Descriptive Study of Mental Activity (URGPSYMAY)
Descriptive Study of Mental Activity in the Emergency Department of the Centre Hospitalier de Mayotte
調査の概要
詳細な説明
This feature and the proximity of Mayotte with developing countries give this department different specificities, both culturally and medically. Indeed, the local population of lifestyle and specific beliefs, combining Islam and animism. Thus, a person with mental suffering is traditionally treated by a wizard who will come into contact with the spirits that inhabit the person, the community that supports the patient remains at home.
Mayotte is far behind compared to the metropolis where the supply of psychiatric care with a fragile population, a care network being created, and few downstream solutions To handle crisis situations, emergency unit and psychiatric liaison, speaking to general emergencies was established in 2010. It is currently the only access to emergency psychiatric care on the island.
The situations covered by this unit are for patients of all ages and all social and geographical origins, reflecting the demographics of the population.
Investigator has only quantitative data (number of patients / year) and has no qualitative analysis tool. No epidemiological research has been done to date in this direction.
The aim of our study was to analyze the impact of various psychiatric disorders represented Mayotte of the emergency hospital to get a statistical picture of its business.
This description will present to the scientific community the specifics of this department
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
-
-
Mamoudzou
-
Montpellier、Mamoudzou、フランス
- CH de MAYOTTE
-
-
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
説明
Inclusion Criteria:
Patient in need of psychiatric care in the emergency department
Exclusion Criteria:
- Patient leaves the emergency department against medical advice or fugue
- Patient leaves the service without the medical diagnosis is made
- Patient in exclusion period determined by a previous search
- Patients for whom it is impossible give clear information
- Patient who manifested their opposition to participate in research
- Patient minor whose parental agreement has been reached
- Patient on safeguarding justice whose guardian will not be contacted
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
- 主な目的：防止
- 割り当て：なし
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
他の：Psychiatry Consultation
Psychiatry Consultation, it is proposed by one of the investigators, patients that clinical data from this psychiatric examination, conducted as part of their usual care, are recorded as part of the research that their is proposed and explained.
An information note is then distributed and not collected their opposition
|
Psychiatry Consultation
|
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 |
|---|---|---|
|
Describe the mental activity
時間枠：1 day
|
Describe the mental activity of the emergency hospital of Mayotte (clinical observations obtained during routine psychiatric consultation) That is to say, describe the different psychiatric pathologies of all patients presenting to the emergency department of CH Mayotte.
|
1 day
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Estimated incidence rates of various psychiatric pathologies
時間枠：1 day
|
Estimated incidence rates of various psychiatric pathologies (clinical observations obtained during routine psychiatric consultation)
|
1 day
|
|
Search factors associated with different pathologies
時間枠：1 day
|
Search factors associated with different pathologies (clinical observations obtained during routine psychiatric consultation)
|
1 day
|
|
Creating a database for further research.
時間枠：1 day
|
Creating a database for further research (clinical observations obtained during routine psychiatric consultation)
|
1 day
|
協力者と研究者
捜査官
- 主任研究者：Nicolas MOLINARI、University hospital of Montpellier, Montpellier, France, 34295
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 (見積もり)
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。