Impact of the BETACONNECT Auto-injector on BETASERON Therapy Adherence and Patient Satisfaction
Status: | Completed |
---|---|
Conditions: | Neurology |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 9/8/2018 |
Start Date: | February 5, 2016 |
End Date: | September 13, 2017 |
The primary objective of this study is to assess adherence and persistence to BETASERON
therapy in patients who are using the BETACONNECT auto-injector device (BETACONNECT device).
The secondary objective of this study is to assess patient-reported satisfaction with the
BETACONNECT device.
therapy in patients who are using the BETACONNECT auto-injector device (BETACONNECT device).
The secondary objective of this study is to assess patient-reported satisfaction with the
BETACONNECT device.
Inclusion Criteria:
- Male and females greater than or equal to 18 years of age
- Diagnosis of RRMS according to revised McDonald Criteria (2010) or (CIS)
- Prescribed BETASERON (note: decision to treat with BETASERON must be made independent
of participation in this study)
- Confirmation of insurance coverage for BETASERON treatment
- Access to a personal computer to complete online patient satisfaction survey at Week 6
Exclusion Criteria:
- Currently enrolled in a clinical trial or other observational study for Multiple
Sclerosis treatment
- Documented substance abuse within the previous 6 months prior to study enrollment
- Any major laboratory value abnormality that the investigator believes would preclude
the patient from participating in the study
- Any medical disorder, condition or history that in the opinion of the investigator
would impair the patient's ability to participate in or complete the study
- Pregnant or nursing
We found this trial at
22
sites
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