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Attentional Bias Retraining in Veterans (ABR)

V

VA Pacific Islands Health Care System

Status

Completed

Conditions

Posttraumatic Stress Disorder

Treatments

Behavioral: Attentional bias retraining

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT02041572
2012-05/MM/PROMISE 0001

Details and patient eligibility

About

The study has two goals. First to develop a computer-based intervention meant to alter cognitive biases that contribute to ongoing PTSD symptoms. Second, we sought to pilot test the intervention in a small sample of veterans for feasibility and acceptability.

Full description

Aim 1: Develop Attentional Bias Retraining protocol (Phase 1)

  • 1.1 Computerized assessment & retraining programs
  • 1.2 Procedures and measures

Aim 2: Implement in pilot sample (Phase 2)

  • 2.1: Assess feasibility and tolerability
  • 2.2: Collect pilot data to plan future studies
  • 2.3: Efficacy estimates based on changes in response time to dot probe task

Enrollment

22 patients

Sex

Male

Ages

18 to 89 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participated in ground combat operations in Vietnam
  • Scored 40 - 80 on PTSD Checklist - Military version
  • Availability and willingness to attend 2x weekly computer sessions for 6 weeks

Exclusion criteria

  • Active substance dependence
  • Significant cognitive impairment
  • Current and active suicidal or homicidal ideation

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

22 participants in 1 patient group

Attentional Bias Retraining
Other group
Description:
Each participant receives 12 sessions. The first three sessions are baseline (assessment only) sessions. The last four sessions must be treatment sessions. The attentional bias intervention starts randomly on sessions 4 - 8, and continues until the end of the 12 sessions.
Treatment:
Behavioral: Attentional bias retraining

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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