Timely identification of cognitive decline in multiple sclerosis (part of the Don*t be late! study)
Recruiting
- Conditions
- MSMultiple Sclerosis1000381610012303
- Registration Number
- NL-OMON54277
- Lead Sponsor
- Vrije Universiteit Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 750
Inclusion Criteria
- Confirmed MS diagnosis according to the McDonald 2017 criteria
- Age between 18 and 67
- No recent changes in disease modifying therapy (i.e., no changes in last 3
months)
- No current relapse or steroid treatment in the six weeks prior to the study
visit
Exclusion Criteria
- Patients with neurological (other than MS) and psychiatric disorders
- A current or history of drug or alcohol abuse
- Being unable to speak or read Dutch
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main outcome measures are: Sensitivity, specificity, negative and positive<br /><br>predictive value of Multiple Screener© compared to the gold standard (MACFIMS).</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary outcome measures include the test-retest reliability of the Multiple<br /><br>Screener© and the relationships between cognitive functioning (as measured with<br /><br>the Multiple Screener© and the MACFIMS test batter) and psychological,<br /><br>work-related and qualty of life measures. Additionally, the experiences with<br /><br>the discussion and assessment of cognitive functioning are secondary outcome<br /><br>measures. </p><br>