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

Recruiting

• Conditions: I48.1; R52.0; Persistent atrial fibrillation; Acute pain

• Registration Number: DRKS00013579
• Lead Sponsor: Herzzentrum Leipzig GmbH Klinik für Innere Medizin/Kardiologie Abteilung für Rhythmologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-12-12
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

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

Exclusion Criteria

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

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.