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CCTAP: Cognitive Control Training for Treatment of AUD-PTSD

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Posit Science

Status

Completed

Conditions

Post Traumatic Stress Disorder
Alcohol Use Disorder

Treatments

Other: Computerized Plasticity-Based Adaptive Cognitive Training

Study type

Interventional

Funder types

Industry
Other U.S. Federal agency

Identifiers

NCT03200028
PSC-0613-17

Details and patient eligibility

About

The primary objective of this study is to evaluate the feasibility of the revised brain training program with individuals diagnosed with Alcohol Use Disorder (AUD) and Post-Traumatic Stress Disorder (PTSD).

Enrollment

9 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participant is a Veteran and is enrolled in outpatient Substance Use Disorder treatment within Veteran Affairs Palo Alto Health Care System
  • Participant meets Diagnostic and Statistical Manual of Mental Disorders-5 criteria for current Alcohol Use Disorder and seeking treatment for Alcohol Use Disorder
  • Participant meets Meet Diagnostic and Statistical Manual of Mental Disorders-5 criteria for current PTSD
  • Participant must be willing to perform daily home-based computer exercises for 6 weeks
  • Participant must demonstrate mild cognitive deficit on neuropsychological tests at the screening visit
  • Participant must be a fluent English speaker from the age of 12
  • Participant must have adequate sensorimotor capacity to perform the program, including visual capacity adequate to read from a iPad screen at a normal viewing distance, auditory capacity adequate to understand normal speech, and motor capacity adequate to control a touchpad

Exclusion criteria

  • Participant with diagnosis of an illness or condition with known cognitive consequences (e.g., schizophrenia, bipolar disorder, cancer, multiple sclerosis, Traumatic Brain Injury, mental retardation or pervasive developmental disorder, epilepsy, Parkinson's Disease, delirium or dementia)
  • Participant with active suicidal ideations as measured by the Columbia-Suicide Severity Rating Scale (C-SSRS)
  • Participant with problems performing assessments or comprehending or following spoken instructions
  • Participant who has been treated within 5 years of the date of consent with a computer-based cognitive training program manufactured by Posit Science
  • Participant with current severe traumatic brain injury
  • Participant with any type of dementia
  • Participant with any type of mental retardation
  • Participant with limited ability to speak/read/write/understand English

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

9 participants in 1 patient group

Experimental Treatment
Experimental group
Description:
Computerized plasticity-based adaptive cognitive training requiring a total maximum of 30 treatment sessions, up to 5 sessions per week, 30 minutes per session.
Treatment:
Other: Computerized Plasticity-Based Adaptive Cognitive Training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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