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Next SwiSCI survey has been started!

The next community survey of SwiSCI pathway 2 will be started in the beginning of March 2017, 5 years after the first survey in 2012. About 4500 persons will receive an invitation to participate in the comprehensive survey, covering all areas of the lived experience that persons with spinal cord injury in Switzerland have.

The community survey is the first study aiming to include all persons aged 16 years or more, living with traumatic or non-traumatic SCI in Switzerland. The overall goal is to describe the SCI community in Switzerland in the long-term and to collect prevalence data on functioning and disability.

Compared to 2012, the structure of the questionnaire has been changed. Instead of three questionnaires, each participant will be requested to complete two questionnaires. These two modules are designed to ensure the longitudinal follow-up assessment of SwiSCI community survey 2012 and at the same time cover all items of the International SCI questionnaire (InSCI)

  

Wheelchair driver

Cohort Study

Swiss Spinal Cord Injury Cohort Study - SwiSCI - is a comprehensive cohort study for persons with spinal cord injuries (SCI) in Switzerland, funded by Swiss Paraplegic Foundation.

The core research of SwiSCI focuses on many aspects of functioning, health and quality of life of persons with SCI along the continuum of care, in the community and along their life span.

SwiSCI intends to establish a scientific basis for cost-effective and evidence-based care for people with SCI in the clinical and community setting. Furthermore the study will help to optimize procedures and planning of specialized services in Switzerland and elsewhere. SwiSCI has role model character for multi-disciplinary rehabilitation research in Switzerland.

Study Aims

In order to better understand and optimize the quality of life and health of persons with SCI SwiSCI strives for three special aims:

  1. the development of comprehensive knowledge on functioning, disability, health and aging with SCI in Switzerland;
  2. the identification of approaches centering in optimizing care, for example the use of devices, or decisions by law influencing the SCI population;
  3. the development of an epidemiologic database containing broad information on the characteristics of spinal cord injuries for health professionals, researchers and stakeholders in social and health care policy;
  4. provide a research platform for nested and joint projects and develop research capacity.

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