← Eichor
Study identifier: NCT06124248 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effectiveness of the RISE Intervention

Condition: Sedentary Behaviour · Stroke  ·  Sponsor: UMC Utrecht

PhaseNA
Planned participants1000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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 usual care, at the end of the intervention period (T1). For this aim, 59 persons are enrolled in the experimental group and 59 in the control group. Considering loss to follow up, it is expected that around 197 patients need to be included during baseline measurement in total. Who can participate? People aged over 18, who return home after acute care with a first-ever stroke, who are independent in walking with or without a walking aid, will be included in the RISE intervention study. What does the study involve? In this clinical randomized controlled trial, participants with first-ever stroke a…

This description comes directly from the study's public registry record.

Talk to the study team

Martijn F Pisters, Dr.  ·  +31 6 43 042 462  ·  m.f.pisters@umcutrecht.nl

Camille FM Biemans  ·  +31 6 13218777  ·  c.f.m.biemans@umcutrecht.nl

Always discuss trial participation with your own doctor first.

Locations (21)

Fysio 4 Den Bosch's-Hertogenbosch, North Brabant, NetherlandsRecruiting
Meras & Vital FysiotherapieEersel, North Brabant, NetherlandsRecruiting
PMC EindhovenEindhoven, North Brabant, NetherlandsRecruiting
Stroomz PrinsejagtEindhoven, North Brabant, NetherlandsRecruiting
Fysiotherapie ZesgehuchtenGeldrop, North Brabant, NetherlandsRecruiting
JVDI De FysioclubHelmond, North Brabant, NetherlandsRecruiting
Fysiotherapie RakthofHelmond, North Brabant, NetherlandsRecruiting
ViventRosmalen, North Brabant, NetherlandsRecruiting
Van Hoof, centrum voor therapie en gezondheidValkenswaard, North Brabant, NetherlandsRecruiting
Fysio Annette de GooijerVlijmen, North Brabant, NetherlandsRecruiting
Fysiofit VughtVught, North Brabant, NetherlandsRecruiting
Fysio Vught NoordVught, North Brabant, NetherlandsRecruiting

+ 9 more locations — full list on the registry record.

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06124248