Increasing Physical Activity Among Medical Inpatients by Digital Nudging of Patients and Staff

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorBispebjerg Hospital

About this trial

Sedentary behaviour among medical inpatients is strongly associated with hospital-associated functional decline and poses a severe threat to patients' functional capacity and independency. High human and socioeconomic costs underline the urgency to find solutions to this world-wide problem.

Objective: This multicentre study, including a total of 400 patients from Copenhagen, Aalborg, Tórshavn, and Nuuk, will assess the effect of a digital intervention that aims to reduce sedentary behaviour and increase physical activity in medical inpatients.

Intervention: Digital feedback and nudging regarding the patients' physical activity levels to patients and healthcare staff Design: Stepped-wedge cluster randomised multicentre trial Primary outcome: Daily average time of patients' physical activity (minutes).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Admitted to one of the participating wards

Has understood and signed informed consent

Reads and understands Danish, Faroese, Greenlandic or English

Disqualifiers

Has an expected hospitalisation less than 24 hours after potential recruitment

Is not able to give informed consent to participate in the study

Has allergy towards band aid

Not able to (shortly) stand in an upright position even with maximal assistance

Trial design

Design model

Parallel

Treatments tested in this trial

  • Measurement of physical activity

    Other intervention

    Measurement of physical activity by accelerometer

  • Digital nudging

    Other intervention

    Digital feedback and nudging to participants (patients) and staff, based on participants' physical activity measurements, aiming to increase patients' physical activity and reduce sedentary time

Treatment groups

400 Participants
are divided into 2 treatment groups
Group A: ControlOther 1 intervention
Group B: InterventionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Daily average time of participants' physical activity (minutes)

Time frame
From enrollment to end of trial participation (maximum 7 days)

Secondary outcomes

Other outcomes

Sponsors and contacts

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