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

Bispebjerg Hospital

Status: Enrolling

Conditions: Inpatients; Physical Activity; Digital Health

Treatments: Other: Digital nudging; Other: Measurement of physical activity

Study type: Interventional

Funder types: Other

Identifiers

NCT06983977

VMK-2403916

Details and patient eligibility

About

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).

Enrollment: 400 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Admitted to one of the participating wards
• Has understood and signed informed consent
• Reads and understands Danish, Faroese, Greenlandic or English

Exclusion criteria

• 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

• There are contraindications for the patient to mobilise or be physically active due to unstabilized acute medical conditions, including, but not limited to, acute aortic dissection, -myocardial infarction, -pulmonary embolism, -sepsis.

• There are ethical concerns regarding the patients' participation in the study, including, but not limited to, the patient being:

  • In the terminal phase of life
  • In a crisis state regarding their disease/situation and deemed unfit for participation

To ensure medically responsible inclusion of patients, the project personnel will consult and confer with the treatment responsible medical doctor, or their delegate, before including a potential participant for the trial.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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400 participants in 2 patient groups

Control

Other group

Description:

Measurement of physical activity

Treatment:

Other: Measurement of physical activity

Intervention

Experimental group

Description:

Digital feedback and nudging to participant and staff regarding participants' physical activity levels

Treatment:

Other: Digital nudging