Trial Condition(s):

Relapsing Remitting MS (RRMS), Secondary Progressive MS (SPMS)

BetaPlus Survey – Observational study to assess drug adherence in patients with multiple sclerosis after conversion to Betaferon® by using elements of the BetaPlus Program

Bayer Identifier:

14192

ClinicalTrials.gov Identifier:

NCT01233245

EudraCT Number:

Not Available

Study Completed

Trial Purpose

This is an observational survey to assess the factors that influence adherence to Betaferon therapy in multiple sclerosis patients using elements of the BetaPlus support program, including the nurse support and auto-injectors. The patients were evaluated under normal clinical practice and were asked to fill out the quality of life FAMS questionnaire, Coping processes (WCQ - Ways of Coping Questionnaire) and depression questionnaire CES-D.

Inclusion Criteria
- Relapsing-remitting MS (RRMS) or secondary-progressive MS (SPMS)
 - Previous treatment with disease modifying drugs
 - Adjustment of disease modifying treatment necessary at the discretion of the investigator
 - Switch to Betaferon at least 1 month but not longer than 3 months prior to inclusion
Exclusion Criteria
- Patients not fulfilling the indications in the local prescribing information
 - Refusal to sign inform consent

Trial Summary

Enrollment Goal
1077
Trial Dates
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Phase
N/A
Could I receive a placebo?
No
Products
Betaseron (Interferon beta-1b, BAY86-5046)
Accepts Healthy Volunteers
No

Where to Participate

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Locations
Status
LocationsStatus
Locations

Investigative Site

Many Locations, Germany

Status
Completed
 
Locations

Investigative Site

Many Locations, France

Status
Completed
 
Locations

Investigative Site

Many Locations, Italy

Status
Completed
 
Locations

Investigative Site

Many Locations, Spain

Status
Completed
 
Locations

Investigative Site

Many Locations, Netherlands

Status
Completed
 
Locations

Investigative Site

Many Locations, Czech Republic

Status
Completed
 
Locations

Investigative Site

Many Locations, Israel

Status
Completed
 
Locations

Investigative Site

Many Locations, Portugal

Status
Completed
 
Locations

Investigative Site

Many Locations, Turkey

Status
Completed
 
Locations

Investigative Site

Many Locations, South Korea

Status
Completed
 
Locations

Investigative Site

Many Locations, Taiwan, China

Status
Completed
 
Locations

Investigative Site

Many Locations, Saudi Arabia

Status
Completed
 
Locations

Investigative Site

Many Locations, Iran

Status
Completed
 
Locations

Investigative Site

Many Locations, Jordan

Status
Completed
 
Locations

Investigative Site

Many Locations, Lebanon

Status
Completed
 

Trial Design