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Controlled Education Of Patients After Stroke (CEOPS)

U

University Hospital, Lille

Status

Completed

Conditions

Hypertension
Stroke

Treatments

Other: optimised follow-up

Study type

Interventional

Funder types

Other

Identifiers

NCT02132364
2011_34
2012-A00473-40 (Other Identifier)
PHRIP 2012 - N°12-019-0306 (Other Identifier)

Details and patient eligibility

About

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.

Enrollment

290 patients

Sex

All

Ages

60 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

290 participants in 2 patient groups

optimised follow-up
Other group
Description:
optimised follow-up will be done by nursing personnel associated with a caregiving member of his social circle.
Treatment:
Other: optimised follow-up
typical follow-up
No Intervention group
Description:
no intervention

Trial contacts and locations

17

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Central trial contact

Regis BORDET, MD phD

Data sourced from clinicaltrials.gov

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