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Implementation of Multiple Micronutrient Supplementation (MMS) for Pregnant Women in Uganda

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 3 months later Sep 30, 2026 → Dec 31, 2026
See other at-risk trials from Johns Hopkins Bloomberg School of Public Health

Record History

See every version on ClinicalTrials.gov ↗

  1. Minor Primary completion pushed from Sep 30, 2026 to Dec 31, 2026
    • Eligibility criteria expanded, about 19 words
    • Secondary endpoints: details revised at 2 of 3 entries
    • Study description expanded, about 3 words
  2. Minor Primary completion date: Jun 30, 2026 to Sep 30, 2026v6
  3. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Jun 16, 2025 to Jun 18, 2025
    v5
  4. Notable Start date: May 15, 2025 to Jun 16, 2025v4
  5. Notable Start date: Apr 15, 2025 to May 15, 2025v3
  6. Minor Start date: Mar 17, 2025 to Apr 15, 2025v2
  7. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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 are to: * Describe the implementation of the MMS intervention (which consists of MMS product, a social behavior change communication (SBCC) strategy, capacity building, MMS supply chain support, monitoring, and evaluation) and explore acceptability, feasibility, fidelity, coverage, and potential for sustainability. * Determine the effect of dispensing MMS in different bottle counts on MMS adherence and ANC attendance among pregnant women. * Determine the cost and budget impact of MMS intervention implementation integrated in the Ugandan ANC service delivery system
Trial Details
NCT Number NCT06835738
Lead Sponsor Johns Hopkins Bloomberg School of Public Health
Collaborators: Vitamin Angels, UNICEF, Child and Family Foundation of Uganda, Kirk Humanitarian
Conditions
(from sponsor)
Nutrient Deficiency
Enrollment 4,077 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov