- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT04570241
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
연구 개요
상세 설명
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.
연구 유형
등록 (예상)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Wilfred Fon Mbacham, PhD
- 전화번호: (+237) 677579180
- 이메일: wfmbacham@yahoo.com
연구 연락처 백업
- 이름: Rose Leke, PhD
- 전화번호: (+237) 699957329
- 이메일: roseleke@yahoo.com
연구 장소
-
-
Centre
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Yaoundé, Centre, 카메룬, +237
- 모병
- Mbandjock Health District
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연락하다:
- Fidelia Tarla, MSc
- 전화번호: (+237) 677577706
- 이메일: fideliatarla@gmail.com
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연락하다:
- Line Dongmo, MPH
- 전화번호: (+237) 675420201
- 이메일: dongmoline@gmail.com
-
-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
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.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 방지
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
---|---|
활성 비교기: 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
|
간섭 없음: 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. . |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
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
기간: 24 months
|
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
|
공동 작업자 및 조사자
수사관
- 연구 책임자: Esther Talla, MD, MC-CCAM
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (예상)
연구 완료 (예상)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
IPD 공유 기간
IPD 공유 액세스 기준
IPD 공유 지원 정보 유형
- CSR
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
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