Prospective observational study on wearable-based monitoring of patients in hip and knee arthroplasty

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00038083

Enrollment

400

Registered

2025-10-13

Start date

2026-01-05

Completion date

Unknown

Last updated

2025-11-24

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

Conditions

Total hip and knee replacement

Interventions

Group 1: In patients undergoing elective knee or hip arthroplasty, vital parameters are measured perioperatively until discharge using a wearable device, with real-time data transmission to the nursin

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: elective total hip or knee replacement

Exclusion criteria

Exclusion criteria: missing consent

Design outcomes

Primary

Measure	Time frame
Acceptance and compliance of nursing staff and patients regarding wearable-based monitoring (workload, satisfaction, wearing comfort, digital barriers). This is assessed for patients using a questionnaire completed daily and at discharge, and for nursing staff using a questionnaire administered every three months.	—

Secondary

Measure	Time frame
Continuous recording of vital parameters until discharge (heart rate, ECG, respiratory rate, oxygen saturation, body temperature, fall detection); recording of vital parameters using conventional monitoring for 24 hours postoperatively; patient characteristics; perioperative complications (surgical and non-surgical).	—

Countries

Germany

Contacts

Public ContactAnne Postler

Universitätscentrum für Orthopädie, Unfall- und Plastische Chirurgie, Universitätsklinikum Carl Gustav Carus Dresden

anne.postler@ukdd.de+493514580

Outcome results

None listed

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