Corrona Multiple Sclerosis Registry
The objectives of the Corrona Multiple Sclerosis Registry are to create a national cohort of patients with multiple sclerosis and study the comparative effectiveness and safety of approved treatments for multiple sclerosis. Secondary objectives include analyzing the epidemiology and natural history of the disease, its comorbidities, and current treatment practices.
Overview
- Acronym
- CMSR
- Website
- CMSR
- Investigators
-
- Contacts
-
General Design
- Study design
- Registry
- Start - End Year
- 2017 -
- General Information on Follow Up (profile, frequency)
-
Longitudinal follow-up data is collected from both patients and their treating neurologist every 6 months during routine clinical encounters.
- Recruitment Target
-
- Individuals
- Number of Participants
- 1,000
- Supplementary Information
-
The design is a prospective, observational registry for patients with multiple sclerosis under the care of a board certified neurologist.
Access
Availability of data and biosamples
| Possible Access to Data | |
| Possible Access to Biosamples | |
| Other |
|
Supplementary Information
https://clinicaltrials.gov/ct2/show/study/NCT03291756.
Timeline
Population
CMSR population
The population consists of American patients with multiple sclerosis who are 18 years of age or older.
Selection Criteria
- Minimum age
-
18
- Countries
-
- United States of America
- Health Status
-
- Diagnosis of multiple sclerosis
- Other Criteria
-
Willing and able to provide Personally Identifiable Information (PII) which includes the following types of personal information at a minimum: full name, date of birth, sex, and home address zip code.
Exclusion: participating in or planning to participate in a clinical trial with a non-marketed or marketed investigational drug (i.e. phase I-IV drug trial).
Sources of Recruitment
- Specific Population
-
- Clinic patients
- Supplementary Information
-
Patients volunteer to be enrolled in the Multiple Sclerosis Registry during regularly scheduled office visits.
Sample Size
- Number of Participants
- 1,000
Data Collection Events
| # | Name | Data sources | Data sources - Biosamples | Start | End |
|---|---|---|---|---|---|
| 0 | CMSR - Enrollment |
|
2017 (August) | Ongoing | |
| 1 | CMSR - Visit 1 |
|
2018 (February) | 2018 (July) | |
| 2 | CMSR - Visit 2 |
|
2018 (August) | 2019 (January) | |
| 3 | CMSR - Visit 3 |
|
2019 (February) | 2019 (July) | |
| 4 | CMSR - Visit 4 |
|
2019 (August) | 2020 (January) | |
| 5 | CMSR - Visit 5 |
|
2020 (February) | Ongoing |
Participating Studies
| Acronym | Name | Study design | Countries |
|---|
Harmonization Initiatives Included
| Acronym | Name |
|---|
Datasets
| Name | Data Collection Events | Variables |
|---|
Areas of Information Collected
- Socio-demographic and economic characteristics
- Death
- Lifestyle and behaviours
- Physical measures and assessments
- Birth, pregnancy and reproductive health history
- Laboratory measures
- Perception of health, quality of life, development and functional limitations
- Cognition, personality and psychological measures and assessments
- Diseases
- Life events, life plans, beliefs and values
- Symptoms and signs
- Preschool, school and work life
- Medication and supplements
- Social environment and relationships
- Non-pharmacological interventions
- Physical environment
- Health and community care services utilization
- Administrative information
Variables Content Summary
Areas of Information Collected
No Areas of Information Collected
No Scales Collected
Areas of Information Collected per per Population and Data Collection Event
No Areas of Information Collected
No Scales Collected
Networks
| Acronym | Name | Harmonization Initiatives | Individual Studies |
|---|
Last Update: 2023-08-10T18:18:22.258