Prevalence of COVID-19 in a French Dependent Care Facility for the Elderly and in a French Long-term Care Unit: Observational Study (SPEED-COVID)
調査の概要
詳細な説明
Among people exposed to the COVID-19 (SARS-COV-2) pandemic, elderly people are considered as particularly vulnerable, especially those living in nursing homes or hospitalized. Furthermore, facilities / accommodations are registered among the main locations of COVID-19 clusters.
These observations have led the French government to establish specific protection measures and survey dependent care facilities for the elderly and long-term care units in the hospital.
With these new standards established, a long-term study of all the residents and geriatric inpatients of the care facilities attached to the Centre Hospitalier Sud Essonne (a general hospital located in Ile-de-France, France), can provide additional knowledge on COVID-19.
研究の種類
入学 (予想される)
連絡先と場所
研究連絡先
- 名前:Shidasp SIAMI, MD, PhD
- 電話番号:0033 1 60 80 79 40
- メール:ssiami@ch-sudessonne.fr
研究連絡先のバックアップ
- 名前:Delphine LEMAIRE-BRUNEL
- 電話番号:0033 1 60 80 79 88
- メール:dlemaire-brunel@ch-sudessonne.fr
研究場所
-
-
Essonne
-
Étampes、Essonne、フランス、91150
- 募集
- Centre Hospitalier Sud Essonne
-
コンタクト:
- Delphine LEMAIRE-BRUNEL
- 電話番号:0033 1 60 80 79 88
- メール:dlemaire-brunel@ch-sudessonne.fr
-
主任研究者:
- Shidasp SIAMI, MD, PhD
-
副調査官:
- Hafida BENHABIB
-
副調査官:
- Christine ANDREO
-
副調査官:
- El Hadi EL GHOUATI
-
副調査官:
- Laurence SAINSARD
-
副調査官:
- Christelle APARICIO
-
-
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:
- residents of the dependant care facility for the elderly
- inpatients of the long-term care unit
- from march, 2020 to december, 2021
Exclusion Criteria:
- opposition to participate in this 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
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 |
|---|---|---|
|
General prevalence of COVID-19
時間枠:Through the study completion, an average of 12 months
|
measures the prevalence of COVID-19 among the residents and geriatric inpatients, defined as resident and patients with positive serologic or RT-PCR test
|
Through the study completion, an average of 12 months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of asymptomatic residents/inpatients
時間枠:Through study completion, an average of 12 months
|
|
Through study completion, an average of 12 months
|
|
Number of symptomatic residents/inpatients
時間枠:Through study completion, an average of 12 months
|
Positive RT-PCR test or serologic test with symptoms
|
Through study completion, an average of 12 months
|
|
Number of residents/inpatients with severe form of COVID-19 which led to an hospitalization
時間枠:Through study completion, an average of 12 months
|
Positive RT-PCR test or serologic test and hospitalization
|
Through study completion, an average of 12 months
|
|
Number of residents/inpatients infected with COVID-19 and hospitalized in a critical care unit
時間枠:Through study completion, an average of 12 months
|
Positive RT-PCR test or serologic test and hospitalization in critical care unit
|
Through study completion, an average of 12 months
|
|
Number of residents/inpatients infected with COVID-19 and deceased
時間枠:Through study completion, an average of 12 months
|
Positive RT-PCR test or serologic test and deceased
|
Through study completion, an average of 12 months
|
|
Number of residents/inpatients vaccinated against COVID-19
時間枠:Through study completion, an average of 12 months
|
Positive RT-PCR test or serologic test and vaccinated with any authorized vaccine
|
Through study completion, an average of 12 months
|
|
Influencing factors of the prevalence of COVID-19 among residents/inpatients
時間枠:Through study completion, an average of 12 months
|
|
Through study completion, an average of 12 months
|
協力者と研究者
捜査官
- 主任研究者:Shidasp SIAMI, MD, PhD、Centre Hospitalier Sud Essonne
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (予想される)
研究の完了 (予想される)
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
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- SPEED-COVID19
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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