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
About this trial
This is an interventional treatment trial for Cognitive Dysfunction focused on measuring Cognitive training, Multiple sclerosis, Cognitive deficits
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.
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
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
Learn more about this trial
Neuropsychological Profile of a Patient's Group With Multiple Sclerosis and Effect of a Cognitive Rehabilitation Program
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