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Clinical Trials/NCT04555330
NCT04555330CompletedNot Applicable

Technology Assisted Physical Activity Among Hospitalised Medical Patients

Marius Henriksen1 site in 1 country354 target enrollmentStarted: June 11, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
354
Locations
1
Primary Endpoint
Time spent out of bed measured in minutes related to the total accelerometer wear time (minutes).

Study Overview

Brief Summary

Research show that inactivity during hospitalization is the norm and that the negative effects on muscle mass and the fitness of the patient will take a long time and hard work to recover afterwards.

Especially for weaker elderly patients, just a few days in bed could mean that they are not able to take care of themselves afterwards, with increased care expenses and increased risk of relapse as a consequence. Even though this is known, the work to motivate patients to be active during their hospitalization is limited to few training sessions with only the most vulnerable patients. No tools are today available for objectively tracking and motivating patients to be active during their stay. Having such a professional tool would not only motivate but also shift the attention of the health professionals towards the importance of physical activity in the treatment of the patient.

The aim of the studys is to investigate if patients hospitalised for medical disease will increase their time spent out of bed during hospitalisation through simple visual feedback about physical activities from a mobile bedside device.

Detailed Description

The study will be conducted as a quasi-randomised trial using a large tertiary public hospital in Copenhagen, Denmark. Patients admitted to Department of Respiratory Medicine (2 wards), Department of Cardiology, and Department of Geriatrics will be included, and they will have their physical activity level measured either with or without a bedside monitor providing visual feedback of time spent bedridden, sitting, standing and walking.

All participants will have their physical activity measured during hospitalisation. Approximately half of the participants will receive visual feedback about the amount of physical activity from a mobile device placed on the bedside table.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •An individual will be eligible for study participation if he/she meets the following criteria:
  • •Is admitted to one of the participating departments
  • •Has signed informed consent
  • •Reads and speaks Danish

Exclusion Criteria

  • •An individual will be excluded from the study if he/she meets any of the following criteria:
  • •Any condition that, in the opinion of the investigator, makes the person unfit for participation
  • •Expected hospitalisation less than 24 hours
  • •Has no independent ambulatory abilities (e.g. wheel chair user)
  • •Needs personal assistance in body transfers and ambulation (Cumulated Ambulation Score 0, 1, 2, or 3)
  • •Has allergy towards band aid

Arms & Interventions

Visual Feedback

Experimental

Participants in the intervention group will receive usual hospital care and be provided with a sensor collecting data on physical activity level during hospitalisation AND a monitor placed at their bedside that displays information about their physical activity level and motivation to move. This information will be visible to the health personnel, the patients and visitors.

Intervention: Physical activity measurement (Device)

Visual Feedback

Experimental

Participants in the intervention group will receive usual hospital care and be provided with a sensor collecting data on physical activity level during hospitalisation AND a monitor placed at their bedside that displays information about their physical activity level and motivation to move. This information will be visible to the health personnel, the patients and visitors.

Intervention: Visual Feedback (Device)

Control Group

Other

The participants in the non-exposed cohort will receive usual hospital care and be provided with a sensor collecting data on activity level during hospitalisation.No feedback on physical activity is provided.

Intervention: Physical activity measurement (Device)

Outcomes

Primary Outcomes

Time spent out of bed measured in minutes related to the total accelerometer wear time (minutes).

Time Frame: Through hospital stay, on average between 1 and 7 days

Secondary Outcomes

  • Time spent lying down, measured in minutes related to the total accelerometer wear time (minutes).(Through hospital stay, on average between 1 and 7 days)
  • Time spent walking measured in minutes related to the total accelerometer wear time (minutes).(Through hospital stay, on average between 1 and 7 days)
  • In-hospital fall incidents(Through hospital stay, on average between 1 and 7 days)
  • Readmission to hospital(within 90 days)
  • Time spent standing measured in minutes related to the total accelerometer wear time (minutes).(Through hospital stay, on average between 1 and 7 days)
  • Time spent sitting measured in minutes related to the total accelerometer wear time (minutes).(Through hospital stay, on average between 1 and 7 days)
  • Length of stay(Time from hospital admission to hospital discharge)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Marius Henriksen

Professor

Frederiksberg University Hospital

Study Sites (1)

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