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CABA for Post-Traumatic Stress Disorder (CABA Trial)

N/A
Waitlist Available
Led By Daniel M Storzbach, PhD
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 39 weeks
Awards & highlights

CABA Trial Summary

This trialwill evaluate a new treatment for Veterans with comorbid mTBI & PTSD to reduce symptoms, improve cognitive functioning & quality of life.

Eligible Conditions
  • Post-Traumatic Stress Disorder
  • Traumatic Brain Injury

CABA Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~39 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 39 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in PTSD symptoms from baseline as measured by the Clinician Administered PTSD Scale - 5
Change in PTSD symptoms from baseline as measured by the PTSD Checklist-5
Change in attention and working memory from baseline as measured by the Wechsler Adult Intelligence Scale-4th Edition, Digit Span Subtest
+6 more
Secondary outcome measures
Change in functional impairment from baseline as measured by the Sheehan Disability Scale
Change in global life satisfaction from baseline as measured by the Satisfaction with Life Scale
Change in health related quality of life from baseline as measured by the Neuro-QOL
+3 more

CABA Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: CABAExperimental Treatment1 Intervention
CABA uses Behavioral Activation (BA) to identify meaningful goals and activities while learning cognitive skills to aid in working toward those goals. Early sessions of CABA focus on learning about mTBI, PTSD, and lifestyle skills that can improve thinking abilities and mood. Cognitive skills taught each week include internal and external skills to help manage problems with memory, attention, and regulation of thinking processes. Investigators and patients will spend a part of each session applying the cognitive skills to managing real life situations and getting patients active in the service of personal goals.
Group II: TAUPlacebo Group1 Intervention
Treatment as Usual (TAU) is the usual care that patients would normally receive at the VA. TAU care involves psychotherapy (counseling) provided by a specialist in the treatment of PTSD. Patients will be offered individual appointments with an experienced provider on the PTSD Clinical Team (PCT). Beyond this, the specific approach will be determined by the patient and his/her provider and may include skills for managing PTSD and/or a chance for the patient to "process" his/her traumatic experiences. Additional treatments may be offered to patients, such as group classes and medications. TAU care may also include additional evaluation and/or treatment of mTBI, provided by the usual care offered in Portland or Seattle's respective neuropsychology clinics. Treatment for mTBI includes individual or group sessions, and is based on clinical need.

Find a Location

Who is running the clinical trial?

VA Office of Research and DevelopmentLead Sponsor
1,612 Previous Clinical Trials
3,305,648 Total Patients Enrolled
Daniel M Storzbach, PhDPrincipal InvestigatorVA Portland Health Care System, Portland, OR
1 Previous Clinical Trials
128 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are individuals currently able to join this investigation?

"This trial, which was initially made available on May 4th 2015 and last updated November 28th 2022, is no longer accepting applicants. Nevertheless, there are a plethora of other clinical trials that are currently looking for patients to join their research."

Answered by AI

Could I potentially join this research endeavor?

"This clinical trial is accepting 95 participants that have been diagnosed with post traumatic stress disorder and fall within the ages of 18 to 55."

Answered by AI

Is enrollment open to people of advanced age in this experiment?

"According to the study's requirements, prospective participants must between 18 and 55 years old. There are 104 trials specifically targeting those below 18 while 538 cater to individuals over 65."

Answered by AI

What aims is this medical experiment attempting to achieve?

"This trial's primary goal, to be measured over 39 weeks, is assessing the alteration of attention and working memory from baseline through Wechsler Adult Intelligence Scale-4th Edition Digit Span Subtest. Secondary objectives involve gauging changes in global life satisfaction with Satisfaction with Life Scale; ascertaining mutations in postconcussion symptoms via Rivermead Postconcussive Questionnaire; and evaluating modifications in signs of anxiety using Brief Symptom Inventory."

Answered by AI
~9 spots leftby May 2025