CompletedRelapsing MSNCT02486640

What it found

Result in a paper, not read yet

A paper reports the results; we have not read it yet. See Papers below.

What was tested

Treatment tested

What it measured

Main measures

  • Compliance to therapy (%)

    12 months

  • Persistence of therapy (Yes or No)

    12 months

  • Overall adherence to therapy (Yes or No)

    12 months

    Quality of life (reported by participants)

Other measures (5)

  • Satisfaction with the BETACONNECT autoinjector, recorded by the patient questionnaire

    Up to 24 months

    Quality of life (reported by participants)
  • Adherence to Betaferon treatment is associated with: depression, health related quality of life, coping mechanisms, self-management mechanisms, social support, fatigue, and cognition. (Yes or No)

    Up to 24 months

    Thinking and memoryFatigueMood and sleepQuality of life (reported by participants)
  • Adherence to Betaferon treatment is associated with number of relapses (Yes or No)

    12 months, 24 months

    RelapsesQuality of life (reported by participants)
  • Adherence to Betaferon treatment is associated with EDSS change (Yes or No)

    12 months, 24 months

    Disability progressionQuality of life (reported by participants)
  • Adherence to Betaferon treatment is associated with utilities of treatment, recorded by the EQ-5D quality of life questionnaire (Yes or No)

    Up to 24 months

    Quality of life (reported by participants)

Who could take part

Relapsing MS · 18 and over

Inclusion Criteria: * Patients aged ≥ 18 years with the diagnosis of relapsing remitting multiple sclerosis or a clinically isolated syndrome * Patients on treatment with Betaferon or the decision to treat patients with Betaferon has been made by the attending physician * Patients using or willing to use the BETACONNECT autoinjector for Betaferon application * Written informed consent Exclusion Criteria: * Patients receiving any other disease modifying drug * Contraindications of Betaferon described in the Summary of Product Characteristics * Patients participating in any other clinical or non-interventional study, evaluating MS therapy

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

This study aims to evaluate potential predictors of adherence by investigating a representative cohort of MS patients in Germany treated with Betaferon

Papers

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Related trials

History

    1. Started

      Sept 2015

    2. Main results due

      Oct 2019

    3. Finished

      Jan 2020

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