sponsor
Creighton University
Enrollment
73
Locations
1
Primary Endpoint
Change in posttraumatic stress disorder (PTSD) symptoms from pre to post test
Status
Completed
Last Updated
3 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
November 17, 2017
End Date
November 17, 2020
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amy Badura Brack

Professor of Psychology

Creighton University

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Change in posttraumatic stress disorder (PTSD) symptoms from pre to post test

Time Frame: 30 minute long administration at both pre and post training to measure change. (repeat assessments are conducted 1 month apart)

Structured diagnostic interview for PTSD

Study Sites (1)

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