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NCT07524036Recruiting

Impact of a Nursing Educational Consultation on the Patient's Adherence to Their Post-stroke Care Plan.

Impact of a Nursing Consultation at the End of Hospitalization on Adherence to the Post-stroke Care Plan for Patients Admitted to the Vascular Neurology Unit

Source: ClinicalTrials.gov · Last updated 18 Aug 2026

Brief summary (registry, in English)

This prospective, single-center, randomized study will evaluate the impact of implementing an educational nursing consultation at the end of hospitalisation for stroke patients returning home on overall adherence to stroke-related medication during the 4-month follow-up visit.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
300 (estimated)
First submitted
23 Mar 2026
Start date
Jun 2026
Primary completion date
Jun 2028
Lead sponsor
University Hospital, Bordeaux
Diseases
Stroke
NCT number
NCT07524036

What you commit to

  • Study type: Interventional
  • Planned participants: 300
  • From Jun 2026 to the primary completion date, Jun 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients requiring assistance from a third party at home for the management of their medication or with stroke follow-up at Prado

Other

  • Patients admitted for mechanical thrombectomy, outside the Basque Coast Hospital (CHCB)
  • Rankin score estimated at discharge ≥ 4
  • Patients placed under protection measures

Who the study is looking for

  • Patients admitted to the Neurovascular Unit (UNV) of CHCB for ischemic stroke and/or hemorrhagic stroke confirmed by brain imaging and/or TIA with an ABCD2 score \>5,
  • Patients whose discharge orientation is a return home
  • Age ≥ 18 years
  • NIHSS \< 15
  • Montreal Cognitive Assessment (MoCa) \> 21/30
  • Free and informed consent signed by the patient.
  • Person affiliated with or a beneficiary of a social security scheme

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier de la Cote Basque
Coordinator of this site? Confirm its status
BayonneFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.