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Reasoning Training in Individuals With Bipolar Disorder

Primary Purpose

Bipolar Disorder, Cognitive Ability, General

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Advanced Reasoning Training
Sponsored by
The University of Texas at Dallas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Bipolar Disorder

Eligibility Criteria

20 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Must have physician or psychiatrist authorization form confirming participant fulfills 4 criteria:

    1. has diagnosis of Bipolar I or II
    2. has been stable and consistent with medication for last 3 months
    3. is in a euthymic, rather than manic or depressive, state
    4. is appropriate for a group-based intervention

      EXCLUSION CRITERIA:

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

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Cognitive training

    Arm Description

    Advanced reasoning training

    Outcomes

    Primary Outcome Measures

    Change from Baseline: Test of Strategic Learning
    Synthesize a complex text, abstract take away messages, answer detail probes.

    Secondary Outcome Measures

    Change from Baseline: Wechsler Adult Intelligence Scale (WAIS), Similarities subtest
    Concept Formation
    Change from Baseline: DKEFS Card Sorting
    Problem Solving & Concept Formation
    Change from Baseline: Digits Backwards
    Working Memory
    Change from Baseline: DKEFS Color-Word
    Inhibition & Switching
    Change from Baseline: Trails B
    Switching
    Change from Baseline: COWAT
    Verbal Fluency
    Change from Baseline: RAVLT
    Memory
    Change from Baseline: Logical Memory
    Memory
    Change from Baseline: Quality of Life in Bipolar Disorder (QoL.BD)
    Quality of Life questionnaire

    Full Information

    First Posted
    July 14, 2016
    Last Updated
    November 2, 2022
    Sponsor
    The University of Texas at Dallas
    Collaborators
    University of Texas
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02843282
    Brief Title
    Reasoning Training in Individuals With Bipolar Disorder
    Official Title
    Brain & Cognitive Changes After Reasoning Training in Individuals With Bipolar Disorder
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    April 2014 (undefined)
    Primary Completion Date
    September 2015 (Actual)
    Study Completion Date
    February 2018 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    The University of Texas at Dallas
    Collaborators
    University of Texas

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    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.
    Detailed Description
    The experiment will be undertaken with the understanding and written consent of each subject. 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. Additionally, two separate neuropsychological cognitive testing and two functional magnetic resonance imaging (fMRI) imaging procedures will be conducted with each participant: one at baseline prior to cognitive training, the second at the end of cognitive training (4 weeks). These testing procedures are explained below. Each participant will receive an appoint card/schedule of appointments to help them keep track of what is expected of them. During the training program participants will make 1 visit per week for 2 hours each over a 4-week period. Prior to cognitive training, participants' baseline gist and detail processing ability, battery of cognitive functions and neuropsychological measures will be obtained with a battery of cognitive measures. Structural and functional brain measures will also be obtained. All measurements will be taken again at the endpoint of training. 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. Given that the participant meets the requirements covered by the phone screen, participants will be asked to complete further screening. 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. The testing will be done at the Center for BrainHealth at 2200 W. Mockingbird Lane, Dallas, Texas. At the cognitive testing session, participants will sign a release form, and clinicians will fax both the release and 'approval form' to the physician. The neuropsychological cognitive test battery will include tests like Delis-Kaplan Executive Function System (DKEFS) Color-Word Interference Test, Delis-Kaplan Executive Function System (DKEFS) Card Sorting Test, Test of Strategic Learning (TOSL), Auditory Selective Learning, Wechsler Memory Scale (WMS-III) Logical Memory Subtest, Verbal Problem Solving, Wechsler Adult Intelligence Scale (WAIS) Similarities Subtest, Rey-Osterrieth Auditory Verbal Learning Test (RAVLT), Trails A, Trails B, the Controlled Order Word Association Test (COWAT), Wechsler Memory Scale (WMS-III) Digits forward and backwards, and Framing task. Functional magnetic resonance imaging (fMRI): On separate days, the 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. Participants may also receive training individually and through online training sessions instead of in a group setting. 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. Potentially, the learned strategies could be applied across a variety of living contexts such as attending lectures, going to the movies, following news stories, planning and carrying out a project, and understanding brochures outlining changes in health care benefits, to name a few. The strategy instruction is hierarchical and dynamically interdependent, with each strategy building upon previous strategies to transform the concrete meaning into abstracted gist-based meanings through reasoning and inference. Constructing meaning at a higher level of abstraction promotes learning which is more efficient and long lasting. The investigators will use neurocognitive tests and fMRI (explained above) before and after the 4-week period to detect any changes in participants' brain and/ or thinking processes. 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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Bipolar Disorder, Cognitive Ability, General

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    27 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Cognitive training
    Arm Type
    Experimental
    Arm Description
    Advanced reasoning training
    Intervention Type
    Behavioral
    Intervention Name(s)
    Advanced Reasoning Training
    Other Intervention Name(s)
    Gist Reasoning Training
    Intervention Description
    This is a strategy-based intervention to enhance frontal lobe function. Strategies equip participants to improve their strategic attention, integrated reasoning, and innovation abilities.
    Primary Outcome Measure Information:
    Title
    Change from Baseline: Test of Strategic Learning
    Description
    Synthesize a complex text, abstract take away messages, answer detail probes.
    Time Frame
    Pre and within 2 weeks post intervention
    Secondary Outcome Measure Information:
    Title
    Change from Baseline: Wechsler Adult Intelligence Scale (WAIS), Similarities subtest
    Description
    Concept Formation
    Time Frame
    Pre and within 2 weeks post intervention
    Title
    Change from Baseline: DKEFS Card Sorting
    Description
    Problem Solving & Concept Formation
    Time Frame
    Pre and within 2 weeks post intervention
    Title
    Change from Baseline: Digits Backwards
    Description
    Working Memory
    Time Frame
    Pre and within 2 weeks post intervention
    Title
    Change from Baseline: DKEFS Color-Word
    Description
    Inhibition & Switching
    Time Frame
    Pre and within 2 weeks post intervention
    Title
    Change from Baseline: Trails B
    Description
    Switching
    Time Frame
    Pre and within 2 weeks post intervention
    Title
    Change from Baseline: COWAT
    Description
    Verbal Fluency
    Time Frame
    Pre and within 2 weeks post intervention
    Title
    Change from Baseline: RAVLT
    Description
    Memory
    Time Frame
    Pre and within 2 weeks post intervention
    Title
    Change from Baseline: Logical Memory
    Description
    Memory
    Time Frame
    Pre and within 2 weeks post intervention
    Title
    Change from Baseline: Quality of Life in Bipolar Disorder (QoL.BD)
    Description
    Quality of Life questionnaire
    Time Frame
    Pre and within 2 weeks post intervention

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    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
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Sandra Chapman, PhD
    Organizational Affiliation
    University of Texas at Dallas
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    Not at this time
    Citations:
    PubMed Identifier
    26070195
    Citation
    Demant KM, Vinberg M, Kessing LV, Miskowiak KW. Effects of Short-Term Cognitive Remediation on Cognitive Dysfunction in Partially or Fully Remitted Individuals with Bipolar Disorder: Results of a Randomised Controlled Trial. PLoS One. 2015 Jun 12;10(6):e0127955. doi: 10.1371/journal.pone.0127955. eCollection 2015.
    Results Reference
    background
    PubMed Identifier
    23717272
    Citation
    Preiss M, Shatil E, Cermakova R, Cimermanova D, Ram I. Personalized cognitive training in unipolar and bipolar disorder: a study of cognitive functioning. Front Hum Neurosci. 2013 May 13;7:108. doi: 10.3389/fnhum.2013.00108. eCollection 2013.
    Results Reference
    background
    PubMed Identifier
    19895584
    Citation
    Deckersbach T, Nierenberg AA, Kessler R, Lund HG, Ametrano RM, Sachs G, Rauch SL, Dougherty D. RESEARCH: Cognitive rehabilitation for bipolar disorder: An open trial for employed patients with residual depressive symptoms. CNS Neurosci Ther. 2010 Oct;16(5):298-307. doi: 10.1111/j.1755-5949.2009.00110.x.
    Results Reference
    background
    PubMed Identifier
    24808834
    Citation
    Chapman SB, Mudar RA. Enhancement of cognitive and neural functions through complex reasoning training: evidence from normal and clinical populations. Front Syst Neurosci. 2014 Apr 28;8:69. doi: 10.3389/fnsys.2014.00069. eCollection 2014.
    Results Reference
    background
    PubMed Identifier
    27847486
    Citation
    Venza EE, Chapman SB, Aslan S, Zientz JE, Tyler DL, Spence JS. Enhancing Executive Function and Neural Health in Bipolar Disorder through Reasoning Training. Front Psychol. 2016 Nov 1;7:1676. doi: 10.3389/fpsyg.2016.01676. eCollection 2016.
    Results Reference
    derived

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    Reasoning Training in Individuals With Bipolar Disorder

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