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Observational Study to Analyse the Impact of Nurse Support and Disease Related Factors on Long- Term Adherence to Betaferon Treatment

Betaferon Prospective Study on Adherence, Coping and Nursing Support

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00787657
Acronym
BEACON
Enrollment
1723
Registered
2008-11-07
Start date
2008-06-30
Completion date
2014-10-31
Last updated
2015-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsing Remitting Multiple Sclerosis (RRMS)

Keywords

Clinically Isolated Syndrome (CIS)

Brief summary

* The Study analyses the influence of selected factors on adherence to Betaferon treatment in patients with early multiple sclerosis (MS). The Investigator will document the relevant medical data regarding multiple sclerosis at every hospital visit, the patient will fill in two questionnaires at every visit: one about coping with the disease and the other about anxiety and depression. * The Study particularly looks at the role of the support of the patient given by the multiple sclerosis nurses.The nurse will provide additional standardised information at start of treatment and will regularly phone the patient to ask standardised questions about the general condition with regard to the treatment, the disease and social support. At the end of the Study it will be assessed if the supportive measures and the standards in terms of adherence management in the hospital have some influence to increase long-term treatment adherence.

Interventions

Patients after first clinical events suggestive of MS (according to SMPC) and patients with RRMS within the first two years of diagnosis

Sponsors

Bayer
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients after first clinical event suggestive of multiple Sclerosis (MS) (according to SmPC) and patients with Relapsing / Remitting Multiple Sclerosis (RRMS) within the first two years of diagnosis.

Exclusion criteria

* Contra-indications as indicated in Betaferon summary of Products Characteristics (SmPC)

Design outcomes

Primary

MeasureTime frame
Proportion of patients adhering to treatment6, 12, 18 and 24 months

Secondary

MeasureTime frame
Rate of early treatment termination6, 12, 18 and 24 months
Rate of study dropout6, 12, 18 and 24 months
Predictive value of BL parameters, WCQ, HADS, RODQ12 and 24 months
RODQ (Risk of Dropout Questionnaire)Monthly over 6 months; every other month thereafter
HADS (Hospital Anxiety and Depression Scale)6, 12, 18 and 24 months
EDSS (Expanded Disability Status Scale)6, 12, 18 and 24 months
Relapse rate6, 12, 18 and 24 months
WCQ (Ways of Coping Questionnaire)6, 12, 18 and 24 months

Countries

Argentina, Bahrain, Belgium, Bosnia and Herzegovina, Canada, China, Colombia, Czechia, Egypt, Estonia, France, Germany, Iran, Israel, Italy, Jordan, Kuwait, Lebanon, Libya, Mexico, Netherlands, New Zealand, Norway, Pakistan, Portugal, Saudi Arabia, Singapore, Slovakia, Slovenia, South Korea, Sweden, Syria, Taiwan, United Arab Emirates, United Kingdom, Venezuela

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026