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
About this trial
This is an interventional supportive care trial for Bipolar Disorder
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
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
NCT ID
NCT02843282
First Posted
July 14, 2016
Last Updated
November 2, 2022
Sponsor
The University of Texas at Dallas
Collaborators
University of Texas
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
Learn more about this trial
Reasoning Training in Individuals With Bipolar Disorder
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