AI Cure is a research tool showing open data. Not medical advice. Discuss with your doctor. Terms

โ† Trials
๐Ÿงช

Effectiveness of the RISE Intervention

RecruitingNAAges 18 Years - anyAllUMC Utrecht
๐Ÿ’ฌ

In plain words

What the trial is, and whether it could suit you

Study aim: Primarily, to investigate the effectiveness of the RISE blended behaviour change intervention in people with a first stroke to prevent major adverse cardiovascular events (i.e., recurrent stroke or TIA, acute coronary events and cardiovascular death, MACE) after 1 year follow-up compared to standard care, and cost-effectiveness. For this aim, 376 persons are enrolled in the experimental group and 376 in the control group. Considering loss to follow up, it is expected that around 950-1000 patients need to be included during baseline measurement in total. Additionally, to determine the effectiveness of the RISE intervention on reducing sedentary behaviour after discharge from acute hospital care in community dwelling people with a first-ever stroke, who have a sedentary movement behavioural pattern (so called 'sedentary prolongers' and 'sedentary movers') in comparison to usua

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: In order to be eligible to participate in the baseline measurement of the intervention study, a subject must meet all of the following criteria: 1. Aged 18 years or older; 2. All types of first-ever 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 physical rehabilitation program lasting โ‰ฅ 3 months; 7. Given their written informed consent. Exclusion Criteria: A potential subject will be excluded from participation in this study if: 1. The participant has insufficient knowledge or is cognitively unable to understand the Dutch language of 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;
๐Ÿ’Š

What it tests

  • RISE intervention
๐Ÿ“

Where

21 sites
Fysio 4 Den Bosch
's-Hertogenbosch, Netherlands
Meras & Vital Fysiotherapie
Eersel, Netherlands
PMC Eindhoven
Eindhoven, Netherlands
Stroomz Prinsejagt
Eindhoven, Netherlands
Fysiotherapie Zesgehuchten
Geldrop, Netherlands
JVDI De Fysioclub
Helmond, Netherlands
Fysiotherapie Rakthof
Helmond, Netherlands
Vivent
Rosmalen, Netherlands

โ€ฆand 13 more on ClinicalTrials.gov.

๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
๐Ÿ›ก๏ธ

AI Cure shows public evidence (Open Targets, ClinicalTrials.gov, PubMed, openFDA, DepMap, AlphaFold) with its source, and AI summaries that cite it โ€” not medical advice and not a cure. Treatment decisions belong with your doctor. Research ideas are shared only with approved researchers and labs, who can test them. In an emergency call your local emergency number (112 in India and Europe, 911 in the US). AI Cure Terms of Use ยท Privacy