Unisanté Data repository
An Online Microdata Catalog
Search in 63 datasets
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22.04.2026
Familial hypercholesterolemia is a common genetic disorder associated with premature cardiovascular disease. Genetic cascade screening is recommended but remains underused due to privacy laws that prevent clinicians from directly contacting at-risk relatives.
This open-label, multicenter, implementation randomized clinical trial (CATCH) was conducted between November 1, 2020, and October 31, 2023, at 7 cardiovascular prevention or lipid clinics across Switzerland.
In this randomized clinical trial of patient-mediated genetic cascade screening supported by a web-based platform, participation in genetic testing and detection of familial hypercholesterolemia was increased compared with usual care. These results suggest that the use of digital communication tools enhanced the reach and effectiveness of genetic screening programs within privacy-regulated health systems.
This open-label, multicenter, implementation randomized clinical trial (CATCH) was conducted between November 1, 2020, and October 31, 2023, at 7 cardiovascular prevention or lipid clinics across Switzerland.
In this randomized clinical trial of patient-mediated genetic cascade screening supported by a web-based platform, participation in genetic testing and detection of familial hypercholesterolemia was increased compared with usual care. These results suggest that the use of digital communication tools enhanced the reach and effectiveness of genetic screening programs within privacy-regulated health systems.
09.09.2026
This cross-sectional study aimed to examine the experiences of trans and nonbinary (TNB) individuals regarding the documentation and communication of sex and gender identity in healthcare settings in Switzerland. Data were collected through an online survey assessing structural factors (documentation accuracy, form inclusivity, ease of change, provider knowledge), interpersonal factors (respectful communication, perceived rejection, breach of confidentiality, medical harm), individual factors (disclosure safety, disclosure of gender identity, negative expectations, non-disclosure behavior), and healthcare avoidance. Recruitment was conducted through professional medical organizations (n = 11), LGBTIQ+ community organizations (n = 22), a targeted Instagram campaign led by Unisanté and Transgender Network Switzerland (TGNS), and snowball sampling. Data collection took place from July 10 to September 4, 2025. The dataset includes responses from 156 participants.
11.08.2026
This project aims to develop, validate, and disseminate a Job-Exposure Matrix (JEM) for night work exposure (NW‑JEM) to support epidemiological research and occupational health surveillance. The JEM provides standardized, reproducible estimates of the index of exposure to night work across occupational groups in Switzerland.
30.07.2026
This scoping review aims to gather and analyze existing digital Patient Decision Aids (PtDAs) for cancer prevention targeting socially disadvantaged women.
How to request data
Datasets are available under various modalities.
- Anonymous data are available in Open Access under a Creative Common licence.
- Coded, pseudonymized and deidentified data are available under restricted access. Most of them are regulated by the Human Research Act (HRA), therefore an approval of your project must be submitted to your cantonal ethics committee before requesting the data (HRO, chap. 3). Details are available on the study webpage.
To get access to data, the following procedure must be followed:
Important: Before submitting a request, please check whether the data is at all useful for your project. The codebooks with the corresponding information are filed under Documentation and do not require registration.