Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:45 AM
Ignite Modification Date:
2025-12-25 @ 1:45 AM
NCT ID:
NCT04157894
Eligibility Criteria:
Inclusion Criteria:
* Passive data collection: All suspected malaria cases (fevers) that self-present to the national health system and are counted in the district health surveillance systems.
* Cross-sectional survey: Households in the district with a family member from the target age group.
* Residents of the household visited.
* Questionnaire: parent or guardian giving written informed consent (cross-sectional).
* Malaria screening: child aged 6 to 59 months from the above consenting household.
* Individuals of box sexes, not belonging to vulnerable categories (those with cognitive impairment or other person for whom full and open consent cannot be guaranteed) (Key informant interviews, focus group discussions, and participant observations).
* Individuals 20 years old and above (key informant interviews, focus group discussions, participant observations).
* Individuals of both sexes regardless of age (structured observations).
Exclusion Criteria:
* District non-residents.
* Malaria screening: history of recent (within one month) malaria infection or treatment with anti-malarial medication (cross-sectional).
* Parents or guardians who have not yet reached age of consent (20 years) and their children will not be included in study activities requiring consent.
* Individuals belonging to vulnerable categories (key informant interviews, focus group discussions, participant observations).
* Individuals unwilling and/or unable of giving consent (key informant interviews, focus group discussions, participant observations).
* Individuals below age of consent (20 years) (key informant interviews, focus group discussions, participant observations)
* Heads of households unwilling and/or unable of giving consent (structured observations)
* Individuals who do not wish to be included in observations will be excluded (structured observations)
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
6 Months
Study:
NCT04157894
Study Brief:
Protocol Section:
NCT04157894