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US PROmyBETAapp2.0: A Study to Learn More About the Medication Usage and Patient Reported Outcomes Via the myBETAapp in Medical Care of Patients With Multiple Sclerosis Treated With BETASERON Using BETACONNECT Autoinjector

US PROmyBETAapp2.0: Ascertaining Medication Usage and Patient-reported Outcomes (PROs) Via the myBETAapp™ in Patients With Multiple Sclerosis Treated With BETASERON® Using BETACONNECT™ Autoinjector

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04356339
Enrollment
100
Registered
2020-04-22
Start date
2020-11-24
Completion date
2021-11-11
Last updated
2023-07-24

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

Conditions

Multiple Sclerosis

Keywords

MS

Brief summary

In this study researchers want to learn more about the medication usage behavior among multiple sclerosis (MS) patients treated with BETASERON using the myBETAapp. Multiple sclerosis (MS) is a disease in which the covering called myelin around the nerves of the central nervous system degenerate. MS is a lifelong disease therefore requiring continuous treatment to delay the disease progression and reduce the rate of relapse (the return of signs and symptoms of). BETASERON is an approved medicine used to reduce the relapse in patients with MS. It is injected into the tissue under the skin using BETACONNECT autoinjector, which automatically captures injection data including injection date, time, speed, and depth and uploads the data into paired myBETAapp. This allows patients to organize and track their progress and share the injection information with their physicians. The medication usage behavior to be collected in this study includes the elements to what extent * taking medication matches the presciber's recommendation (adherence, compliance), * treatment for the prescribed duration (persistence) is continued and * injections were missed. Among MS patients treated with Betaferon using the myBETAapp the study will also collect information on the health-related quality of life , treatment satisfaction and satisfaction with treatment support.

Interventions

DRUGInterferon-beta-1b (BETASERON, BAY 86-5046)

Using the BETACONNECT autoinjector and myBETAapp as prescribed by the physician

Sponsors

Bayer
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Aged ≥18 years * Treated with BETASERON using the BETACONNECT autoinjector * Registered with myBETAapp * Provided electronic informed consent

Exclusion criteria

\- There are no

Design outcomes

Primary

MeasureTime frameDescription
Compliance to therapyUp to 6 monthsCompliance is defined as the the proportion of BETASERON administrations with the correct injection interval within some window. Windows will be set for each individual patient based on prescribed injection frequency.
Persistence of therapyUp to 6 monthsPersistence to BETASERON using the BETACONNECT device will be measured as the number of days between the initial BETASERON administration and the earlier of the last BETASERON administration using the BETACONNECT device or before a minimum 60-day gap in therapy.
Adherence to therapyUp to 6 monthsAdherence to BETASERON using the BETACONNECT device is a dichotomous variable (adherent or non-adherent) defined as receiving at least 80% of the expected number of injections during 6 months of treatment (or up to the point of early termination) as captured by the BETACONNECT device.

Secondary

MeasureTime frameDescription
Change in patient-reported health-related quality of life (HRQOL)Up to 6 monthsChange in patient-reported health-related quality of life (HRQOL) will be collected via an online study-specific patient survey.
Patient satisfaction with the myBETAappUp to 6 monthsPatient satisfaction with the myBETAapp will be collected via an online study-specific patient survey.
Change in health status evaluated by EQ-5D-5L descriptive systemUp to 6 monthsEQ-5D-5L is a standardized measure of general health status. The EQ-5D-5L descriptive system consists of 5 dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression), where respondents indicate their health state on each dimension based on 5 response options (no problems, slight problems, moderate problems, severe problems, and extreme problems).
Change in EQ-Visual Analog Score (EQ-VAS)Up to 6 monthsThe EQ-Visual Analog Score (EQ-VAS) allows respondents to rate their health on a 20 cm vertical, visual analog scale with endpoints labelled 'the best health you can imagine' and 'the worst health you can imagine' and provides a single quantitative measure of health.
Change in prescription and non-prescription medication usageUp to 6 monthsPrescription and non-prescription medication usage will be collected via an online study-specific patient survey.
Number of relapsesUp to 6 months
Number of participants with treatment with corticosteroids due to relapsesUp to 6 months
Number of emergency room visits due to relapseUp to 6 months
Number of hospitalizations due to relapseUp to 6 months
Patient self-assessmentUp to 6 monthsSelf-assessment includes assessment for mood, memory, vision, urinary symptoms. The assessment will be collected via an online study-specific patient survey.
Change in dose of BETASERON prescriptionUp to 6 months
Change in frequency of BETASERON prescriptionUp to 6 months
Patient satisfaction with the BETACONNECT autoinjectorUp to 6 monthsPatient satisfaction with the BETACONNECT autoinjector will be collected via an online study-specific patient survey.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026