- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03975218
Involvement of the Physician in Primary Prevention and Pre-hospital Management of Stroke (PREVENTION AVC)
Stroke is a growing disease. It is the first pathology responsible for acquired handicap, the second of dementia and the second cause of death in the world. In France, they are the leading cause of death in women and the third cause in men. Sequelae and disabilities also represent a significant financial cost for health insurance.
The early management of the treatment improves the patient's vital and functional prognosis. The ability of the patient to identify the signs of stroke requiring urgent consultation and proper orientation are therefore crucial for further management.
The most common signs that patients must recognize are muscle weakness or sudden paralysis of an arm, leg or half of the body, asymmetry of the face, tingling, numbness of a hemi-body, speech or understanding, loss of vision of an eye or hemifield, disorder of the coordination of a hemi-body. The variety of clinical pictures complicates primary prevention.
In this context, a 2010-2014 National Stroke Action Plan was undertaken with the aim, among other things, of developing information to prevent stroke and to limit its sequelae. In this plan, the attending physician must improve prevention in high-risk patients and be a link between the city and the hospital for follow-up.
Several questions arise:
- Are patients who are regularly followed by a general practitioner better educated on the signs of stroke / TIA and thus more able to give an appropriate warning?
- What is the profile of patients who have not been affected by the different modes of primary prevention?
- What are the effective means of information and those desired
Study Overview
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Paris, France, 75014
- Groupe Hospitalier Paris Saint-Joseph
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patient whose age is ≥ 18 years
- Patient hospitalized in the neurology / neurovascular department within the GHPSJ following a stroke (first episode or recurrence)
- Francophone patient
Exclusion Criteria:
- Patient with previously labeled cognitive impairment
- Patient under tutorship or curatorship
- Patient deprived of liberty
- Patient unable to answer the questionnaire
- Patient opposing participation in the study
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Patients with stroke
In addition to the usual care, the patient will have to complete a questionnaire analyzing the regularity of his follow-up by a physician.
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In addition to the usual care, the patient will have to complete a questionnaire analyzing the regularity of his follow-up by a physician.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time until patient's care in the hospital after stroke's symptoms
Time Frame: Day 1
|
The delay between the observation of signs of stroke and specialized neurovascular management at the hospital will be measured.
This measures the impact of physician's prevention on the management of stroke.
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Day 1
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Study the different effective means of primary prevention
Time Frame: Day 1
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Patient questionnaire corresponds to open question about physician in primary prevention and pre-hospital management of stroke to which the patient will respond yes or no.
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Day 1
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PREVENTION AVC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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University of Illinois at ChicagoRecruitingStroke, Ischemic | Stroke Hemorrhagic | Stroke, CerebrovascularUnited States
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Clinical Trials on Patients With Stroke
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Hospices Civils de LyonCompletedStroke | Transient Ischemic AttackFrance
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Military Institute od Medicine National Research...Active, not recruitingStroke | Healthy | Labyrinth Diseases | Cervical Spine Degenerative Disease | Visual Defects | Posterior Columns of the Spinal CordPoland
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Fondation Ophtalmologique Adolphe de RothschildNot yet recruiting
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University of the Philippines Manila - Philippine...CompletedStroke | Quality of Life | Stroke Rehabilitation | Stroke Rehabilitation and CaregiversPhilippines
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Fondazione Don Carlo Gnocchi OnlusScuola Superiore Sant'Anna di Pisa; Fondazione Policlinico Universitario Campus...Not yet recruitingStroke | Stroke Hemorrhagic | Upper Limb Rehabilitation | Stroke IschemicItaly
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Suleyman Demirel UniversityRecruiting
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Kırıkkale UniversityCompletedBalance; Distorted | Walking, Difficulty | Stroke SyndromeTurkey
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Istanbul Physical Medicine Rehabilitation Training...Completed
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Nantes University HospitalTerminatedEarly Mobilisation in Ischemic Stroke PatientsFrance
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Superior UniversityActive, not recruiting