Skip to content

Postoperative mobilisation Study: utilizing digital mobilization and wearable tracking devices to promote recovery after robotic surgery

Postoperative mobilisation Study: utilizing digital mobilization and wearable tracking devices to promote recovery after robotic surgery - MOVE

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00028502
Enrollment
340
Registered
2022-05-04
Start date
2021-10-01
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

TO BE DONE

Interventions

Group 1: Patients receive a wearable activity tracker (no cloud connection) and a tablet with digital instructions for physiotherapy for autonomous mobilisation post surgery. Group 2: Patients receive

Sponsors

Helios Universitätsklinikum Wuppertal
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) All patients planned for robotic surgeries. 2) Patients must be at least 18 years old. All patients must be in the legal position for a medical consent.

Exclusion criteria

Exclusion criteria: 1) Immobility 2) Impaired mobility due to medical or orthopedic commorbidities 3) Utilization of a cane, walker or wheelchair 4) Patient cannot tolerate wearable activity tracker 5) postoperative stay on the ICU for more than 36 hours 6) Disability with respect to the eyevision 7) mental or cognitive impairment restricting consent for the survey

Design outcomes

Primary

MeasureTime frame
Primary endpoint is the step count of a patient measured with the wearable activity tracker attached the arm. The step count is differentiated as steps per day and avery step count per patient.

Secondary

MeasureTime frame
Secondary endpoints are other parameters detected by the wearable. These include heart rate, respiratory rate, heart rate variability. Secondary endpoints include both length of stay and postoperative complications.

Countries

Germany

Contacts

Public ContactFriedrich-Carl von Rundstedt

Helios Universitätsklinikum Wuppertal

Friedrich.vonRundstedt@helios-gesundheit.de02028963407

Outcome results

None listed

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