Mobilization at the Level of Schools on the Behavioral Change in Favor of the Fight Against Malaria in Mbandjock
Evaluation of the Effect of Mobilization at School Level on Behaviour Change in Favor of Malaria Control in the Health District of Mbandjock in Cameroon
調査の概要
詳細な説明
General objective To determine the effect of awareness campaigns by school children targeting their communities on knowledge, attitudes and practices in malaria control in the Mbandjock health district.
Specific objectives
- To describe the socio-demographic characteristics of households in the health districts of Mbandjock and Sa'a at the time of the survey;
- To measure the change due the intervention on knowledge of malaria transmission, diagnosis, treatment and prevention in the health district of Mbandjock;
- To measure the change due the intervention on attitudes towards malaria diagnosis, treatment and prevention in the Mbandjock health district;
- To measure the change due the intervention on practices in the diagnosis, treatment and prevention of malaria in the Mbandjock health district.
Methodology Study design A two-arm, open label, randomized controlled clinical trial will be adopted with Mbandjock health district as the test district and Sa'a Health District a Control Health District.
Study site and study population The study population will be the entire population of the Mbandjock and Sa'a communities.
Sampling method The Lot Quality Assurance Sampling (LQAS) method was used. Since this method requires that the intervention zones be divided into supervision areas, the health areas of each district were considered as supervision areas. The health area was selected in the ratio 2:1. In the test district 11 health areas were used and 6 health district in the control district. 19 households were selected for each health area as required by the LQAS method.
Sample size A total of 209 pupils and 209 adults shall be enrolled from households in Mbandjock. Similarly, 114 pupils and 114 adults will be recruited in Sa'a. In addition, 57 teachers shall be enrolled in the District of Mbandjock only. A total of 703 participants shall be enrolled during the study.
Duration of study The study duration is three years. This will last from January 2017 to December 2020.
研究の種類
入学 (予想される)
段階
- 適用できない
連絡先と場所
研究場所
-
-
Centre
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Yaoundé、Centre、カメルーン、+237
- 募集
- Mbandjock Health District
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コンタクト：
- Fidelia Tarla, MSc
- 電話番号：(+237) 677577706
- メール：fideliatarla@gmail.com
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コンタクト：
- Line Dongmo, MPH
- 電話番号：(+237) 675420201
- メール：dongmoline@gmail.com
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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
説明
Inclusion Criteria:
- Children should be of school-going age.
- Children belong to an authorized school.
- Adult belonging to a household.
Exclusion Criteria:
- Children not going to school.
- Children not belonging to an authorized school.
- An adult that cannot be identified with any household.
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：ランダム化
- 介入モデル：並列代入
- 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 |
|---|---|
|
アクティブコンパレータ：Group A-Malaria toolkit
School children shall be trained on key malaria messages with a malaria toolkit.
From the training received, the pupils will carry out awareness-raising in communities with key messages learnt.
|
Knowledge, attitude, and practice on malaria
|
|
介入なし：Group B-No malaria toolkit
School children shall not be trained on key malaria messages with a malaria toolkit. Pupils will not carry out awareness-raising in communities with key messages. . |
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 |
|---|---|---|
|
Number of school children to be trained with the malaria toolkit in order to educate adults on malaria control in different communities in the Mbandjock Health District
時間枠：24 months
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The intervention group will include 209 children to be trained with a toolkit on malaria in order to educate 209 adults in their different communities
|
24 months
|
協力者と研究者
捜査官
- スタディディレクター：Esther Talla, MD、MC-CCAM
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
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
IPD 共有時間枠
IPD 共有アクセス基準
IPD 共有サポート情報タイプ
- CSR
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
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。