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ZEG Berlin GmbH

Zentrum für Epidemiologie und Gesundheitsforschung

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About QSF

Background

Following the success of the two gender-specific HRQoL scales, the diagnostic tools research group focused on developing a single instrument that could be used across genders.  

The starting point for the development of the Quality of Sexual Function Scale (QFS) was the three domains (psychological, somato-vegetative and sexual/urogential) used in both the Menopause Rating Scale (MRS) and the Aging Males’ Symptoms Scale (AMS).  The development team also reviewed existing scales for male and female sexual dysfunction and concluded that common experiences are common also across gender. Moreover, two people are usually required to define the quality of sexual life.  

Objectives

  • Develop a self-administrable scale that is short and easy to complete 
  • Application across genders, age, ethnicity, social class and health status
  • High acceptance in men and women
  • Inclusion of the view of the partner 
  • To develop a tool that is easy to analyze and can be applied to clinical and observational research
  • To develop a tool that could also be used as an outcome measure for interventions or therapy

The concept for the development followed recommendations for Patient-Reported Outcomes (PRO) Measures as published by FDA.

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Expertise

  • Non-interventional study design
  • Post-authorization safety studies
  • Post-authorization efficacy studies
  • Cohort studies
  • Case-control studies
  • Medical Devices
  • Patient Reported Outcomes (PROs)
    • Aging Male Symptoms Scale
    • Menopause Rating Scale
    • Scale for Quality of Sexual Function
    • Short Term Hormone Effect Scale
    • Research team
  • Data collection instruments

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ZEG Berlin

Berlin Center for Epidemiology and Health Research

Invalidenstraße 115
10115 Berlin
Germany

Contact Us

Expertise

  • Real-World Evidence
  • Non-interventional study design
  • Post-authorization safety studies
  • Post-authorization efficacy studies
  • Cohort studies
  • Case-control studies
  • Medical Devices
  • Patient Reported Outcomes (PROs)
  • Data collection instruments

Services

  • Crisis Management
  • Consulting
  • Data Management and Biostatistics
  • Medical Writing
  • Study Management
  • Quality Assurance
  • Pharmacovigilance

ENCePP

We are a partner centre of the ENCePP scientific network which is coordinated by the European Medicines Agency. We are dedicated to excellence in research by adhering to the ENCePP Guide on Methodological Standards and promoting scientific independence and transparency. We register studies in the ENCePP E-Register of Studies, a publicly accessible resource for the registration of pharmacoepidemiological and pharmacovigilance studies.

General Data Protection Regulation

With a view to the introduction of the GDPR/EUDSGVO we are glad to present our newupdated privacy policy . The updated description are stored under “about us” and then “privacy policy/GDPR”. Further translation for study participants will follow contemporary.

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