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

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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.


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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Nashville, TN
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Atlanta, GA
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Bala-Cynwyd, Pennsylvania 19004
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Bala-Cynwyd, PA
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Boca Raton, FL
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Cullman, AL
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Deckerville, MI
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Fairfax, VA
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Foxboro, MA
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Franklin, TN
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Fulton, MD
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Lititz, PA
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Lubbock, TX
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Medford, OR
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Memphis, TN
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New Port Richey, FL
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Round Rock, TX
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Saint Louis, MO
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Staten Island, NY
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Stratford, NJ
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Tampa, FL
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Teaneck, NJ
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Virginia Beach, VA
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