Ireland
--:--IST
Recruiting Not applicable

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

NCT07500116 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2025-01-29
Last updated
2026-03-30

Condition(s) studied

Stroke (CVA) or TIAStroke Recurrence

Investigational drug(s) / intervention(s)

Home hospitalization

Home hospitalization: patients randomized to the treatment group (NORAHOME) to validate that our Home Hospitalization program for patients with TIA or minor stroke

Study summary

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.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: Patients presenting to the Emergency Department with symptoms of TIA (complete recovery of neurological deficits within \<24 hours) or minor stroke (NIHSS ≤ 5) * 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 Criteria: * Severe stenosis or symptomatic arterial occlusion requiring admission for potential reperfusion and/or arterial revascularization treatments. * 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.

Primary outcome measure(s)

  • Primary efficacy objective — 3months
    Change in the rate of early recurrence and hospital readmission compared to standard clinical practice.
  • Primary efficacy objective — 3 months
    Change in the rate of early recurrence and hospital readmission compared to standard clinical practice.
  • Primary safety objective — 3months
    Change in the number of complications (falls, recurrences, infections) in patients with TIA/minor stroke compared to standard clinical practice.

Trial sites (1)

FacilityCityRegionStatus
Vall Hebron University Hospital Barcelona Spain Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07500116 on ClinicalTrials.gov ↗ ← All trials in Spain