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 @ 12:43 AM
Ignite Modification Date:
2025-12-25 @ 12:43 AM
NCT ID:
NCT06613867
Eligibility Criteria:
Inclusion Criteria for the main study (quasi-experimental study with a before-after approach)
* Aggregated data of pregnant women, regardless of the age of their pregnancy, and
* attending the health facilities included in the study
Inclusion Criteria for participating in the observational cohort:
* Being a pregnant woman residing in the study area and
* attending the health facilities included in the study and
* with a given individual consent.
Inclusion Criteria for participating in the sub-study on intervention's acceptability and feasibility:
* traditional birth attendants (TBAs) or
* health workers working in health facilities or
* community health workers or
* community representatives or
* women who have already given birth or pregnant women or their husbands AND
* All with a given individual consent AND
* All being part of the study area.
Healthy Volunteers:
True
Sex:
ALL
Study:
NCT06613867
Study Brief:
Protocol Section:
NCT06613867