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Development of the Neuroimaging Biomarker-based Prediction Model of Anxiety-related Disorders: Effect of Mindfulness-based Cognitive Therapy Using Neuroscience on the Brain

Primary Purpose

Anxiety Depression

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Mindfulness-based cognitive therapy using neuroscience (NMBCT)
Sponsored by
CHA University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety Depression focused on measuring mindfulness-based cognitive therapy, mri, neuroscience

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: over 19 years of age a Beck Depression Inventory score of more than 5 but less than 20 points a Beck Anxiety Inventory score of more than 5 but less than 25 points A person who has been sufficiently explained and understood the contents of clinical trials, and maintains the ability to make a free-will decision Those with normal or normal corrected vision Those without claustrophobic symptoms Right-handed person Those who do not have a family history of psychiatric disease in the first family (parents, children, siblings) Exclusion Criteria: Currently taking psychoactive drugs Those with a history of neurological disease, head trauma with loss of consciousness, or mental retardation (IQ <70) A person who currently requires hospitalization due to a serious physical illness or who has not passed 6 months since discharge Pregnant and lactating women A person who is judged to be at risk of serious suicide or violent behavior in a mental status examination A person who is judged to have severe symptoms or significant decline in reality testing and judgment through a mental status examination by a psychiatrist Foreigners Those who are illiterate in Korean Those who have previously received mindfulness-based cognitive therapy If the researcher judges that the researcher is unsuitable for participation in clinical trials due to other reasons

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    NMBCT intervention

    Waitlist

    Arm Description

    Participants in this arm enter the 8-week NMBCT course immediately after the baseline visit.

    Participants in the waitlist control arm will wait for 8 weeks after the baseline visit, and then will be offered an identical 8-week NMBCT course.

    Outcomes

    Primary Outcome Measures

    Change in GMV measured with sMRI
    Change in gray matter volume (GMV) in mm3 measured with structural MRI (sMRI)
    Change in CT measured with sMRI
    Change in cortical thickness (CT) in mm measured with structural MRI (sMRI)
    Change in SA measured with sMRI
    Change in surface area (SA) in mm2 measured with structural MRI (sMRI)
    Change LGI measured with sMRI
    Change in local gyrification index (LGI), ranged from 0 to 1, measured with structural MRI (sMRI)
    Change in FA measured with DTI
    Change in fractional anisotropy (FA), ranged from 0 to 1, measured with diffusion tensor imaging (DTI) and T1-weighted MR image.
    Change in MD measured with DTI
    Change in mean diffusivity (MD), ranged from 0 to 1, measured with diffusion tensor imaging (DTI) and T1-weighted MR image.
    Change in AD measured with DTI
    Change in axial diffusivity (AD), ranged from 0 to 1, measured with diffusion tensor imaging (DTI) and T1-weighted MR image.
    Change in RD measured with DTI
    Change in radial diffusivity (AD), ranged from 0 to 1, measured with diffusion tensor imaging (DTI) and T1-weighted MR image.
    Change in FC measured with fMRI
    Change in functional connectivity (FC) in resting-state functional MRI (fMRI).

    Secondary Outcome Measures

    The changes in the Korean version of Panic Disorder Severity Scale (PDSS).
    To assess panic symptom changes after the 8th week of treatment using the Korean version of the Panic Disorder Severity Scale (PDSS). The PDSS consists of 7 items coded on a 5-point scale (0-4). The total scores ranged from 0 to 28. The higher the total scores, the higher the panic symptom severity.
    The change in the Korean version of Albany Panic and Phobia Questionnaire (APPQ)
    To assess agoraphobia symptoms changes after the 8th week of treatment, the Korean Albany Panic and Phobia Questionnaire (APPQ) was used. The APPQ contains 27 items coded on a 9-point scale (0-8). And it can be used to assess interoceptive fear (8 items), social phobia (10 items), and agoraphobia (9 items). The higher each subscale's total score, the poorer the phobic symptom.
    The change in the Korean version of the Beck Depression Inventory (BDI)-II
    To assess depressive symptoms changes after the 8th week of treatment, the Beck Depression Inventory (BDI)-II was used. The 21 self-administered items that comprise the BDI-II were scored from a range of 0 to 3, with the maximum score being 63. The higher the total scores, the more severe the depressive symptom.
    The change in the Korean version of the Beck Anxiety Inventory (BAI)
    To assess anxiety symptoms changes after the 8th week of treatment, the Beck Anxiety Inventory (BAI) was used. The 21 self-administered items that comprise the BAI were scored from a range of 0 to 3, with the maximum score being 63. The higher the total scores, the more severe the anxiety symptom.
    The change in the Korean version of the Penn State Worry Questionnaire (PSWQ)
    To assess the frequency, intensity, and uncontrollability of pathological worry symptoms changes after the 8th week of treatment, the Penn State Worry Questionnaire (PSWQ) was used. The 16 self-administered items that comprise the PSWQ were scored from a range of 1 (not at all typical) to 5 (very typical), with the maximum score being 80. The higher the total scores, the more severe the pathological worry symptom.
    The change in the Korean version of the Anxiety Sensitivity Inventory-Revised (ASI-R)
    To assess the trait anxiety sensitivity levels changes after the 8th week of treatment, the Korean version of the Anxiety Sensitivity Inventory-Revised (ASI-R) was used. The 36-item ASI-R consists of (1) fear of respiratory symptoms, (2) publicly observable anxiety reactions, (3) cardiovascular symptoms, and (4) cognitive dyscontrol. Total scores range from 0 to 144. The higher the total scores, the higher the anxiety sensitivity levels.
    The change in the Self-Compassion Scale-Short Form (SCS-SF)
    To assess the changes in self-compassion levels after the 8th week of treatment, the Self-Compassion Scale-Short Form (SCS-SF) was used. The 12-item SCS-SF consists of self-kindness (2 items), self-judgment (2 items), common humanity (2 items), isolation subscales (2 items), mindfulness (2 items), and over-identified (2 items). Total scores range from 12 to 60. The reverse score of the negative subscale items (e.g., self-judgment, isolation, and over-identification) was used to compute total self-compassion scores. The higher the total scores, the higher the self-compassion levels.
    The change in the Concise Measure of Subjective Well-Being (COMOSWB)
    To evaluate the changes in subjective well-being levels after the 8th week of treatment, the Concise Measure of Subjective Well-Being (COMOSWB) was used. The COMOSWB consists of life satisfaction, positive affect, and negative affect. The 9-item was scored from a range of 1 (strongly disagree or never) to 7 (strongly agree or always). Total scores range from 7 to 63. The higher the total scores, the higher the subjective well-being levels.
    The change in the Korean Burnout Syndrome Scale (KBOSS)
    To evaluate the changes in burnout symptoms levels after the 8th week of treatment, the Korean Burnout Syndrome Scale (KBOSS) was used. The 12-item KBOSS consists of exhaustion (4 items), cynicism (4 items), and inefficacy (4 items). The 16-item was scored from a range of 1 (strongly disagree) to 7 (strongly agree), with the maximum score being 84. Total scores range from 12 to 84. The higher the total scores, the more severe the burn-out symptom.
    The change in the Korean version of the Grit Scale
    To evaluate the changes in grit levels after the 8th week of treatment, the Korean version of the Grit Scale was used. The 12-item of the Korean version of the Grit scale was scored from a range of 0 (strongly disagree) to 5 (strongly agree), with the maximum score being 60. The higher the total scores, the higher levels of grit.
    side effects
    To evaluate the side effects through the interview

    Full Information

    First Posted
    February 23, 2023
    Last Updated
    August 24, 2023
    Sponsor
    CHA University
    Collaborators
    National Research Foundation of Korea
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05911412
    Brief Title
    Development of the Neuroimaging Biomarker-based Prediction Model of Anxiety-related Disorders: Effect of Mindfulness-based Cognitive Therapy Using Neuroscience on the Brain
    Official Title
    Development of the Neuroimaging Biomarker-based Prediction Model of Anxiety-related Disorders and Novel Treatment Strategies: Effect of Mindfulness-based Cognitive Therapy Using Neuroscience on the Brain
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2023 (Anticipated)
    Primary Completion Date
    February 28, 2024 (Anticipated)
    Study Completion Date
    December 31, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    CHA University
    Collaborators
    National Research Foundation of Korea

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    The purpose of this study designed a randomized clinical trial is to determine the efficacy of an 8-week mindfulness-based cognitive therapy using neuroscience (NMBCT) to reduce anxiety or depressive symptoms among adult participants with anxiety and depression. The primary object is to assess the effectiveness of NMBCT to change in the structural or functional brain. A secondary objective is to reduce clinical symptom severity.
    Detailed Description
    There are reports that mindfulness-based cognitive therapy (MBCT) techniques in patients with panic disorder or depression promote neuroplasticity changes in the brain, thereby restoring individual vulnerability to anxiety. This clinical study aims to develop a metacognitive task that improves existing MBCT as a new treatment that changes the function of anxiety or depression-specific neural circuits, and to explore neurological mechanisms and treatment-related factors. This study was designed to enroll 64 participants, 32 in the NMBCT intervention and 32 in waitlist. This will allow 20% attrition and the Investigators anticipate 52 participants will complete the study. A sample size of 52 will achieve 80% power, given current effect size (cohen's d = 0.40, alpha = 0.05) estimates per aim. Participants randomized to the NMBCT intervention or waitlist group will complete an 8-week NMBCT program conducted by a trained psychiatrist. The waitlist control group will maintain the blind for a treatment period from the baseline and then implement the NMBCT program on the NMBCT intervention group to those who agree. Study data will be collected at 3 times for two groups: T1=1st week session (baseline); T2=8th week session; T3=6 months after baseline. All participants in the clinical study will undergo a total of two brain MRI tests within two weeks before and after visit 2 (T1, baseline) and visit 3 (T2, post-treatment, 8 weeks later).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Anxiety Depression
    Keywords
    mindfulness-based cognitive therapy, mri, neuroscience

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    64 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    NMBCT intervention
    Arm Type
    Experimental
    Arm Description
    Participants in this arm enter the 8-week NMBCT course immediately after the baseline visit.
    Arm Title
    Waitlist
    Arm Type
    Experimental
    Arm Description
    Participants in the waitlist control arm will wait for 8 weeks after the baseline visit, and then will be offered an identical 8-week NMBCT course.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Mindfulness-based cognitive therapy using neuroscience (NMBCT)
    Intervention Description
    Mindfulness-based cognitive therapy using neuroscience (NMBCT) is a standardized 8-week course taught by trained instructors. The NMBCT is a group therapy that takes place once a week for about 90 minutes per session. The program consists of mental education for each session, 2-3 mindfulness meditation practice, mindfulness practice in daily life, and about 30 minutes of daily home mindfulness meditation task. While participating in the program, the subjects will receive psychoeducation and various mindfulness meditation techniques (eating meditation, breathing meditation, sedentary meditation, viewing meditation, and listening meditation, etc.).
    Primary Outcome Measure Information:
    Title
    Change in GMV measured with sMRI
    Description
    Change in gray matter volume (GMV) in mm3 measured with structural MRI (sMRI)
    Time Frame
    baseline, 8 weeks after treatment
    Title
    Change in CT measured with sMRI
    Description
    Change in cortical thickness (CT) in mm measured with structural MRI (sMRI)
    Time Frame
    baseline, 8 weeks after treatment
    Title
    Change in SA measured with sMRI
    Description
    Change in surface area (SA) in mm2 measured with structural MRI (sMRI)
    Time Frame
    baseline, 8 weeks after treatment
    Title
    Change LGI measured with sMRI
    Description
    Change in local gyrification index (LGI), ranged from 0 to 1, measured with structural MRI (sMRI)
    Time Frame
    baseline, 8 weeks after treatment
    Title
    Change in FA measured with DTI
    Description
    Change in fractional anisotropy (FA), ranged from 0 to 1, measured with diffusion tensor imaging (DTI) and T1-weighted MR image.
    Time Frame
    baseline, 8 weeks after treatment
    Title
    Change in MD measured with DTI
    Description
    Change in mean diffusivity (MD), ranged from 0 to 1, measured with diffusion tensor imaging (DTI) and T1-weighted MR image.
    Time Frame
    baseline, 8 weeks after treatment
    Title
    Change in AD measured with DTI
    Description
    Change in axial diffusivity (AD), ranged from 0 to 1, measured with diffusion tensor imaging (DTI) and T1-weighted MR image.
    Time Frame
    baseline, 8 weeks after treatment
    Title
    Change in RD measured with DTI
    Description
    Change in radial diffusivity (AD), ranged from 0 to 1, measured with diffusion tensor imaging (DTI) and T1-weighted MR image.
    Time Frame
    baseline, 8 weeks after treatment
    Title
    Change in FC measured with fMRI
    Description
    Change in functional connectivity (FC) in resting-state functional MRI (fMRI).
    Time Frame
    baseline, 8 weeks after treatment
    Secondary Outcome Measure Information:
    Title
    The changes in the Korean version of Panic Disorder Severity Scale (PDSS).
    Description
    To assess panic symptom changes after the 8th week of treatment using the Korean version of the Panic Disorder Severity Scale (PDSS). The PDSS consists of 7 items coded on a 5-point scale (0-4). The total scores ranged from 0 to 28. The higher the total scores, the higher the panic symptom severity.
    Time Frame
    baseline, 8 week after treatment
    Title
    The change in the Korean version of Albany Panic and Phobia Questionnaire (APPQ)
    Description
    To assess agoraphobia symptoms changes after the 8th week of treatment, the Korean Albany Panic and Phobia Questionnaire (APPQ) was used. The APPQ contains 27 items coded on a 9-point scale (0-8). And it can be used to assess interoceptive fear (8 items), social phobia (10 items), and agoraphobia (9 items). The higher each subscale's total score, the poorer the phobic symptom.
    Time Frame
    baseline, 8 week after treatment
    Title
    The change in the Korean version of the Beck Depression Inventory (BDI)-II
    Description
    To assess depressive symptoms changes after the 8th week of treatment, the Beck Depression Inventory (BDI)-II was used. The 21 self-administered items that comprise the BDI-II were scored from a range of 0 to 3, with the maximum score being 63. The higher the total scores, the more severe the depressive symptom.
    Time Frame
    baseline, 8 week after treatment
    Title
    The change in the Korean version of the Beck Anxiety Inventory (BAI)
    Description
    To assess anxiety symptoms changes after the 8th week of treatment, the Beck Anxiety Inventory (BAI) was used. The 21 self-administered items that comprise the BAI were scored from a range of 0 to 3, with the maximum score being 63. The higher the total scores, the more severe the anxiety symptom.
    Time Frame
    baseline, 8 week after treatment
    Title
    The change in the Korean version of the Penn State Worry Questionnaire (PSWQ)
    Description
    To assess the frequency, intensity, and uncontrollability of pathological worry symptoms changes after the 8th week of treatment, the Penn State Worry Questionnaire (PSWQ) was used. The 16 self-administered items that comprise the PSWQ were scored from a range of 1 (not at all typical) to 5 (very typical), with the maximum score being 80. The higher the total scores, the more severe the pathological worry symptom.
    Time Frame
    baseline, 8 week after treatment
    Title
    The change in the Korean version of the Anxiety Sensitivity Inventory-Revised (ASI-R)
    Description
    To assess the trait anxiety sensitivity levels changes after the 8th week of treatment, the Korean version of the Anxiety Sensitivity Inventory-Revised (ASI-R) was used. The 36-item ASI-R consists of (1) fear of respiratory symptoms, (2) publicly observable anxiety reactions, (3) cardiovascular symptoms, and (4) cognitive dyscontrol. Total scores range from 0 to 144. The higher the total scores, the higher the anxiety sensitivity levels.
    Time Frame
    baseline, 8 week after treatment
    Title
    The change in the Self-Compassion Scale-Short Form (SCS-SF)
    Description
    To assess the changes in self-compassion levels after the 8th week of treatment, the Self-Compassion Scale-Short Form (SCS-SF) was used. The 12-item SCS-SF consists of self-kindness (2 items), self-judgment (2 items), common humanity (2 items), isolation subscales (2 items), mindfulness (2 items), and over-identified (2 items). Total scores range from 12 to 60. The reverse score of the negative subscale items (e.g., self-judgment, isolation, and over-identification) was used to compute total self-compassion scores. The higher the total scores, the higher the self-compassion levels.
    Time Frame
    baseline, 8 week after treatment
    Title
    The change in the Concise Measure of Subjective Well-Being (COMOSWB)
    Description
    To evaluate the changes in subjective well-being levels after the 8th week of treatment, the Concise Measure of Subjective Well-Being (COMOSWB) was used. The COMOSWB consists of life satisfaction, positive affect, and negative affect. The 9-item was scored from a range of 1 (strongly disagree or never) to 7 (strongly agree or always). Total scores range from 7 to 63. The higher the total scores, the higher the subjective well-being levels.
    Time Frame
    baseline, 8 week after treatment
    Title
    The change in the Korean Burnout Syndrome Scale (KBOSS)
    Description
    To evaluate the changes in burnout symptoms levels after the 8th week of treatment, the Korean Burnout Syndrome Scale (KBOSS) was used. The 12-item KBOSS consists of exhaustion (4 items), cynicism (4 items), and inefficacy (4 items). The 16-item was scored from a range of 1 (strongly disagree) to 7 (strongly agree), with the maximum score being 84. Total scores range from 12 to 84. The higher the total scores, the more severe the burn-out symptom.
    Time Frame
    baseline, 8 week after treatment
    Title
    The change in the Korean version of the Grit Scale
    Description
    To evaluate the changes in grit levels after the 8th week of treatment, the Korean version of the Grit Scale was used. The 12-item of the Korean version of the Grit scale was scored from a range of 0 (strongly disagree) to 5 (strongly agree), with the maximum score being 60. The higher the total scores, the higher levels of grit.
    Time Frame
    baseline, 8 week after treatment
    Title
    side effects
    Description
    To evaluate the side effects through the interview
    Time Frame
    baseline, 2 week/4 week/8 week after treatment

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    19 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: over 19 years of age a Beck Depression Inventory score of more than 5 but less than 20 points a Beck Anxiety Inventory score of more than 5 but less than 25 points A person who has been sufficiently explained and understood the contents of clinical trials, and maintains the ability to make a free-will decision Those with normal or normal corrected vision Those without claustrophobic symptoms Right-handed person Those who do not have a family history of psychiatric disease in the first family (parents, children, siblings) Exclusion Criteria: Currently taking psychoactive drugs Those with a history of neurological disease, head trauma with loss of consciousness, or mental retardation (IQ <70) A person who currently requires hospitalization due to a serious physical illness or who has not passed 6 months since discharge Pregnant and lactating women A person who is judged to be at risk of serious suicide or violent behavior in a mental status examination A person who is judged to have severe symptoms or significant decline in reality testing and judgment through a mental status examination by a psychiatrist Foreigners Those who are illiterate in Korean Those who have previously received mindfulness-based cognitive therapy If the researcher judges that the researcher is unsuitable for participation in clinical trials due to other reasons
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Hyun-Ju Kim, MD., PhD
    Phone
    82+31-780-5874
    Email
    guswn10ve@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Hye-Yeon Jung, MA
    Email
    hychung980607@gmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Sang-Hyuk Lee, MD., PhD
    Organizational Affiliation
    Professor at Bundang CHA medical center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Development of the Neuroimaging Biomarker-based Prediction Model of Anxiety-related Disorders: Effect of Mindfulness-based Cognitive Therapy Using Neuroscience on the Brain

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