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CompletedNCT02766296Updated Jun 21, 2018

Emotional Working Memory Training for Veterans With PTSD Symptoms

An interventional study of Active Emotional Working Memory Training and Control Working Memory Training in Posttraumatic Stress Disorder, sponsored by Milwaukee VA Medical Center. Completed at 1 site in United States. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2018-06-21.

Sponsored by Milwaukee VA Medical Center · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
33
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

PTSD is characterized by recurrent intrusion of trauma-related memories and images that cause significant distress and impairment to the affected individuals. The current project aims to examine whether computerized emotional working memory training (eWMT) can help improve working memory capabilities and reduce trauma-related emotional symptoms among individuals with elevated trauma-related symptoms. Participants will be randomly assigned to one of the two computerized training programs. At baseline, post-training, and 1-month follow-up, participants will be assessed with respect to their emotional symptoms and working memory-related cognitive performance. Pending successful outcomes, this study will provide important knowledge that will guide the future efforts to develop an effective, accessible, and cost-efficient intervention program.

Read the detailed description

PTSD is characterized by recurrent intrusion of trauma-related memories and images that cause significant distress and impairment to the affected individuals. The long-term objective is to develop an effective cognitive treatment program that can reduce such intrusive cognitions observed among individuals who have been exposed to a significant trauma. The specific objective is to examine whether computerized emotional working memory training (eWMT) can help improve working memory capabilities and reduce trauma-related emotional symptoms among individuals with elevated trauma-related symptoms. eWMT is designed to improve the individual's ability to stay focused on the target and filter out irrelevant information from their working memory, which is expected to improve trauma-related emotional symptoms via the improvement of working memory functioning.

Individuals who display elevated trauma symptoms will be randomly assigned to one of two eWMT conditions: (a) adjustable n-back training (i.e., potent working memory training program), and (b) fixed 1-back training (i.e., training that delivers a limited dose). Participants will be blinded to ensure objective assessment of the intervention effects. Before and after the eWMT intervention, all participants will undergo an assessment session that aims to assess each individual's emotional symptoms and working memory-related cognitive performance. Further, following completion of procedure, participants will be invited for a follow-up assessment to assess the long-term effect of training.

The eWMT intervention will be delivered via Internet. Thus, the current intervention is a home-based Internet intervention, which provides an important context for testing and developing a cost-efficient, accessible, and effective intervention program for many individuals suffering from exposure to traumas. Each training session will take about 20 minutes, and all participants in both conditions will receive a total of 15 training sessions. Participants will be guided to complete an average of 3 training sessions every week for a total duration of approximately 5 weeks.

Investigators hypothesize that individuals who undergo the active eWMT will display a greater improvement in overall working memory performance and a greater reduction in trauma-related symptoms, compared to individuals who undergo the less effective control training program. Pending successful outcomes, this study will provide important knowledge that will guide the future efforts to develop an effective, accessible, and cost-efficient intervention program that can reach out to many individuals who suffer from exposure to traumas.

02

Conditions studied

  • Posttraumatic Stress Disorder

Keywords

  • PTSD
  • trauma
  • working memory
  • working memory training
03

In context

Stress Disorders, Post-Traumatic

2,239 studies on the registry are indexed under Stress Disorders, Post-Traumatic; 554 are open to participants now.

This study's enrollment of 33 is below the median of 70 across 1,858 interventional studies indexed under Stress Disorders, Post-Traumatic.

Browse Stress Disorders, Post-Traumatic studies →

Lead sponsor

Milwaukee VA Medical Center is the lead sponsor of 3 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Fluently speaks English
  • The PTSD Checklist (PCL-5) total score >= 38

Exclusion criteria

Exclusion Criteria:

  • No access to a private computer with high-speed Internet that can be used privately.
  • Elevated suicidality
  • History of psychotic disorders (e.g., schizophrenia)
  • Severe substance use disorder (as per DSM-5 criteria)
  • History of severe brain injury or organic mental syndrome
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
33 participants (actual)

Study arms

  • Experimental
    Active Emotional Working Memory Training

    Each participant will receive 15 sessions (each lasting 20 minutes) over a 5 week. This will be Internet-based cognitive training based on the adaptive dual n-back paradigm.

    Behavioral: Active Emotional Working Memory Training

  • Placebo comparator
    Control Working Memory Training

    Participants in this condition will receive 15 sessions (each lasting 20 minutes) over a 5-week period. This will also be home-based training over the Internet. This training will be based on a fixed 1-back training program.

    Behavioral: Control Working Memory Training

Interventions

  • BehavioralActive Emotional Working Memory Training

    This training regimen has adapted the existing n-back paradigm, which has been widely used in the field. Training requires participants to shift between visual and auditory information while continually updating their working memory.

  • BehavioralControl Working Memory Training

    This training utilized a fixed dual 1-back training paradigm.

06

What researchers measure

Primary outcomes

  1. Change in Severity of trauma-related symptoms from baseline to post-training and 1-month follow-up

    PTSD Checklist (PCL-5)

    Time frame: At baseline, at post-training (after 5 weeks), and at follow-up (1 month from the completion of training)

Secondary outcomes

  1. Change in working memory performance from baseline to post-training and 1-month follow-up

    Automated Complex Span Tasks (Oswald et al., 2014). This is a well-validated computerized measure of working memory capacity, including three sub-domains: (1) Operation span, (2) Reading span, and (3) Symmetry span.

    Time frame: At baseline, at post-training (after 5 weeks), and at follow-up (1 month from the completion of training)

Other outcomes

  1. Change in physiological reactivity to the description of one's own traumatic experience from baseline to post-training and 1-month follow-up

    Each participant will be guided to listen to the audiotaped version of his/her own traumatic experience while trying to recollect the event as vividly as possible. Raw ECG signals will be recorded before, during, and after the recollection to measure changes in heart rate variability as an index for emotional regulation and physiological reactivity.

    Time frame: At baseline, at post-training (after 5 weeks), and at follow-up (1 month from the completion of training)

07

Study locations

1 site
  • Clement J. Zablocki VA Medical Center
    Milwaukee, Wisconsin 53295, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 21, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02766296
Lead sponsor
Milwaukee VA Medical Center
Responsible party
Sadie Larsen (Assistant Professor, Milwaukee VA Medical Center) — Principal investigator
First posted
May 9, 2016
Start date
May 2016
Primary completion
May 2, 2018
Completion
May 2, 2018
Last update
Jun 21, 2018

Study contacts

Sadie Larsen, Ph.D.
principal investigator · Clement J. Zablocki VA Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2018. You cannot join it, but the record below documents what was studied.

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