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临床试验/NL-OMON55033
NL-OMON55033已完成不适用

Preliminary effectiveness and feasibility of the RISE intervention to reduce and interrupt sedentary behaviour in community dwelling sedentary people after stroke. - RISE intervention

niversitair Medisch Centrum Utrecht0 个研究点目标入组 12 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
12

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

  • 1. Aged 18 years or older;
  • 2. Stroke diagnosed in hospital within six months of the start of the RISE
  • intervention;
  • 3. Able to walk independently, as defined by a Functional ambulation categories
  • score of at least 3;
  • 4. Sedentary prolonger; i.e. *9.5 hours of sedentary time per day and meeting
  • at least one of the following criteria: >50% of the sedentary time is spent in
  • bouts > 30 minutes and not reaching the physical activity guideline (150
  • minutes MVPA during the week);
  • 5. Independent regarding activities of daily living pre-stroke, as defined by a
  • Barthel Index score of >18;
  • 6. Discharged to the home-setting;
  • 7. Have someone who can participate as a bubby in the RISE intervention with
  • 8. Given their written informed consent.

排除标准

  • 1. Insufficient knowledge of the Dutch language to understand the intervention
  • 2. Score <4 on the Utrecht Communication Assessment (UCO) to understand
  • questionnaires and follow instructions;
  • 3. Severe comorbidities that prevent that person from safely reducing and
  • interrupting their sedentary time (e.g. sever pulmonary diseases, hart failure
  • or malignity*s) as determined with the Physical Activity Readiness
  • Questionnaire (PAR-Q);
  • 4. Not receiving physiotherapy in any other setting then primary care.

研究者

发起方
niversitair Medisch Centrum Utrecht

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