Controlled Education Of Patients After Stroke

Not Applicable

• Conditions: Hypertension; Stroke
• Interventions: Other: optimised follow-up

• Registration Number: NCT02132364
• Lead Sponsor: University Hospital, Lille

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2014-01-30
• Study First Submitted: 2014-05-05
• Study First Submitted QC: 2014-05-06
• Study First Posted: 2014-05-07
• Status Verified: 2020-08
• Last Update Submitted: 2020-09-08
• Last Update Posted: 2020-09-09
• Primary Completion: 2021-07
• Study Completion: 2021-07

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 800

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

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

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

Primary Outcome Measures

Name	Time	Method
blood pressure	12 months	blood pressure will be measured by nursing personnel who do not know the group into which the patient has been randomised.

Secondary Outcome Measures

Name	Time	Method
Outcome of stroke	6 months 12 months 2 years.	functional handicap (Rankin scale) cognitive state (MoCA scale)

Trial Locations

Locations (14)

Ch Saint Joseph; 🇫🇷 Paris, France

Chu La Miletrie - Poitiers; 🇫🇷 Poitiers, France

Ch Sambre Avesnois Maubeuge; 🇫🇷 Maubeuge, France

Chru Brest; 🇫🇷 Brest, France

Chu Amiens Picardie; 🇫🇷 Amiens, France

Ch Intercommunal Compiègne-Noyon - Compiegne; 🇫🇷 Compiègne, France

CHU; 🇫🇷 Rouen, France

Chru Nancy - Hopitaux de Braboi; 🇫🇷 Vandœuvre-lès-Nancy, France

Samsah Ghicl Capinghem; 🇫🇷 Capinghem, France

CHRU; 🇫🇷 Lille, France

Hopital Pierre Wertheimer - Hcl; 🇫🇷 Bron, France

CH; 🇫🇷 Calais, France

Chu de Grenoble Alpes - Grenoble 9; 🇫🇷 Grenoble, France

C H U Dupuytren Limoges; 🇫🇷 Limoges, France