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Nurse coaching after stroke: does it lower blood pressure?

NCT ID NCT02132364

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether stroke patients over 60 with high blood pressure benefit from extra nurse-led education and follow-up, compared to standard care. About 290 patients took part, each bringing a family member or friend to help. The main goal was to see if this approach lowers blood pressure better than usual follow-up.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

290 people

The number who actually took part.

Started

Jan 2014

Finished

Dec 2021

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

60 to 90 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • C H U Dupuytren Limoges

    Limoges, France

  • CH

    Calais, 62100, France

  • CHRU

    Lille, 59037, France

  • CHU

    Bordeaux, 33076, France

  • CHU

    Dijon, 21000, France

  • CHU

    Rouen, 76031, France

  • CHU

    Besançon, 25000, France

  • Ch Intercommunal Compiègne-Noyon - Compiegne

    Compiègne, France

  • Ch Saint Joseph

    Paris, 75674, France

  • Ch Sambre Avesnois Maubeuge

    Maubeuge, France

  • Chru Brest

    Brest, France

  • Chru Nancy - Hopitaux de Braboi

    Vandœuvre-lès-Nancy, France

  • Chu Amiens Picardie

    Amiens, France

  • Chu La Miletrie - Poitiers

    Poitiers, France

  • Chu de Grenoble Alpes - Grenoble 9

    Grenoble, France

  • Hopital Pierre Wertheimer - Hcl

    Bron, France

  • Samsah Ghicl Capinghem

    Capinghem, France

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