NL-OMON51649已完成不适用
Effectiveness of Hospital Fit on physical activity of hospitalised patients: a stepped-wedge cluster-randomised clinical trial and process evaluation. - Effectiveness of Hospital Fit
Medisch Universitair Ziekenhuis Maastricht0 个研究点目标入组 180 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 180
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Inclusion criteria patients (n<=180):
- •In order to be eligible to participate in this study, a patient must meet all
- •the following criteria:
- •* Over 18 years old.
- •* Receiving physiotherapy at the Medical Oncology department or the Cardiology
- •department at the MUMC+ or Radboudumc.
- •* Enough understanding of the Dutch language.
- •* Owning a smartphone (operating system * iOS13.0 or Android 8.0)
- •* Able to use a smartphone app
- •* Able to walk independently 2 weeks before admission, as scored on the
- •Functional Ambulation Categories (FAC >3)
- •Inclusion criteria healthcare professionals (n<=24):
- •In order to be eligible to participate in the focus group interviews of the
- •proces-evaluation, a healthcare professional must meet all the following
- •* Employed as physiotherapist, nurse or physician (assistant) at the Medical
- •Oncology Department or the Cardiology Department.
- •* Working at the MUMC+ or Radboudumc for at least one month.
排除标准
- •Exclusion criteria patients:
- •A potential subject who meets any of the following criteria will be excluded
- •from participation in this study:
- •* A contraindication to walking (as reported by a medical specialist in the
- •electronic medical record).
- •* A contraindication to wearing an activity monitor, fixed by a hypoallergenic
- •plaster at the upper leg (such as active bilateral upper leg infection, severe
- •oedema or bilateral transfemoral amputation).
- •* Admitted for cancers of the head and neck (i.e., cancer in the oral cavity,
- •throat (pharynx), voice box (larynx), paranasal sinuses and nasal cavity,
- •salivary glands).
- •* Admitted with cardiac arrhythmia and hemodynamic instability requiring
- •medication over 48 hours (i.e., beta blockers or noradrenaline) or invasive
- •treatment (i.e., pacemaker or defibrillator implementation).
- •* Mentally incapacitated subjects as reported by healthcare professionals in
- •the medical record. When any doubt arises, the patient will be excluded.
- •* Impaired cognition (delirium / dementia) as reported in the medical record by
- •a healthcare professional. When any doubt arises, the patient will be excluded.
- •* Unable to participate in the informed consent procedure or unable to provide
- •written informed consent.
- •* A life expectancy shorter than 3 months as mentioned by the medical
- •specialist in the medical record.
- •* Previous participation in this study.
- •Exclusion criteria healthcare professionals:
- •* No participation in care for patients at the Medical oncology Department or
- •Cardiology Department during the intervention phase (e.g., absence or research
- •employment).
研究者
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