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The effect of a smartphone app with accelerometer on patients* physical activity: a randomised controlled trial.

The effect of a smartphone app with accelerometer on patients* physical activity: a randomised controlled trial. - Hospital Fit 2.0 - RCT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON51887
Enrollment
78
Registered
2020-12-16
Start date
2021-03-23
Completion date
Unknown
Last updated
2024-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low physical activity: low mobility

Interventions

All subjects eligible for inclusion in this study receive usual care physiotherapy as prescribed by the physician and receive an accelerometer, measuring PA, which is attached by the physiotherapist

Sponsors

Medisch Universitair Ziekenhuis Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Aged 18 to 75 years. • Receiving physiotherapy while hospitalised at the department of Internal Medicine department or the department of Pulmonology at the Maastricht University Medical Centre (MUMC+) • Sufficient understanding of the Dutch language • Having access to a smartphone • Able to walk independently 2 weeks before admission, as scored on the Functional Ambulation Categories (FAC >3)

Exclusion criteria

Exclusion criteria: • A contraindication to walking (as reported by the attending medical specialists in the medical record) • A contraindication to wearing an accelerometer, fixed by a hypoallergenic plaster at the upper leg (such as active bilateral upper leg infection, severe edema or bilateral transfemoral amputation) • Admission at the intensive care department • Impaired cognition (delirium / dementia) as reported by the attending doctor • 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 • Previous participation in this study

Design outcomes

Primary

MeasureTime frame
The primary outcome parameters is time spent walking per day (min.)

Secondary

MeasureTime frame
The secondary outcome parameters are: - Average time spent walking (defined as the total number of minutes walking divided by the total number of valid measurement days in the period between inclusion and discharge, with a maximum of seven days). - Time spent standing per day (min.) - Average time spent standing (defined as the total number of minutes standing divided by the total number of valid measurement days in the period between inclusion and discharge, with a maximum of seven days). - Number of transitions from a sedentary position (lying or sitting) to an active position (standing or walking) per day - Average number of transitions from a sedentary position (lying or sitting) to an active position (standing or walking) (defined as the total number of transitions divided by the total number of valid measurement days in the period between inclusion and discharge with a maximum of seven days). The following medical and demographic data are collected from the electronic medical record: - Age (years) - Gender (male/female) - Clinical diagnosis - Walking aid (e.g. walker, crutches) - Length of stay (days) - Discharge location (e.g. home, rehabilitation clinic) - Number of physiotherapy treatment sessions received between inclusion and discharge

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)