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Maternal and Child Health clinical trials

View clinical trials related to Maternal and Child Health.

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NCT ID: NCT06354621 Completed - Clinical trials for Maternal and Child Health

Impact of Vitamin D Supplementation on Fetomaternal Outcomes in LTBI Pregnant Females

RCT
Start date: September 1, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of this randomized controlled trial is to see the effect of vitamin D supplementation on fetomaternal outcomes in pregnant females with Latent Tuberculosis infection The main question[s] it aims to answer are: If Vitamin D supplementation has any impact on maternal outcomes. If Vitamin D supplementation has any impact on fetal outcomes.

NCT ID: NCT04278612 Completed - Clinical trials for Maternal and Child Health

Evaluation of the Effectiveness of a Quality Improvement Intervention

Start date: January 18, 2016
Phase: N/A
Study type: Interventional

This rigorous evaluation demonstrated that implementation of a time-limited quality improvement strategy effectively improved coverage of some components of an integrated maternal and child health service in a complex health environment, but we were unable to achieve the changes needed to provide a comprehensive package of care for mothers and children.

NCT ID: NCT02979418 Completed - HIV Clinical Trials

Pii Ngima: Consequences of Water Insecurity for Maternal and Child Health

PEN
Start date: February 2016
Phase:
Study type: Observational

This study will implement the validated household-level water insecurity scale developed by study investigators among a cohort of postpartum women in Nyanza, Kenya and will assess a range of outcomes linked to water insecurity, such as viral load, hydration status, maternal depression, stress, food insecurity, and cognitive development.

NCT ID: NCT02974972 Completed - HIV Clinical Trials

Pith Moromo 2: Cohort to Study Health Consequences of Food and Nutrition Insecurity During Pregnancy and Lactation

PM2
Start date: August 2014
Phase:
Study type: Observational

In this study, the investigators conducted research among HIV-infected and -uninfected pregnant and lactating women to understand the potential role and importance of food insecurity on participant physical and psychosocial health and nutrition.

NCT ID: NCT02925429 Completed - HIV Clinical Trials

PostNAPS: FI, Nutrition, and Psychosocial Health Among Women of Mixed HIV Status and Their Infants in Gulu, Uganda

PostNAPS
Start date: May 2013
Phase:
Study type: Observational

PostNAPs was a continuation of the PreNAPs study. 246 women were enrolled in the postnatal period with the primary scientific objective of determining whether food insecurity was an independent risk factor for poor maternal nutritional or psychosocial outcomes or for sub-optimal infant feeding practices.

NCT ID: NCT02046018 Completed - Clinical trials for Maternal and Child Health

Integrated Community Case Management (ICCM) Delivered by Village Health Teams in Bushenyi District in Uganda

Start date: October 2009
Phase: N/A
Study type: Interventional

In Sub-Saharan Africa (SSA), many children die from diarrhoea, acute respiratory illness (ARI) and malaria, despite well- recognized, inexpensive and highly effective treatments, since health access and human resources are limited. Healthy Child Uganda (HCU) is a Ugandan-Canadian partnership that since 2003, has developed, implemented and evaluated a Village Health Volunteer (VHV) program in 175 rural villages. Volunteers, selected by peers, provide health education and refer sick children. Volunteer retention (94%) and significant decreases in child deaths are remarkable. Now, HCU wonders whether VHV scope can extend to provide treatment for sick children using Oral Rehydration Salts (ORS)/Zinc, antibiotics, and antimalarials. Use of lay providers in this capacity, called integrated community case management (iCCM), has been proposed as a potential inexpensive solution to SSA's human health resource crisis. PRIMARY QUESTION: In rural southwest Uganda, can iCCM provided by lay volunteers, improve the proportion of children with diarrhoea receiving ORS/Zn, ARI receiving antibiotics, and fever/malaria receiving antimalarials? Secondary study questions consider VHV capacity to prescribe appropriate drug, dose, duration; iCCM acceptance by family, and VHV; VHV retention/motivation; program cost. Selected VHV will be iCCM trained then receive treatments for distribution. Qualitative and quantitative methods including household surveys, and focus groups will consider pre/post intervention differences and differences in control and intervention populations. A research short course and micro research grants (~ $3000 to multidisciplinary groups pursuing relevant questions) will promote health system evaluation capacity. Lessons learned are critical as SSA countries move forward in planning for increased iCCM programming.