Feasibility study: Evaluation of methods for continuous pain assessment based on contactless recording of vital and activity parameters

Feasibility study: Evaluation of methods for continuous pain assessment based on contactless recording of vital and activity parameters - Optic Pain Score

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00013579

Enrollment

Registered

2017-12-12

Start date

2017-12-19

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I48.1 R52.0

Interventions

Group 1: Patients undergoing selected routine EP-studies with only mild or no sedation are evaluated. Vital Signs (heart frequency, blood pressure, oxygen saturation) and pain level mentioned by the p

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients undergoing selected routine EP-studies with only mild or no sedation are evaluated.

Exclusion criteria

Exclusion criteria: patients not fullfilling the above mentioned criteria as well as patients with cognitive impairments and severe presbyakusis.

Design outcomes

Primary

Measure	Time frame
Patterns of Mimics and vital Parameters derived with the help of the camera. Data are analysed and evaluated to what extent they can be used to assess pain Levels and develop a reliable pain score.	—

Countries

Germany

Contacts

Public ContactKerstin Bode

Herzzentrum Leipzig GmbH Klinik für Innere Medizin/Kardiologie Abteilung für Rhythmologie

kerstin.bode@helios-gesundheit.de0341 865 251094

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026