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Home-Based Monitoring for People With Minor Stroke or Transient Ischemic Attack

Tests whether home-based hospital care is safe for people with minor stroke or TIA.

Plain-language title generated from the registry record
Registry title: NORA-HOME: An Ambulatory Multimodal Monitoring Model In Patients With Minor Stroke And Transient Ischemic Attacks

Key facts

Where
Barcelona, SpainSee the site

Where in Spain

  • Vall Hebron University HospitalBarcelona, SpainTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Hospital Universitari Vall d'Hebron Research Institute
Trial code
NCT07500116
Record updated
30 March 2026
Original description
In this project, we aim to validate a Home Hospitalization plan for patients with TIA or minor stroke. Our hypothesis is that our Multimodal Home Hospitalization program (NORAHOME) for patients with TIA and minor stroke is safe, reduces the complications associated with conventional hospitalization, and is more efficient than Standard Clinical Practice. To conduct the study, we require the voluntary participation of patients with TIA and minor strokes.Read full original descriptionShow less

NORA-HOME. Efficiency And Safety An Ambulatory Multimodal Monitoring Model In Patients With Minor Stroke And Transient Ischemic Attacks

In this project, we aim to validate a Home Hospitalization plan for patients with TIA or minor stroke. Our hypothesis is that our Multimodal Home Hospitalization program (NORAHOME) for patients with TIA and minor stroke is safe, reduces the complications associated with conventional hospitalization, and is more efficient than Standard Clinical Practice. To conduct the study, we require the voluntary participation of patients with TIA and minor strokes.

Inclusion: Age >18 years; Availability of a smartphone for the patient or caregiver; Family support and/or formal caregiver; Clinical stability during the last 12 hours in the Emergency Department; Signed informed consent by the patient and/or family member or legal representative.

Exclusion: Patients with pre-existing neurological or psychiatric conditions that may interfere with or complicate follow-up and evaluations; Clinical (terminal condition) or social (language barrier) impossibility to complete follow-up assessments; Severe stenosis or symptomatic arterial occlusion requiring admission for potential reperfusion and/or arterial revascularization treatments.

ClinicalTrials.gov NCT07500116