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Attentional Bias Modification in Patients With Posttraumatic Stress Disorder

Effects of Attentional Bias Modification on Attentional Bias and Symptoms of Posttraumatic Stress Disorder

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00764101
Enrollment
80
Registered
2008-10-01
Start date
2008-09-30
Completion date
2010-04-30
Last updated
2011-07-08

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

Conditions

Posttraumatic Stress Disorder

Brief summary

Randomized, placebo-controlled trial of 9 sessions of computerized attentional bias training on attentional bias and on symptoms of Posttraumatic Stress Disorder.

Interventions

computerized training to reduce attentional bias in posttraumatic stress disorder

Sponsors

Leiden University Medical Center
CollaboratorOTHER
ZonMw: The Netherlands Organisation for Health Research and Development
CollaboratorOTHER
PsyQ
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of Posttraumatic Stress Disorder

Exclusion criteria

* Diagnosis of psychosis, drug- or alcohol dependency/abuse; * Unable to fill in questionnaires in Dutch; * Color blindness (Stroop test).

Design outcomes

Primary

MeasureTime frame
Clinician-Administered PTSD Scale (CAPS)End of Trial + 3 week Follow-Up

Secondary

MeasureTime frame
PTSD symptoms (self-report)end of trial + 3wk Follow Up
Attentional Bias (dot-probe test)End of trial + 3wk Follow-up
Emotional Stroop InterferenceEnd of trial + 3wk Follow Up

Countries

Netherlands

Outcome results

None listed

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