Skip to content

Controlled Education Of Patients After Stroke

Controlled Education Of Patients After Stroke

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02132364
Acronym
CEOPS
Enrollment
290
Registered
2014-05-07
Start date
2014-01-30
Completion date
2021-12-16
Last updated
2025-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension, Stroke

Keywords

stroke, hypertension, secondary prevention, educational program

Brief summary

The main objective of the study is to compare the benefit of optimised follow-up by nursing personnel from the vascular neurology department, including therapeutic follow-up and an educational program directed to the patient and a caregiving member of his social circle, with that of a typical follow-up.

Interventions

OTHERoptimised follow-up

optimised follow-up will be done by nursing personnel associated with a caregiving member of his social circle.

Sponsors

Ministry of Health, France
CollaboratorOTHER_GOV
University Hospital, Lille
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Patients over 60 years of age * Patients who have had a first stroke, transient or permanent, ischaemic or haemorrhagic, justifying hospitalisation * Patients with high blood pressure already treated or discovered at the time of the stroke and justifying the start of a treatment * Patients who have had a stroke with sequelae allowing immediate return home or justifying a stay of less than one month in rehabilitation * Patient having a member of his social circle who has agreed to provide follow-up for two years in association with the assigned nursing personnel in case of randomisation into the optimised follow-up group.

Exclusion criteria

* Patients less than 60 years of age * Patients with a history of stroke * Patients who do not have high blood pressure discovered by a treatment prior to the stroke or by abnormal blood pressure figures during hospitalisation * Patients who have had a stroke causing serious sequelae, justifying an extended stay in a rehabilitation department * Patient who has no one in his social circle capable of working with the assigned nursing personnel, or patient living in an institution

Design outcomes

Primary

MeasureTime frameDescription
blood pressure12 monthsblood pressure will be measured by nursing personnel who do not know the group into which the patient has been randomised.

Secondary

MeasureTime frameDescription
Outcome of stroke6 months 12 months 2 years.functional handicap (Rankin scale) cognitive state (MoCA scale)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026