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Validation of Two Acitivity Monitors in Three Inpatient Populations.

NCT04120740 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 36

Last updated 2019-11-21

No results posted yet for this study

Summary

The aim of this study is to investigate the validity of Sens Motion and ActivPAL acitivity monitors. Thirthy-six patients from three different patient populations will be included: 12 acute high-risk abdominal surgery patients (+18 years), 12 hip fracture patients (+65) and 12 older medical patients (+65).

Each patient will be asked to wear two sets of activity monitors while performing a predefined researcher-supervised protocol consisting of a range of positions and activities including lying down, sitting, standing and walking.

Observations measured by time in each position will be used as a golden standard for physical activity and thus compared with the data produced by the acitivity monitors.

Conditions

  • Hip Fractures
  • Abdominal Surgery
  • Medical Patients

Sponsors & Collaborators

  • SENS Innovation Aps

    collaborator UNKNOWN

  • Mette Merete Pedersen

    lead OTHER

Principal Investigators

  • Mette M Pedersen, Postdoc · Hvidovre University Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-10
Primary Completion
2019-11-18
Completion
2019-11-18

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04120740 on ClinicalTrials.gov