跳至主要内容
临床试验/NL-OMON56103
NL-OMON56103招募中不适用

To determine the effectiveness of the RISE intervention on preventing major adverse cardiovascular effects (MACE), after discharge from acute hospital care in community dwelling people after first-ever stroke, who have a sedentary movement behavioural pattern. In addition, the effects on 24h activity pattern, cost-effectiveness, and usability of the RISE intervention will be investigated. - RISE intervention

niversitair Medisch Centrum Utrecht0 个研究点目标入组 1,200 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
招募中
发起方
入组人数
1,200

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

  • In order to be eligible, a subject must meet all of the following criteria:
  • 1. Aged 18 years or older;
  • 2. All types of stroke diagnosed in hospital within six months before start of
  • the RISE intervention;
  • 3. Able to walk independently, as defined by a Functional ambulation categories
  • score of at least 3;
  • 4. Independent regarding activities of daily living pre-stroke, as defined by a
  • Barthel Index score of >18;
  • 5. Discharged to the home-setting;
  • 6. Not participating in a physiotherapeutic traject lasting >= 3 months, as
  • determined by the physiotherapist in charge.
  • 7. Given their written informed consent.

排除标准

  • A potential subject will be excluded from participation in this study if:
  • 1. The participant is (cognitively) not capable of understanding the
  • intervention content;
  • 2. The participant has severe comorbidities that withhold 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);

研究者

发起方
niversitair Medisch Centrum Utrecht

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