SHIFT-Hospital in Motion (Hospital Implementation Study)
SHIFT-Hospital in Motion: Use of Activity Sensors in the Clinical Setting
1 other identifier
observational
19
1 country
1
Brief Summary
The goal of this monocentric observational study involving hospitalised patients is to assess the integration of activity sensors into routine clinical practice.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Nov 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 25, 2024
CompletedFirst Submitted
Initial submission to the registry
January 9, 2025
CompletedFirst Posted
Study publicly available on registry
January 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 11, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2025
CompletedOctober 1, 2025
September 1, 2025
4 months
January 9, 2025
September 25, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Evaluation of the time expenditure
Using a study-specific questionnaire, the additional time expenditure associated with the use of activity sensors by physiotherapy and clinical care is evaluated.
Day 1-4
Secondary Outcomes (4)
Assessment of the comfort level associated with wearing the sensors
Day 2-4
Evaluation of the handling
After 10-week period (at recruitment completion)
Assessment of the accuracy of the classification algorithm for the detection of movements parameters
Day 1-3
Optimization of activity classification algorithm
After 10-week period (at recruitment completion)
Eligibility Criteria
Patients that are hospitalised for at least 3 days on the medical ward 6.1 of the University Hospital Basel and are recruited either mondays or tuesdays.
You may qualify if:
- at least 3 days inpatient on the medical ward 6.1 (Monday to a maximum of Thursday or Tuesday to a maximum of Friday)
- at least restricted bed rest
- patient must be able to walk
- patient must be cognitively able to follow instructions (normal Observation Screening Scale (DOS) und modified Confusion Assessment Method (mCAM))
- ≥ 18 years
- signed informed consent
You may not qualify if:
- planned discharge within the next 3 days
- planned surgery during the measurement
- isolated patient
- inability or contraindications to participate in the study or to follow the study procedures, e.g. due to certain neurological disorders, speech problems, mental disorders, or cognitive impairments
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Universitiy Hospital Basel, Division of Internal Medicine
Basel, Canton of Basel-City, 4031, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Joris Kirchberger
University Hospital, Basel, Switzerland
- STUDY CHAIR
Jens Eckstein, Prof. Dr. med.
University Hospital, Basel, Switzerland
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 9, 2025
First Posted
January 20, 2025
Study Start
November 25, 2024
Primary Completion
March 11, 2025
Study Completion
June 30, 2025
Last Updated
October 1, 2025
Record last verified: 2025-09