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Cognitive and Emotion Regulation Training in MS (CERT-MS)

Primary Purpose

Multiple Sclerosis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mindfulness Meditation
Computerized Cognitive Training
Sponsored by
Ohio State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis

Eligibility Criteria

30 Years - 59 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. 30-59 years of age
  2. Score higher than or equal to 23 on the Mini Mental Status Examination (MMSE)
  3. Corrected (near and far) visual acuity of 20/40 or better
  4. No previous experience with mindfulness or continuous meditation practice
  5. Absence of other co-morbid neurological disorders
  6. Relapse free for the last 30 days
  7. No use of corticosteroids for the last 30 days
  8. Clinically definite diagnosis of MS
  9. Ability to use a computer and connect the internet from their home
  10. Generation of at least two worries and two ruminations during the daily diary portion of the study for the pre-assessment session

Exclusion Criteria:

  1. Below 30 years of age or above 59 years of age
  2. Score lower than 23 on the MMSE
  3. Corrected (near or far) visual acuity of 20/40 or greater
  4. Previous experience or participation in a mindfulness program
  5. Presence of co-morbid neurological disorders such as:

    • Alzheimers
    • Parkinson's disease
    • Dementia
  6. Presence of a relapse within the last 30 days
  7. Use of corticosteroids within the last 30 days
  8. Clinically isolated syndrome suggestive of MS
  9. No ability to use a computer and/or a lack of internet connection from their home
  10. No self-generated worries and ruminations in the week-long daily diary portion of the study at pre-assessment

Sites / Locations

  • Department of Psychology, The Ohio State University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

No Intervention

Arm Label

Mindfulness Meditation Training (MMT)

Computerized Cognitive Training

Wait-List Control Group

Arm Description

Participants will attend four weekly group mindfulness meditation sessions of a 2-hour duration. The classes are a mixture of experiential practices, discussions surrounding the experiences, and didactics on mindfulness. In addition to the time spent in session, participants will be asked to complete 40 minutes of daily homework, which includes further practice of in-session meditative exercises and brief readings.

The active control group will be in the form of a cognitive training course where the participants will meet for the same amount of time as the MMT group. Homework will be reading and engaging in cognitive video game exercises for the same duration, around 40 minutes daily, as the MMT group.

This group will be used to compare the effects of the two active comparison groups and will not receive any intervention for the four week period.

Outcomes

Primary Outcome Measures

Change in Reported Engagement After Worry and Rumination Inductions
Participants will engage in worry and rumination inductions during both the pre- and post-intervention sessions. These worries and ruminations will be sampled from the daily diaries participants will fill out 7-days before the pre- and post-intervention sessions. Investigators will be examining the change in emotion and strategy implementation over the course of the worry and rumination inductions. Specifically, investigators will examine the change in reported negative and positive emotion related to the worry and rumination inductions from pre- to post-intervention. Further, investigators will examine the induction-related change in strategy implementation, specifically worry and rumination, over the 4-weeks of intervention.

Secondary Outcome Measures

Cognitive Performance on Brief Repeatable Battery (BRB)
Participants will perform the entire Brief Repeatable Battery before and after the intervention. Using the categorization developed by Sepulcher (2013), the 5 tests of the BRB will be analyzed using four cognitive domains: attention and executive functioning, verbal memory, visual memory, and word fluency. Based on the computerized cognitive training protocol employed in the current study, investigators hypothesize changes in attention and executive functioning along with visual memory in participants in the cognitive training group, followed by participants in the MMT group compared with the wait-list control participants.
Heart Rate Variability (HRV)
HRV data will be collected during worry and rumination inductions, as participants regulate their emotions, and at rest.
Daily Emotion Regulation Diary
Participants will be asked to fill out worry and ruminations using a diary-based methodology a week before the pre-intervention behavioral session and one week after the post-intervention sessions. Changes in average self-reported worry and rumination intensity, emotion regulation strategy use, and successful emotion regulation strategy implementation will be examined as a function of the intervention.
Improvements on a Self-Report Measure of Emotion Dysregulation
Emotion Dysregulation will be assessed using the Difficulties in Emotion Regulation Scale (DERS). Changes on the total score and sub-facets of DERS will be examined as a function of the intervention.
Improvements on a Self-Report Measure of Depression
Participants will be administered Beck Depression Inventory before and after the intervention. Change on this measure will be examined to assess the impact of the interventions on symptoms of depression.
Improvements on a Self-Report Measures of Anxiety
Participants will be administered Penn State Worry Questionnaire before and after the intervention. Change on this measure will be examined to assess the impact of the interventions on symptoms of worry.
Improvements on a Self-Report Measure of Perceived Stress
Participants will be administered the Perceived Stress Scale before and after the intervention. Changes in these measures will be examined as a function of the intervention.
Improvements on a Self-Report Measure of Quality of Life
Participants will be administered the Satisfaction with Life Scale before and after the intervention. Change in scores of this measure will be examined to assess changes in quality of life as a function of the interventions.

Full Information

First Posted
October 21, 2015
Last Updated
April 13, 2018
Sponsor
Ohio State University
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1. Study Identification

Unique Protocol Identification Number
NCT02717429
Brief Title
Cognitive and Emotion Regulation Training in MS
Acronym
CERT-MS
Official Title
Cognitive and Emotion Regulation Training in Multiple Sclerosis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
October 2015 (undefined)
Primary Completion Date
May 14, 2017 (Actual)
Study Completion Date
May 14, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators propose to conduct a randomized feasibility study of mindfulness meditation training (MMT) relative to an active cognitive training control group and waitlist control group in improving emotional regulation in individuals with MS. Individuals will complete pre- and post-assessments of emotional functioning through a week of daily diary entries, as well as self-report measures and a behavioral paradigm. Additionally, all participants will complete an evaluation of neuropsychological functioning, before and after intervention.
Detailed Description
Epidemiological data provides evidence for the manifold increase in rates of depression and anxiety in individuals diagnosed with multiple sclerosis, relative to the general population. Such impaired affective processes, including deficits in emotion regulation have been linked to greater cognitive deficits, a lower quality of life, and greater disease progression in this population. Despite evidence of the deleterious impact of affective functioning on prevalence rates of mood and anxiety disorders; on poor cognitive functioning; and reduced quality of life, much of the targeted intervention research in MS has not directly tested the feasibility, and subsequent efficacy of a psychosocial intervention in improving affective regulation in this population. Thus, the investigators propose to conduct a randomized feasibility study of mindfulness training relative to an active cognitive training control group and waitlist control group in improving emotional regulation in individuals with MS. All individuals that contact the Clinical Neuroscience Laboratory (CNLab) with interest in this study will undergo a phone screening assessing inclusion/exclusion criteria. Those participants meeting I/E criteria will be invited for an online daily diaries portion of the study examining daily engagement in worry and rumination. After completing the week-long daily diary portion of the study, the participant will attend 1-2 in-person pre-assessment sessions, which will also be completed at the completion of the four week intervention. The pre-assessment will involve a thorough assessment of emotion regulation skills, both through self-report questionnaires and behavioral paradigms, and cognitive functioning. Following the assessment sessions, which will be conducted by blind assessors, participants will be randomized to the three groups. The 4-week mindfulness program will be closely modeled after the protocol developed by Dr. Jon Kabat-Zinn, where investigators will have the participants attend once-per-week sessions for 2 hours and complete around 40 minutes a day of homework assignments. The four weeks of mindfulness involve the practice of concentrative attention, where different objects are used as the focus of practices. For example, for the first two weeks, the investigators use breath as an anchor for the mind. With repeated practices, the objects of sensations, emotions, and thought processes are introduced. The classes are a mixture of experiential practices, discussions surrounding the experiences, and didactics on mindfulness. The control group, which will be used to compare the effects of mindfulness training on emotional and cognitive functioning of MS patients, will comprise of a cognitive training group, which will provide an attentional-training based approach. In this group, our focus will be to provide the individuals with cognitive training tasks to complete that have been shown to improve attentional ability. Homework will be reading and practicing using the cognitive video game exercises for the same duration, around 40 minutes daily, as the mindfulness group. Following the four weeks of the intervention, the questionnaires, week-long daily diaries, and behavioral tests from the pretest will be repeated a second time to obtain post-test data for comparison.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mindfulness Meditation Training (MMT)
Arm Type
Experimental
Arm Description
Participants will attend four weekly group mindfulness meditation sessions of a 2-hour duration. The classes are a mixture of experiential practices, discussions surrounding the experiences, and didactics on mindfulness. In addition to the time spent in session, participants will be asked to complete 40 minutes of daily homework, which includes further practice of in-session meditative exercises and brief readings.
Arm Title
Computerized Cognitive Training
Arm Type
Active Comparator
Arm Description
The active control group will be in the form of a cognitive training course where the participants will meet for the same amount of time as the MMT group. Homework will be reading and engaging in cognitive video game exercises for the same duration, around 40 minutes daily, as the MMT group.
Arm Title
Wait-List Control Group
Arm Type
No Intervention
Arm Description
This group will be used to compare the effects of the two active comparison groups and will not receive any intervention for the four week period.
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness Meditation
Intervention Description
The mindfulness meditation-training program is closely modeled after the 8-week mindfulness based stress reduction protocol developed by Dr. Jon Kabat-Zinn. The briefer four weeks of MMT involve the practice of concentrative attention, where different objects are used as the focus of meditative practices. For example, for the first two weeks, the investigators use breath as an anchor for attention. With repeated practices, the objects of sensations, emotions, and thought processes are introduced.
Intervention Type
Behavioral
Intervention Name(s)
Computerized Cognitive Training
Intervention Description
The control group, which will be used to compare the effects of mindfulness training on emotional and cognitive functioning of MS patients, will comprise of a cognitive training group, which will provide an attentional-training based approach. In this group, the focus will be to provide the individuals with cognitive training tasks to complete that have been shown to improve attentional ability. The investigators will also discuss relevant MS-related material on cognitive deficits during these courses.
Primary Outcome Measure Information:
Title
Change in Reported Engagement After Worry and Rumination Inductions
Description
Participants will engage in worry and rumination inductions during both the pre- and post-intervention sessions. These worries and ruminations will be sampled from the daily diaries participants will fill out 7-days before the pre- and post-intervention sessions. Investigators will be examining the change in emotion and strategy implementation over the course of the worry and rumination inductions. Specifically, investigators will examine the change in reported negative and positive emotion related to the worry and rumination inductions from pre- to post-intervention. Further, investigators will examine the induction-related change in strategy implementation, specifically worry and rumination, over the 4-weeks of intervention.
Time Frame
Baseline and 4 weeks
Secondary Outcome Measure Information:
Title
Cognitive Performance on Brief Repeatable Battery (BRB)
Description
Participants will perform the entire Brief Repeatable Battery before and after the intervention. Using the categorization developed by Sepulcher (2013), the 5 tests of the BRB will be analyzed using four cognitive domains: attention and executive functioning, verbal memory, visual memory, and word fluency. Based on the computerized cognitive training protocol employed in the current study, investigators hypothesize changes in attention and executive functioning along with visual memory in participants in the cognitive training group, followed by participants in the MMT group compared with the wait-list control participants.
Time Frame
Baseline and 4 weeks
Title
Heart Rate Variability (HRV)
Description
HRV data will be collected during worry and rumination inductions, as participants regulate their emotions, and at rest.
Time Frame
Baseline and 4 weeks
Title
Daily Emotion Regulation Diary
Description
Participants will be asked to fill out worry and ruminations using a diary-based methodology a week before the pre-intervention behavioral session and one week after the post-intervention sessions. Changes in average self-reported worry and rumination intensity, emotion regulation strategy use, and successful emotion regulation strategy implementation will be examined as a function of the intervention.
Time Frame
Baseline and 4 weeks
Title
Improvements on a Self-Report Measure of Emotion Dysregulation
Description
Emotion Dysregulation will be assessed using the Difficulties in Emotion Regulation Scale (DERS). Changes on the total score and sub-facets of DERS will be examined as a function of the intervention.
Time Frame
Baseline and 4 weeks
Title
Improvements on a Self-Report Measure of Depression
Description
Participants will be administered Beck Depression Inventory before and after the intervention. Change on this measure will be examined to assess the impact of the interventions on symptoms of depression.
Time Frame
Baseline and 4 weeks
Title
Improvements on a Self-Report Measures of Anxiety
Description
Participants will be administered Penn State Worry Questionnaire before and after the intervention. Change on this measure will be examined to assess the impact of the interventions on symptoms of worry.
Time Frame
Baseline and 4 weeks
Title
Improvements on a Self-Report Measure of Perceived Stress
Description
Participants will be administered the Perceived Stress Scale before and after the intervention. Changes in these measures will be examined as a function of the intervention.
Time Frame
Baseline and 4 weeks
Title
Improvements on a Self-Report Measure of Quality of Life
Description
Participants will be administered the Satisfaction with Life Scale before and after the intervention. Change in scores of this measure will be examined to assess changes in quality of life as a function of the interventions.
Time Frame
Baseline and 4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
59 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 30-59 years of age Score higher than or equal to 23 on the Mini Mental Status Examination (MMSE) Corrected (near and far) visual acuity of 20/40 or better No previous experience with mindfulness or continuous meditation practice Absence of other co-morbid neurological disorders Relapse free for the last 30 days No use of corticosteroids for the last 30 days Clinically definite diagnosis of MS Ability to use a computer and connect the internet from their home Generation of at least two worries and two ruminations during the daily diary portion of the study for the pre-assessment session Exclusion Criteria: Below 30 years of age or above 59 years of age Score lower than 23 on the MMSE Corrected (near or far) visual acuity of 20/40 or greater Previous experience or participation in a mindfulness program Presence of co-morbid neurological disorders such as: Alzheimers Parkinson's disease Dementia Presence of a relapse within the last 30 days Use of corticosteroids within the last 30 days Clinically isolated syndrome suggestive of MS No ability to use a computer and/or a lack of internet connection from their home No self-generated worries and ruminations in the week-long daily diary portion of the study at pre-assessment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ruchika S Prakash, PhD
Organizational Affiliation
Ohio State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Psychology, The Ohio State University
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35901401
Citation
Duraney EJ, Fisher ME, Manglani HR, Andridge RR, Nicholas JA, Prakash RS. Impact of mindfulness training on emotion regulation in multiple sclerosis: Secondary analysis of a pilot randomized controlled trial. Rehabil Psychol. 2022 Nov;67(4):449-460. doi: 10.1037/rep0000456. Epub 2022 Jul 28.
Results Reference
derived
PubMed Identifier
32378922
Citation
Schirda B, Duraney E, Lee HK, Manglani HR, Andridge RR, Plate A, Nicholas JA, Prakash RS. Mindfulness training for emotion dysregulation in multiple sclerosis: A pilot randomized controlled trial. Rehabil Psychol. 2020 Aug;65(3):206-218. doi: 10.1037/rep0000324. Epub 2020 May 7.
Results Reference
derived
PubMed Identifier
32352832
Citation
Manglani HR, Samimy S, Schirda B, Nicholas JA, Prakash RS. Effects of 4-week mindfulness training versus adaptive cognitive training on processing speed and working memory in multiple sclerosis. Neuropsychology. 2020 Jul;34(5):591-604. doi: 10.1037/neu0000633. Epub 2020 Apr 30.
Results Reference
derived

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Cognitive and Emotion Regulation Training in MS

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