Health promotion and provision of RMNCH services
BehavioralImplementation of quality, high-impact interventions at institutional and community levels to increase access to and utilization of RMNCH services
NCT Number: NCT03774602
This study evaluates changes in knowledge, attitudes, practices and coverage of key reproductive, maternal, newborn, and child health (RMNCH) areas, including malaria, family planning (FP), nutrition, water, sanitation and hygiene (WASH), and gender equity among the population in Nampula and Sofala provinces targeted by the Maternal and Child Survival Program (MCSP) in Mozambique.
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Notify Me15 year–49 year
All sexes
Interventional
Not applicable
Angoche District, Community Setting, Angoche, Nampula, Mozambique
The specific objectives of the study are to:
This study is a final program evaluation that will use a mixed methods approach, including both quantitative and qualitative data collection.
Quantitative data will be collected through a cross-sectional KAPC household survey of mothers and fathers of children age 0-23 months, replicating the same KAPC questionnaire that was conducted at baseline in 2016 in the same geographic areas. Questions were harmonized with the DHS and MICS where appropriate. Findings from the endline KAPC survey will be compared to findings from the baseline survey to assess changes over time in the primary outcomes of interest.
Qualitative data will be collected through focus group discussions (FGDs) and in-depth interviews (IDIs) with clients (mothers and fathers of children age 0-23 months) and health providers in MCSP-supported areas. The qualitative component will be conducted to help us gain a more in-depth understanding of the influence of male engagement interventions on couples' decision-making and care-seeking related to RMNCH as well as the barriers and facilitators that affected the experience of identified women who were referred to health facilities for obstetric or newborn complications. We will explore both client and provider experiences with gender-equitable male engagement practices, as well as individual client referral narratives related to obstetric or newborn complications.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
(KAPC survey):
Exclusion criteria
(KAPC survey): Women 15-17 years without parent permission to participate in study
Inclusion criteria
(Referral narrative interviews): Women who: a) delivered in the last 12 months who experienced obstetric complications; b) whose newborn experienced complications in the last year; c) whose child 0-59 months experienced an illness in the last year
Inclusion criteria
(Provider interviews):
Exclusion criteria
(Provider interviews): Has been working in the facility for < 6 months
Inclusion criteria
(Male engagement FGDs):
Implementation of quality, high-impact interventions at institutional and community levels to increase access to and utilization of RMNCH services
Time frame: 2 years
Percentage of last-born children age 0-23 months who were born in a health facility
Time frame: 2 years
Percentage of mothers of children age 0-23 months who had four or more antenatal care visits while pregnant with their youngest child
Time frame: 2 years
Percentage of children age 12-23 months who received a Penta 1 vaccination but did not receive a Penta 3 vaccination according to or card verified at the time of the survey
Time frame: 2 years
Percentage of mothers of children age 0-23 months who made birth preparations before the birth of their youngest child
Time frame: 2 years
Percentage of women of reproductive age who have discussed with her partner whether to use a FP method
Time frame: 2 years
Percentage of infants 0-5 months of age who are fed exclusively with breast milk
Jhpiego
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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