A5035322061- Delphi Technique in Research
- Multiple Sclerosis Research Studies
- Health Policy Implementation Science
- Meta-analysis and systematic reviews
- Social Media in Health Education
- Focus Groups and Qualitative Methods
- Health Systems, Economic Evaluations, Quality of Life
- Inclusion and Disability in Education and Sport
- Family and Disability Support Research
- Impact of Technology on Adolescents
- Health and Medical Studies
- Cerebral Palsy and Movement Disorders
Carl von Ossietzky Universität Oldenburg
2021-2024
Leibniz Institute for Prevention Research and Epidemiology - BIPS
2017-2023
University of Bremen
2023
Evidence Based Research (United States)
2017
Focus groups used for data collection in health research are increasingly conducted online. In two multi-center projects, we applied available methodological instructions synchronous online focus (SOFGs). We describe necessary changes and specifications regarding the planning (recruitment, technology, ethics, appointments) conduct (group composition, moderation, interaction, didactics) to enhance knowledge about of SOFGs.Recruiting proved be challenging necessitated direct analogue...
Introduction The Cochrane Collaboration aims to produce relevant and top priority evidence that responds existing gaps. Hence, research setting (RPS) is important identify which potential gaps are deemed most important. Moreover, RPS supports future health conform both needs. However, studies prioritising systematic review topics in public surprisingly rare. Therefore, inform the agenda of Public Health Europe (CPHE), we introduce protocol a study on several European countries,...
Abstract Background Research priority setting (RPS) studies are necessary to close the significant gap between scientific evidence produced and stakeholders need. Their findings can make resource allocation in research more efficient. However, no general framework for conducting an RPS study among public health exists. rare such has been previously conducted published Germany. Therefore, we aimed investigate which topics prioritised by relevant Methods Our consisted of a scoping stage Delphi...
Background Previous investigations of multiple sclerosis (MS)-related healthcare have focused on utilisation specific individual health services (e.g. hospital care, office-based neurologists) by people with MS (PwMS). Meanwhile, little is known about possible patterns across and their potential differences patient characteristics. Objective To comprehensively analyse identify MS-related service detect characteristics explaining such patterns. Methods In 2021, we invited all PwMS insured the...
Objectives This study aimed to develop and apply a structured approach for prioritising topics systematic reviews in public health, framed according the readily applicable PICO format, which encourages involvement of stakeholders’ preferences transparent matter. Methods We developed multi-stage process, consisting scoping two Delphi stages with web-based surveys invited health stakeholders Switzerland participate: First, respondents specified different domains, were reformulated format by...
ABSTRACT Introduction People with multiple sclerosis and gait impairment are particularly susceptible to facing restrictions in their participation. This study aims investigate (a) which contextual factors within the framework of International Classification Functioning, Disability Health (ICF) relevant for participation from perspective people who (intend to) use mobility assistive devices, (b) how these shape subjective facets participation, including a sense connection, efficacy meaning,...
Background Multiple sclerosis (MS) is the most common autoimmune inflammatory disease of central nervous system in Europe, often causing severe physical, cognitive and emotional impairments. Currently, it unclear whether healthcare provisions people with MS (PwMS) are line recommendations for treatment based on guidelines or patients’ needs. The main objectives study as follows: (a) to investigate how well PwMS treated; (b) develop a needs-oriented, patient-centred care model. Methods This...
Einleitung In Deutschland leben etwa 220.000 Menschen mit Multipler Sklerose (MS). Das vom Innovationsfonds geförderte Projekt untersucht die Versorgungssituation von MS-Erkrankten in Niedersachsen, um Handlungsempfehlungen für eine Verbesserung der Versorgung abzuleiten. Es werden Charakteristika MS-Erkrankten, sich an einer Online-Befragung beteiligt haben, denen Grundgesamtheit verglichen.