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
調査の概要
研究の種類
入学 (実際)
連絡先と場所
研究場所
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Paris、フランス、75014
- Groupe Hospitalier Paris Saint-Joseph
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
説明
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
研究計画
研究はどのように設計されていますか？
デザインの詳細
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
|
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.
|
In addition to the usual care, the patient will have to complete a questionnaire analyzing the regularity of his follow-up by a physician.
|
この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Time until patient's care in the hospital after stroke's symptoms
時間枠：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.
|
Day 1
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Study the different effective means of primary prevention
時間枠：Day 1
|
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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協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。