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A Trial of Cognitive Training in Euthymic Bipolar Disorder

Not Applicable
Withdrawn
Conditions
Bipolar Disorder
Interventions
Behavioral: Working memory training
Registration Number
NCT02476331
Lead Sponsor
University of Calgary
Brief Summary

Bipolar disorder (BD) is characterized by extreme changes in mood and emotion dysregulation. Mood changes are episodic in nature, with distinct periods of mania, depression, and asymptomatic periods of euthymia. In addition to impairments in mood, cognitive impairments are a common feature of the disorder. These cognitive impairments persist during periods of euthymia and are associated with negative clinical and psychosocial outcomes. Specifically, individuals with BD show impairments in executive functions. Recent studies show that emotion regulation can be down-regulated by taxing executive functions, and it can be improved with working memory training, a specific component of executive functions. These initial studies show that emotion regulation is under executive control in healthy individuals; however, the nature of this relationship is not well understood in populations that are affected by impairments in both executive control and emotion regulation. Previous work on cognitive training has not targeted specific cognitive domains with an emphasis on understanding the underlying mechanisms that promote change. Moreover, well-controlled randomized control trial (RCT) studies are needed in order to provide high quality evidence to inform the efficacy of cognitive training interventions for psychiatric populations. The aim of the proposed study is to use a commercially available cognitive training program to study the effects of working memory training on cognitive, clinical, and psychosocial outcomes in patients with BD. We hypothesize that training working memory will lead to improvements in cognitive and emotional functioning, leading to downstream changes that will positively impact untrained outcomes, such as mood and community functioning.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Male or female
  • Age between 18 and 65 years
  • Clinically diagnosed with bipolar disorder I or bipolar disorder II and currently in a euthymic state
  • Normal, or corrected to normal, vision and hearing
  • Able to provide informed consent
Exclusion Criteria
  • Meeting Diagnostic and Statistical Manual 5th edition (DSM-5) diagnostic criteria for a current major depressive episode, manic episode, or hypomanic episode
  • Past electroconvulsive therapy (ECT)
  • Past Transcranial Magnetic Stimulation therapy (TMS)
  • Past 3 month history of substance abuse
  • Diagnosed with a medical condition known to affect cognition (e.g., endocrine disease)
  • Score less than 70 on the Wechsler Abbreviated Scale of Intelligence (WASI)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cognitive trainingWorking memory trainingThe neurocognitive training program will be provided by an online platform called BrainGymmer (https://www.braingymmer.com/en/brain-games/). The experimental group will complete the working memory training, which involves three games: N-back, Multi-Memory, and Moving Memory. These games are designed to engage processes involving updating and manipulation of information. All of the training games provided by BrainGymmer are adaptive, meaning that the level of difficulty increases as users develop expertise on a given task. Participants randomized to the cognitive training arm will complete the training games for 30 minutes per day, 5 days a week, for a total of 10 weeks.
Primary Outcome Measures
NameTimeMethod
Working memory capacityChange from baseline to post-assessment (after 10 weeks of training)

Measured with the Automated Operation Span task (AOSPAN), Wechsler Adult Intelligence Scale (WAIS-IV) Digit Span and Maintenance and Manipulation task

Fluid intelligenceChange from baseline to post-assessment (after 10 weeks of training)

Measured with the Raven's Progressive Matrices (RPM) task

Emotion regulationChange from baseline to post-assessment (after 10 weeks of training)

Measured with the Emotional Stroop task and Emotional N-back task

Secondary Outcome Measures
NameTimeMethod
Depression symptom severityChange from baseline to post-assessment (after 10 weeks of training)

Measured with the 17-item Hamilton Rating Scale for Depression (HRDS-17)

Manic symptom severityChange from baseline to post-assessment (after 10 weeks of training)

Measured with the Young Mania Rating Scale (YMRS)

Community functioningChange from baseline to post-assessment (after 10 weeks of training)

Measured with the Functioning Assessment Short Test (FAST)

Trial Locations

Locations (1)

Foothills Medical Centre

🇨🇦

Calgary, Alberta, Canada

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