NCT06336252Completed
Technology Assisted Nudging to Increase Physical Activity Among Hospitalised Medical Patients
Technology Assisted Nudging to Increase Physical Activity Among Hospitalised Medical Patients in Hospital and 3 Months After Discharge
Source: ClinicalTrials.gov · Last updated 7 Jul 2026
Brief summary (registry, in English)
Primary Objective To investigate if patients hospitalised for older adults with a decreased level of physical function, either related to a chronic condition e.g., COPD, Congestive heart failure, renal failure; infections; frailty and tendency of falling; orthopaedic surgery - after hip fracture will increase their time spent out of bed during hospitalisation and 3 months after discharge through visual feedback and motivational intervention about physical activities from a new mobile technology. Hypothesis Patients hospitalised for medical disease will increase their physical activity level during hospitalisation and 3 months after discharge through visual feedback and motivational intervention from a new mobile technology.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 130 (actual)
- First submitted
- 13 Mar 2024
- Start date
- 3 May 2024
- Primary completion date
- 7 Jun 2025
- Lead sponsor
- Bispebjerg Hospital
- Diseases
- Heart failure, Stroke, COPD, Parkinson disease
- NCT number
- NCT06336252
What you commit to
- Study type: Interventional
- Participants enrolled: 130
- From 3 May 2024 to the primary completion date, 7 Jun 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Any condition that, in the opinion of the investigator, makes the person unfit for participation, e.g., delirium and/or psychotic symptoms; moderate or severe depression (GDS\>8 (short form)); major surgery; moderate/severe dementia (MoCA≤18); chemotherapy or radiation treatment ongoing at enrolment; moderate/severe frailty (CFS≥6)
- Has allergy towards band aid
Other
- An individual will be excluded from the study if he/she meets any of the following criteria:
- Expected hospitalisation less than 24 hours
- Enrolled in any other clinical study within the duration of the current study.
- While these criteria represent the criteria for being observed, only patients observed for at least 24 hours are included in the analysis population. For practical reasons it is not possible to predict those patients eligible for the analysis population at inclusion. Hence, we will monitor more patients than we will analyse (see statistical analysis section).
Who the study is looking for
- An individual will be eligible for study participation if he/she meets the following criteria:
- Aged ≥60
- Is admitted to one of the participating departments
- Has signed informed consent
- Reads and speaks Danish, Norwegian, Italian, or English
Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Christian Dall Coordinator of this site? Confirm its status | Copenhagen | Denmark | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.