If you are an informal caregiver (family member, partner, friend) supporting a person with Parkinson’s disease in their daily life, this is the survey for you!

You will be asked questions about yourself as well as the person you support.

• Your personal socio-demographic information, daily routines as a caregiver, perspective towards using technology for health reasons (e.g. computer, smartphone, mobile applications).
 
• Information about the person you support – healthcare professionals and types of help he/she receives, year of diagnosis etc.

After completing the survey, you will be able to indicate if you want to participate in the next steps of the study such as face-to-face interviews (ca. 1 hour) and/or group workshops (ca. 2 hours including a break).