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Neuropsychological Profile of a Patient's Group With Multiple Sclerosis and Effect of a Cognitive Rehabilitation Program (MS_Rehab)

Primary Purpose

Cognitive Dysfunction

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cognitive training
Placebo task
Sponsored by
Aveiro University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cognitive Dysfunction focused on measuring Cognitive training, Multiple sclerosis, Cognitive deficits

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with MS diagnosed according to McDonald criteria from 2010 and clinical isolated syndrome patients.
  • Age ≥18 years old.
  • Informed consent.

Exclusion Criteria:

  • Disease relapse in the last month.
  • Corticotherapy in the last month.
  • Expended Disability Status Scale score >6,0.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Intervention group

    Placebo group

    Arm Description

    Cognitive training.

    Placebo task.

    Outcomes

    Primary Outcome Measures

    Effect of an intensive cognitive rehabilitation program in neuropsychological performance of a population of patients with multiple sclerosis or clinical isolated syndrome.
    Two neuropsychological assessments were made: at baseline and at 3 months with the same neuropsychological battery to all the patients. After that, the statistically significant differences between the two study groups (comparing the standard deviations from the normative values of each test), will be accessed. The tests will be analysed separately and globally as a battery.

    Secondary Outcome Measures

    Neuropsychological profile of a population of patients with multiple sclerosis or clinical isolated syndrome.
    Characterization of the cognitive profile of deficits in the following domains (percentage of deficits by domain, considering all patients who have done the baseline evaluation): global efficiency, processing speed, attention, memory and executive functions.
    Percentage of patients with Cognitive Dysfunction
    Patients with performance >1standard deviation below the median in ≥3 tests of the battery of neuropsychological evaluation will be considered as having Cognitive Dysfunction.
    Relation between Expended Disability Status Scale score and cognitive dysfunction.
    Patients with performance >1standard deviation below the median in ≥3 tests of the battery of neuropsychological evaluation will be considered as having Cognitive Dysfunction. Correlation between Expended Disability Status Scale score and Cognitive Dysfunction.
    Impact of depression on neuropsychological performance.
    Patients with performance >1standard deviation below the median in ≥3 tests of the battery of neuropsychological evaluation will be considered as having Cognitive Dysfunction. Correlation between Hospital Anxiety and Depression Scale score and Cognitive Dysfunction.
    Relation between cognitive dysfunction and the 9-hole peg test.
    Patients with performance >1standard deviation below the median in ≥3 tests of the battery of neuropsychological evaluation will be considered as having Cognitive Dysfunction. Correlation between 9-hole peg test time frame (in seconds) and Cognitive Dysfunction.
    Relation between cognitive dysfunction and the 25-foot walk test.
    Patients with performance >1standard deviation below the median in ≥3 tests of the battery of neuropsychological evaluation will be considered as having Cognitive Dysfunction. Correlation between 25-foot walk test time frame (in seconds) and Cognitive Dysfunction.

    Full Information

    First Posted
    September 18, 2013
    Last Updated
    July 16, 2014
    Sponsor
    Aveiro University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02193906
    Brief Title
    Neuropsychological Profile of a Patient's Group With Multiple Sclerosis and Effect of a Cognitive Rehabilitation Program
    Acronym
    MS_Rehab
    Official Title
    Neuropsychological Profile of a Portuguese Patient's Group With Multiple Sclerosis and Results of a Cognitive Rehabilitation Program
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2014
    Overall Recruitment Status
    Unknown status
    Study Start Date
    December 2012 (undefined)
    Primary Completion Date
    June 2013 (Actual)
    Study Completion Date
    December 2014 (Anticipated)

    3. Sponsor/Collaborators

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

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of the study is to determine the effect of an web-based intensive cognitive rehabilitation program in neuropsychological performance of a population of patients with multiple sclerosis or clinical isolated syndrome.
    Detailed Description
    Objectives Primary: 1. To determine the effect of an intensive cognitive rehabilitation program in neuropsychological performance of a population of patients with multiple sclerosis or clinical isolated syndrome. Secondary: To characterize the neuropsychological profile of a population of patients with multiple sclerosis or clinical isolated syndrome. To evaluate the relation between Expended Disability Status Scale score and cognitive dysfunction. To evaluate the impact of depression on neuropsychological performance. To evaluate the relation between cognitive dysfunction and the 9-hole peg test. To evaluate the relation between cognitive dysfunction and the 25-foot walk test. Population and Sample Patients will be selected from an electronic database that exists in Centro Hospitalar Entre Douro e Vouga. They will be consecutively convoked and it will be proposed neuropsychological evaluation and participation in the study. Every patient will have a baseline neuropsychological evaluation (table 1). After that, they will be randomized for training (Cogweb® program or Cogweb Monthly Notebooks®) or placebo in a 2(training):1(placebo) fashion (online program of randomization). After a 3-month period of tasks (training versus placebo), they will have another neuropsychological evaluation with the same battery used for baseline. Patients included in intervention arm that have computer with internet access at home will perform a minimum of 3 sessions per week of Cogweb® during 3 months. Patients included in intervention arm that don't have computer with internet access at home will perform a minimum of 3 sessions per week of Cogweb Monthly Notebooks® during 3 months. Patients included in placebo arm will have to complete a task (send an email with a copy of a journal/magazine heading) a minimum of 3 times a week. Every patient included will have an outpatient appointment in the end of the first and second months of tasks (training versus placebo). The placebo group is a group of patients with multiple sclerosis, selected according to inclusion and exclusion criteria, from the same database than those assigned for training. The neuropsychological evaluation plan comprises: global efficiency (Montreal Cognitive Assessment test); processing speed (reading task of Stroop test, symbol searching from Wechsler Adult Intelligence Scale); attention (letter cut of Behavioural Inattention Test, Trail making test part B); memory (Letter and number sequence of Wechsler Memory Scale, digit memory, spatial localization of Wechsler Memory Scale, logic memory of Wechsler Memory Scale, word list from Wechsler Memory Scale); executive functions (colour naming task of Stroop test, inhibition from INECO frontal screening, verbal initiative from Lisbon Dementia Evaluating Battery, Zoo Map from Ineco, Matrix from Wechsler Adult Intelligence Scale) and anxious and depressive symptoms (Hospital Anxiety and Depression Scale). Sample Size There will be convoked 75 patients (convenience sample). Design Experimental, single-center study. Clinical Practice Concomitant medication allowed Any except corticotherapy. Discontinuation criteria Desire of the patient to end participation in the study. Noncompliance of the intervention plan or fail the appointments predetermined. Parameters to evaluate de study objectives Neuropsychological battery: performed at baseline and at 3 months after the completion of study tasks (each test is composed of numerical, continuous variables). Expended Disability Status Scale score: screening at baseline. Stage of the disease: screening from the database. Number of years of disease evolution. 9-hole peg test: performed at baseline and at 3 months after the completion of study tasks. 25-foot walk test: performed at baseline and at 3 months after the completion of study tasks. Efficacy Endpoints Primary: To determine if an intensive cognitive rehabilitation program changes, in a statistically significant way, the performance on a neuropsychological evaluation after 3 months of training, comparing to the control group (number of tests scored more than one standard deviation from the normal value). There will be analyzed the total and partial scores for each test. The individuals with cognitive deficits at baseline will be analyzes as rehabilitation group. The others (without cognitive deficits in cognitive evaluation at baseline) will be analyzed as a separated group of cognitive stimulation. Secondary: To characterize the profile of a population of patients with multiple sclerosis, according to the performance in a neuropsychological battery, in terms of processing speed, attention, memory and executive functions. To determine the percentage of patients with Cognitive Dysfunction, defined as performance >1standard deviation below the median in ≥3 tests of the battery. To correlate the Expended Disability Status Scale score with the Cognitive Dysfunction. To correlate the Hospital Anxiety and Depression Scale score with the Cognitive Dysfunction. To correlate the 9-hole peg test with the Cognitive Dysfunction. To correlate the 25-foot walk test with the Cognitive Dysfunction. Safety Endpoints Not applicable.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cognitive Dysfunction
    Keywords
    Cognitive training, Multiple sclerosis, Cognitive deficits

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    75 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention group
    Arm Type
    Experimental
    Arm Description
    Cognitive training.
    Arm Title
    Placebo group
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo task.
    Intervention Type
    Other
    Intervention Name(s)
    Cognitive training
    Intervention Description
    Every patient will have 3 neuropsychological evaluations (with the same battery): baseline, after a 3-month period of training and 6 months after the conclusion of the training. Patients who have computer with internet access at home will perform a minimum of 3 sessions per week of Cogweb® during 3 months. Patients who don't have computer with internet access at home will perform a minimum of 3 sessions per week of Cogweb Monthly Notebooks® during 3 months. Every patient included will have an outpatient appointment in the end of the first and second months of training.
    Intervention Type
    Other
    Intervention Name(s)
    Placebo task
    Intervention Description
    Every patient will have 3 neuropsychological evaluations (with the same battery): baseline, after a 3-month period of training and 6 months after the conclusion of the training. Patients will have to complete a placebo task (send an email with a copy of a journal/magazine heading) a minimum of 3 times a week, for 3 months. Every patient included will have an outpatient appointment in the end of the first and second months of training.
    Primary Outcome Measure Information:
    Title
    Effect of an intensive cognitive rehabilitation program in neuropsychological performance of a population of patients with multiple sclerosis or clinical isolated syndrome.
    Description
    Two neuropsychological assessments were made: at baseline and at 3 months with the same neuropsychological battery to all the patients. After that, the statistically significant differences between the two study groups (comparing the standard deviations from the normative values of each test), will be accessed. The tests will be analysed separately and globally as a battery.
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    Neuropsychological profile of a population of patients with multiple sclerosis or clinical isolated syndrome.
    Description
    Characterization of the cognitive profile of deficits in the following domains (percentage of deficits by domain, considering all patients who have done the baseline evaluation): global efficiency, processing speed, attention, memory and executive functions.
    Time Frame
    Baseline
    Title
    Percentage of patients with Cognitive Dysfunction
    Description
    Patients with performance >1standard deviation below the median in ≥3 tests of the battery of neuropsychological evaluation will be considered as having Cognitive Dysfunction.
    Time Frame
    Baseline
    Title
    Relation between Expended Disability Status Scale score and cognitive dysfunction.
    Description
    Patients with performance >1standard deviation below the median in ≥3 tests of the battery of neuropsychological evaluation will be considered as having Cognitive Dysfunction. Correlation between Expended Disability Status Scale score and Cognitive Dysfunction.
    Time Frame
    Baseline
    Title
    Impact of depression on neuropsychological performance.
    Description
    Patients with performance >1standard deviation below the median in ≥3 tests of the battery of neuropsychological evaluation will be considered as having Cognitive Dysfunction. Correlation between Hospital Anxiety and Depression Scale score and Cognitive Dysfunction.
    Time Frame
    Baseline
    Title
    Relation between cognitive dysfunction and the 9-hole peg test.
    Description
    Patients with performance >1standard deviation below the median in ≥3 tests of the battery of neuropsychological evaluation will be considered as having Cognitive Dysfunction. Correlation between 9-hole peg test time frame (in seconds) and Cognitive Dysfunction.
    Time Frame
    Baseline
    Title
    Relation between cognitive dysfunction and the 25-foot walk test.
    Description
    Patients with performance >1standard deviation below the median in ≥3 tests of the battery of neuropsychological evaluation will be considered as having Cognitive Dysfunction. Correlation between 25-foot walk test time frame (in seconds) and Cognitive Dysfunction.
    Time Frame
    Baseline
    Other Pre-specified Outcome Measures:
    Title
    Long term effects of an intensive cognitive rehabilitation program in neuropsychological performance of a population of patients with Expended Disability Status Scale.
    Description
    Two neuropsychological assessments were made: at baseline and at 9 months with the same neuropsychological battery to all the patients included who performed the 3months cognitive training or placebo tasks. After that, the statistically significant differences between the two study groups (comparing the standard deviations from the normative values of each test), will be accessed. The tests will be analysed separately and globally as a battery.
    Time Frame
    9 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients with MS diagnosed according to McDonald criteria from 2010 and clinical isolated syndrome patients. Age ≥18 years old. Informed consent. Exclusion Criteria: Disease relapse in the last month. Corticotherapy in the last month. Expended Disability Status Scale score >6,0.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Vitor T Cruz, MD
    Organizational Affiliation
    Clinical Research Office - Health Sciences Department
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Ivânia A Alves, MD
    Organizational Affiliation
    Clinical Research Office, Health Sciences Department
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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