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Attention Control Training for PTSD Related to Combat or Interpersonal Violence

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03350360
Enrollment
73
Registered
2017-11-22
Start date
2017-11-17
Completion date
2020-11-17
Last updated
2022-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

PTSD

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.

Interventions

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).

BEHAVIORALComparison Task

Neutral- neutral stimuli prior to response task

Sponsors

Creighton University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Masking description

Random assignment and coded entry to a computer website

Eligibility

Sex/Gender
ALL
Age
19 Years to 80 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in posttraumatic stress disorder (PTSD) symptoms from pre to post test30 minute long administration at both pre and post training to measure change. (repeat assessments are conducted 1 month apart)Structured diagnostic interview for PTSD

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026