Increasing Physical Activity Among Medical Inpatients by Digital Nudging of Patients and Staff - A Cluster Randomised Multicentre Study
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 400
- 试验地点
- 4
- 主要终点
- Daily average time of participants' physical activity (minutes)
研究概览
简要总结
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).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Admitted to one of the participating wards
- •Has understood and signed informed consent
- •Reads and understands Danish, Faroese, Greenlandic or English
排除标准
- •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.
结局指标
主要结局
Daily average time of participants' physical activity (minutes)
时间窗: From enrollment to end of trial participation (maximum 7 days)
次要结局
未报告次要终点
研究者
Christian Dall
Associate professor
Bispebjerg Hospital