Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
290 participants
INTERVENTIONAL
2014-01-30
2021-12-16
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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optimised follow-up
optimised follow-up will be done by nursing personnel associated with a caregiving member of his social circle.
optimised follow-up
optimised follow-up will be done by nursing personnel associated with a caregiving member of his social circle.
typical follow-up
no intervention
No interventions assigned to this group
Interventions
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optimised follow-up
optimised follow-up will be done by nursing personnel associated with a caregiving member of his social circle.
Eligibility Criteria
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Inclusion Criteria
* 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 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
60 Years
90 Years
ALL
No
Sponsors
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Ministry of Health, France
OTHER_GOV
University Hospital, Lille
OTHER
Responsible Party
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Principal Investigators
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REGIS BORDET, MD phD
Role: PRINCIPAL_INVESTIGATOR
University Hospital
Locations
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Chu Amiens Picardie
Amiens, , France
CHU
Besançon, , France
CHU
Bordeaux, , France
Chru Brest
Brest, , France
Hopital Pierre Wertheimer - Hcl
Bron, , France
CH
Calais, , France
Samsah Ghicl Capinghem
Capinghem, , France
Ch Intercommunal Compiègne-Noyon - Compiegne
Compiègne, , France
CHU
Dijon, , France
Chu de Grenoble Alpes - Grenoble 9
Grenoble, , France
CHRU
Lille, , France
C H U Dupuytren Limoges
Limoges, , France
Ch Sambre Avesnois Maubeuge
Maubeuge, , France
Ch Saint Joseph
Paris, , France
Chu La Miletrie - Poitiers
Poitiers, , France
CHU
Rouen, , France
Chru Nancy - Hopitaux de Braboi
Vandœuvre-lès-Nancy, , France
Countries
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References
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Mendyk AM, Duhamel A, Bejot Y, Leys D, Derex L, Dereeper O, Detante O, Garcia PY, Godefroy O, Montoro FM, Neau JP, Richard S, Rosolacci T, Sibon I, Sablot D, Timsit S, Zuber M, Cordonnier C, Bordet R; on the behalf of Strokavenir network. Controlled Education of patients after Stroke (CEOPS)- nurse-led multimodal and long-term interventional program involving a patient's caregiver to optimize secondary prevention of stroke: study protocol for a randomized controlled trial. Trials. 2018 Feb 22;19(1):137. doi: 10.1186/s13063-018-2483-0.
Crocker TF, Brown L, Lam N, Wray F, Knapp P, Forster A. Information provision for stroke survivors and their carers. Cochrane Database Syst Rev. 2021 Nov 23;11(11):CD001919. doi: 10.1002/14651858.CD001919.pub4.
Other Identifiers
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2012-A00473-40
Identifier Type: OTHER
Identifier Source: secondary_id
PHRIP 2012 - N°12-019-0306
Identifier Type: OTHER
Identifier Source: secondary_id
2011_34
Identifier Type: -
Identifier Source: org_study_id
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