Patiënten met problemen met bewegend functioneren Physical activity
Conditions
Interventions
None listed
Sponsors
Medisch Universitair Ziekenhuis Maastricht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: - Receiving physiotherapy treatment during hospitalisation at the MUMC+ - 18 years or older - Able to walk - Willing to participate - Sufficient understanding of the Dutch language - Able to provide written informed consent.
Exclusion criteria
Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: - Admitted to the Intensive Care or Medium Care units. - A contraindication concerning walking (as reported by the attending medical specialists in the medical record). - A contraindication to wearing the FastFocus* Vital Signs Monitoring System activity monitor at the ear (i.e.: patients with signs of skin damage on the ear, patients with pierced ears at the sensor application/measurement site, patients with skin conditions that could result in permanent harm when using the EarSensor, patients with limited blood perfusion through the ear due to medical conditions (e.g., cauliflower ears, ischemic ear shells, etc.), patients that are obliged to wear other medical devices for health and/or disability purposes (e.g., hearing aids, oxygen tubes, etc.), and/or patients in which the inner aspect of the ear (cavum conchae) is not large enough to accommodate the hook of the sensor without touching the tragus and/or crus of helix.) - Impaired cognition (dementia / delirium) as reported by the attending medical specialist in the medical record. - Incapacitated subjects as reported by the attending medical specialist in the medical record. When any doubt arises, the patient will not be considered eligible - A life expectancy shorter than 3 months as mentioned by the attending medical specialist in the medical record - Subjects that are not allowed to leave their hospital room due to isolation measures as reported in the medical record. - Pregnant or breastfeeding women. - Inability to give informed consent. - Previous participation in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome parameter: total time walking (sec.). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome parameters: total time sitting/standing (sec.), total time lying (sec.), total number of steps (n). | — |
Countries
Netherlands
Outcome results
None listed