Patients' acceptance for digital technologies in healthcare: a discrete choice experiment
- Conditions
- StrokeI64Stroke, not specified as haemorrhage or infarction
- Registration Number
- DRKS00031543
- Lead Sponsor
- Hochschule Neubrandenburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 1259
1. stroke patients (experimental group).
Patients with a diagnosis of stroke.
Preferably experience in rehabilitative therapy (neurorehabilitation)
Residence in Germany
Able to read and understand the German language
Willing and able to provide online informed consent stating that they understand the purpose and procedures of the study and are willing to participate in the study
2. general population (control group)
Resident in Germany
Able to read and understand the German language
Willing and able to provide online informed consent stating that they understand the purpose and procedures of the study and are willing to participate in the study
For both populations:
Resident in Germany
Not able to read and understand the German language
Unwilling and unable to provide online informed consent stating that they understand the purpose and procedures of the study and are willing to participate in the study
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Our primary endpoint is to weight the criteria that impact patient acceptance when interacting with digital technologies for healthcare and as an adjunct to traditional care provided by a human professional.
- Secondary Outcome Measures
Name Time Method Secondary end points include (1) a benefit-burden assessment, (2) an overall comparison of the relative importance of attributes, and (3) identification of key attributes that influence patient adherence. Our exploratory end points include (1) assessment of heterogeneity and (2) subgroup analysis.