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
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