Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06187025

Addiction & Stroke

Led by University Hospital, Bordeaux · Updated on 2025-07-20

300

Participants Needed

1

Research Sites

182 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Modifiable stroke risk-factors, which include poor lifestyle habits, account for 90 % of the risk of stroke. Disability Adjusted Life Years (DALYs) related to cerebrovascular disorders rely on three main factors, including the severity of stroke-related symptoms, the occurrence of stroke complications, and stroke recurrences. Stroke complications and the risk of stroke recurrence are highly dependent on the control of vascular risk factors. Thus, the secondary prevention of stroke involves profound lifestyle modifications including substance use cessation and diet changes.

CONDITIONS

Official Title

Addiction & Stroke

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female
  • At least 18 years of age and younger than 80 years
  • Recent (\u2264 15 days) clinically symptomatic ischemic or hemorrhagic stroke documented by brain imaging (CT or MRI) or Transient Ischemic Attack with an ABCD2 score \u2265 4
  • Returning to Bordeaux Hospital neurovascular unit for standard 3-month post-stroke follow-up
  • National Institute Health Stroke Scale (NIHSS) less than 15
  • Modified Rankin scale \u2264 4
  • No severe cognitive impairment as defined by neurologist
  • Written informed consent by patient
  • Coverage by French National Health Insurance
  • For the eHealth feasibility study: ability to use a smartphone and live in an area with internet coverage
Not Eligible

You will not qualify if you...

  • Subarachnoid hemorrhage
  • Dementia syndrome or other neurologic disorder
  • Severe aphasia (NIHSS item 9 \u2265 2) and/or severe visual impairment interfering with evaluations
  • Severely impaired physical and/or mental health affecting participation
  • Pregnancy or breastfeeding
  • Inability to read French
  • Under legal protection or unable to personally consent
  • Participation in another protocol modifying follow-up status

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU de Bordeaux

Bordeaux, France, 33076

Actively Recruiting

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Research Team

I

Igor Sibon

CONTACT

S

Sylvie Berthoz

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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