Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06995040

Initial Predictors of Long-term Brain Resilience After Minor Ischemic Stroke: a Study Nested in the Brest Stroke Population-based Registry

Led by University Hospital, Brest · Updated on 2026-02-23

1000

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to develop a predictive model for quality of life more than four years after a minor ischemic stroke. It focuses on patients with mild stroke deficits, defined by a National Institute of Health Stroke Scale (NIHSS) score of 5 or less, to better understand long-term outcomes. The study will analyze both retrospective and prospective data from the Brest Stroke Registry, including patient characteristics collected shortly after stroke onset. Participants include patients who suffered a minor ischemic stroke over four years ago and are part of the Brest Stroke Registry. They may take part through telephone or face-to-face interviews with neurologists and clinical research technicians. Optional procedures include providing a saliva sample for DNA analysis and undergoing a cerebral MRI without contrast. The study will use questionnaires to assess quality of life and cognitive function, with data linked from hospital records and the registry. During the study, participants will complete quality of life and cognitive questionnaires and may provide saliva samples and have an MRI scan. Researchers will measure various outcomes such as quality of life scores, cognitive assessments, disability scales, depression and anxiety screening, and stroke recurrence. The study includes over four years of follow-up, with data collected at inclusion and the possibility of long-term monitoring of brain resilience after minor ischemic stroke.

CONDITIONS

Brief Title

BREMISS : Brain Resilience Minor Stroke Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Cases of stroke in the Brest Stroke Registry
  • Ability to sign informed consent
  • Patients followed-up more than 4 years during the study period
  • NIHSS score 5 or less on admission
  • First stroke between 18 and 75 years old
  • Rankin score before stroke less than 1
  • Possibility to provide saliva samples for genomic study
  • Possibility to perform cerebral MRI
Not Eligible

You will not qualify if you...

  • Patients with transient neurological deficits resolving within one hour and normal brain imaging
  • Not affiliated to social security
  • Patient under legal protection or deprived of liberty by judicial or administrative decision
  • Patient unable to sign informed consent
  • Patient whose follow-up will be impossible

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or by telephone)

Diagnostic Evaluation

Duration - 1 day

Participants undergo cerebral MRI and provide saliva samples for DNA analysis either during a face-to-face visit or by sending samples from home. Additionally, quality of life and cognitive questionnaires are completed.

1 visit (in-person) or home sample collection

Long-term Monitoring

Duration - More than 4 years

Participants’ long-term brain resilience and quality of life are observed more than 4 years after minor ischemic stroke, based on retrospective and prospective data collection.

1 telephone or face-to-face follow-up interview

Trial Site Locations

Total: 1 location

1

CHU de Brest

Brest, France, 29609

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Research Team

S

Serge TIMSIT, Pr

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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