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Transient Ischemic AttackLitterAITNCT07040761

Medical Literacy in TIA (Transient Ischemic Attack) Patients

An observational study of Transient Ischemic Attack, run by Hospices Civils de Lyon at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

There are around 30,000 TIAs (transient ischemic attacks) per year in France. This pathology can be the warning sign of a stroke, responsible for significant morbidity and mortality at the population level. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Transient Ischemic Attack
What is being tested?
Two medical questionnaires
How many people
100 participants
Where
1 siteFrance
Study dates
30 Jun 2025to 5 Dec 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients from the Lyon region who consulted an emergency department with a final diagnosis of TIA, and sent to the neurology day hospital of Pierre Wertheimer neurological hospital

Who may be able to join

  • Adult men and women ≥18 years old
  • Patient referred to neurology day hospital at the Pierre Wertheimer neurological hospital after first care in the emergency department
  • Patient having been informed and having expressed his non-opposition
  • Patient affiliate to a social security scheme

Who cannot join

  • Patient unable to complete the questionnaire
  • History of stroke/TIA
  • Patient who do not understand the French language
  • Patient under legal protection, guardianship, curatorship, under judicial protection-

Trial locations and contacts

1 site in 1 country.

France1 site
  • Pierre Wertheimer hospital

    Bron

Other trials in France

About this study

Official title: Evaluation of Medical Literacy in Patients Who Presented With a TIA Treated in Emergency Departments in Lyon

There are around 30,000 TIAs (transient ischemic attacks) per year in France. This pathology can be the warning sign of a stroke, responsible for significant morbidity and mortality at the population level.

An important part of patient care is to teach them to recognize the symptoms suggestive of a stroke as well as the contributing factors, thus improving the medical literacy of patients.

Read more

The results of studies that have assessed medical literacy in France and Europe converge towards a rather low level.

Some studies have focused on stroke literacy in France. They show good knowledge of risk factors and the attitude to adopt in the event of a stroke, but recognition of symptoms remains problematic.

There is very little literature concerning knowledge of TIA in the general population and there are no studies concerning literacy in a population having presented with TIA.

The aim of this study is to evaluate the knowledge of patients who have presented with a TIA (and therefore at high cardiovascular risk) about this disease (risk factors, symptoms, severity, attitude to adopt in the event of symptoms), after their visit to the emergency room.

The investigators make the hypothesis that knowledge of TIA and its consequences will be rather low in this population of patient, even after a medical contact at the emergency room.

Being tested
Two medical questionnaires
Keywords
Transient ischemic attack, Medical literacy, Emergency department
Medical subject headings
Ischemic Attack, Transient, Emergencies

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Two medical questionnairesOther

    Medical questionnaires delivered by hand and completed the same day

Study groups in NCT07040761
Study groupRoleWhat they receive
TIATIA patients diagnosed in the emergency department and sent to neurology day hospital for evaluation
Receives: Other: Two medical questionnaires

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Quality of responses to the medical literacy questionnaire specific to TIAs

    The questionnaire contains 18 questions, open or closed. Each question will be analysed separately and the results will be expressed as a percentage of correct answer (in the case of a closed question mainly) or by specifying the different answers provided by the patients (in the case of an open question mainly)

    Measured: Day 1 at inclusion

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Jun 2025
  2. Study start30 Jun 2025
  3. Primary completion5 Dec 2025
  4. Study completion5 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07040761
Sponsor's protocol ID
69HCL25_0091
Other IDs
2025-A00239-40
Acronym
LitterAIT
Status last verified
Dec 2025
First submitted
18 Jun 2025
Last updated
19 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Transient Ischemic Attack, run by Hospices Civils de Lyon at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Quality of responses to the medical literacy questionnaire specific to TIAs (time frame: Day 1 at inclusion). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Dec 2025.

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