Implementation of Multiple Micronutrient Supplementation (MMS) for Pregnant Women in Uganda
Recruiting
N/A
Interventional Study
Nutrient Deficiency
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 0 – 80
- Sex
- Any
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 4,077 (estimated)
- Sponsor
- Johns Hopkins Bloomberg School of Public Health · Other
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About This Trial
The objective of this research is to understand how antenatal multiple micronutrient supplements (MMS) can be effectively implemented and scaled within the Uganda national health system context to support improved maternal nutrition and birth outcomes. Formative research has been conducted to design the implementation strategies that will be tested in this second phase of the study. The objectives…
Trial Locations
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Eligibility Criteria
Inclusion Criteria for Pregnant women- Enrolled for follow-up throughout pregnancy (sample 1)
* ≤24 weeks of amenorrhea/gestation as verified by health professionals
* Attending first ANC visit at government or PNFP health facilities.
* Accepted to take MMS at first ANC visit
Exclusion Criteria fo…
Contacts