R52.0 R52.2
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Demand for a consultation by a pain specialist Demand of a perioperative care for the acute pain service Informed consent Patients = 18 years remaining in-patient stay = 48 h patients who are legally capable and do have the mental capacity to understand the instructions of the study personnel
Exclusion criteria
Exclusion criteria: Cancer or palliative patients Pregnants No capacity to consent Refusal to take part in the study language or communication difficulties inmates of prison or other institutions persons who are tied to the sponsor or investigator in a relationship of dependency
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Technical feasibility of a telemedical consultation with patients suffering from acute and chronic pain with the RP (remote presence)-Lite system in a clinical setting | — |
Secondary
| Measure | Time frame |
|---|---|
| Non-inferiority of the telemedical consultations using a RP-Lite system in a clinical setting, Patient and healthcare provider satisfaction / acceptance, Demographic data, Medical history, technical performance All groups will be surveyed after consultation by a standardized, validated paper-based questionnaire. | — |
Countries
Germany
Contacts
Klinik für AnästhesiologieUK Aachen