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Completed

NCT Number: NCT02843282

Reasoning Training in Individuals With Bipolar Disorder

The purpose of this study is to examine cognitive and brain changes in individuals with bipolar disorder as a result of a cognitive training intervention.

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Key information

Age range

20 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Participants will only include people who are fluent speakers of English, as not all of the standardized and experimental cognitive tests have been normed for non-English speakers. Participants will be screened for significant medical, neurological, or psychiatric illness other than bipolar disorder.

Participants will complete baseline cognitive testing. Reasoning training will take place in small groups, once a week for 2hr/session. After the training, participants will complete the cognitive testing again. A subset of participants who qualify for the brain imaging component will also complete a pre-post resting state brain scan.

Training effects will be measured behaviorally in trained areas (reasoning & physical) and untrained cognitive areas. Additionally, structural and functional brain imaging will measure changes in cerebral blood flow, global and regional brain volume, white matter tracts, efficiency, activation patterns, and blood oxygenation with a particular focus on changes to frontal regions.

Screening Session: A research assistant will conduct screening procedures over the phone including a brief medical questionnaire covering their history, current medications and any pre-existing conditions. Prior diagnosis of bipolar disorder and euthymic state will be confirmed with participant's psychiatrist or treating physician.

Neurocognitive Testing Session: A clinician will administer a group of standardized and experimental tests to each participant for each of the cognitive testing sessions. This session may last up to 3 hours, depending on the pace of the participant's response times. The intent of the tasks is to assess higher level thinking skills, working memory, and selective learning.

Functional magnetic resonance imaging (fMRI): Participants will have fMRI, at each aforementioned time point in the study, during which they will lie in the scanner while images of their brain will be recorded. Each session will take up to 90 minutes. During the fMRI and during the diffusion tensor imaging (DTI) the patient will be asked just to lie still.

Cognitive reasoning training: The gist-based reasoning training will be delivered in one, two hour session each week over 4 weeks. It is strategy-based rather than content-based so that the focus is not content specific or situation-dependent. Gist-based reasoning has been linked to frontal lobe activation and to measures of executive function.

Post Intervention: Following the intervention, patients will repeat the cognitive neuropsychological assessment and fMRI identical to the pre-training assessment. Participants are not paid for any of these tests or training sessions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must have physician or psychiatrist authorization form confirming participant fulfills 4 criteria:
  • has diagnosis of Bipolar I or II
  • has been stable and consistent with medication for last 3 months
  • is in a euthymic, rather than manic or depressive, state
  • is appropriate for a group-based intervention

Exclusion criteria

  • Not a native English speaker
  • Less than 12 years education
  • Additional psychiatric diagnosis

Treatment and study plan

Advanced Reasoning Training

Behavioral

This is a strategy-based intervention to enhance frontal lobe function. Strategies equip participants to improve their strategic attention, integrated reasoning, and innovation abilities.

Other names: Gist Reasoning Training

Primary outcomes

  1. Change From Baseline: Test of Strategic Learning

    Time frame: Pre and within 2 weeks post intervention

    Complex abstraction subtest: After reading a complex text, participants generate a high-level synthesis of abstracted ideas (versus recall of concrete details). [raw scores, min value = 0, max value = 10, higher indicates better performance]

Secondary outcomes

  1. Change From Baseline: Wechsler Adult Intelligence Scale (WAIS), Similarities Subtest

    Time frame: Pre and within 2 weeks post intervention

    Participants are provided with two words/concepts and must state how they are alike; [scaled scores, min value = 0, max value = 19, higher indicates better performance]

  2. Change From Baseline: Delis-Kaplan Executive Function System (DKEFS) Card Sorting

    Time frame: Pre and within 2 weeks post intervention

    Participants must sort a set of cards into as many groups as possible, based on certain parameters. This score reflects the correct number of sorts generated. [scaled scores, min value = 0, max value = 19, higher indicates better performance]

  3. Change From Baseline: Working Memory (Digits Backwards)

    Time frame: Pre and within 2 weeks post intervention

    Participants must recite number sequences in reverse order; [scaled scores, min value = 0, max value = 19, higher indicates better performance]

  4. Change From Baseline: Delis-Kaplan Executive Function System (DKEFS) Color-Word, Inhibition & Switching Subtest

    Time frame: Pre and within 2 weeks post intervention

    Participants must either state color of word or read the word presented; [scaled scores, min value = 0, max value = 19, higher indicates better performance]

  5. Change From Baseline: Divided Attention

    Time frame: Pre and within 2 weeks post intervention

    Participants connect letters and numbers in ascending order as quickly as they can; [raw score in seconds, min value = 0, max value = 200, lower indicates better performance]

  6. Change From Baseline: Verbal Fluency

    Time frame: Pre and within 2 weeks post intervention

    Participants had to generate as many words as possible in one minute that fit task parameters; [scaled scores, min value = 0, max value = 19, higher indicates better performance]

  7. Change From Baseline: Rey Auditory Verbal Learning Test (RAVLT)

    Time frame: Pre and within 2 weeks post intervention

    Participants are asked to recall a list of words they heard 20 minutes earlier; [raw scores, min value = 0, max value = 15, higher indicates better performance]

  8. Change From Baseline: Logical Memory

    Time frame: Pre and within 2 weeks post intervention

    Participants are asked to recall the details of a story they were read 20 minutes earlier; [scaled scores, min value = 0, max value = 19, higher indicates better performance]

  9. Change From Baseline: Quality of Life in Bipolar Disorder (QoL.BD)

    Time frame: Pre and within 2 weeks post intervention

    Participants fill out a self-report questionnaire assessing different domains of quality of life; [raw score; min value = 0, max value = 280, higher score indicates higher reported quality of life]

  10. Resting State Relative Cerebral Brain Blood Flow (rCBF)

    Time frame: Pre (from baseline) and within 2 weeks post intervention

    Mean-level change in resting state relative cerebral brain blood flow (rCBF) in left Inferior frontal gyrus (min value = 0, max value = 2, lower value indicates decreased cerebral blood flow and higher indicates increased cerebral blood flow)

  11. Change From Baseline: Delis-Kaplan Executive Function System (DKEFS) Accurate Description of Sorts

    Time frame: Pre and within 2 weeks post intervention

    Participants must sort a set of cards into as many groups as possible, based on certain parameters, and state why it is an accurate sort. This score reflects the accuracy of the sort description. [scaled scores, min value = 0, max value = 19, higher indicates better performance]

  12. Change From Baseline: Delis-Kaplan Executive Function System (DKEFS) Accurate Recognition of Sorts

    Time frame: Pre and within 2 weeks post intervention

    After proctor has sorted cards, participants must state why sort is accurate/how cards are alike. [scaled scores, min value = 0, max value = 19, higher indicates better performance]

Sponsors and collaborators

Lead sponsor

The University of Texas at Dallas

Other

Collaborators

  • University of Texas

Registry information

Official study title

Brain & Cognitive Changes After Reasoning Training in Individuals With Bipolar Disorder

Important dates

Study start
2014
Primary completion
2015
Study completion
2018
First posted
Jul 25, 2016
Registry last updated
Dec 6, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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