An interventional study of CC-ANC intervention group. in Perinatal Death, Hypertension, Pregnancy-Induced and Abortion, Spontaneous, sponsored by University of Copenhagen. Enrolling by invitation at 1 site in Tanzania. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-10.
Sponsored by University of Copenhagen · Not applicable, Interventional, and Health services research
Tanzania's population is growing quickly, and Dar es Salaam is one of the fastest-growing cities in the world. At the same time, the city is increasingly affected by very hot weather, flooding, and air pollution. Many parts of Dar es Salaam do not have enough roads, drainage, housing, or public services for the number of people living there. About 70% of people live in unplanned neighborhoods, often in areas that are more exposed to flooding, heat, and pollution. This means many families face greater environmental risks in their daily lives.
The health system has also struggled to keep up with the city's rapid growth. Maternity services are often overcrowded, and many women and children in urban Tanzania now face worse birth outcomes than those in rural areas. Poverty, large gaps between rich and poor, weak infrastructure, and congested hospitals all make it harder for pregnant women to get the care they need.
This makes Dar es Salaam an important place to study how antenatal care can better respond to climate-related risks and the realities of urban life.
The study is expected to provide useful lessons not only for Tanzania, but also for other countries in sub-Saharan Africa and other low- and middle-income settings. This is especially important because more than half of the world's population now lives in cities, and most future urban growth is expected to happen in Africa and Asia.
The study will evaluate whether a co-created antenatal care program can improve the quality of pregnancy care and reduce serious pregnancy problems among pregnant women receiving care in government health facilities in Temeke District, Dar es Salaam, Tanzania. The program is designed for busy urban public clinics and includes guidance for pregnant women and their families, guidance for health providers, training for providers, a booklet for women, and text messages to support antenatal care visits and health information sharing. The study will be implemented in all 21 government facilities in the district that provide antenatal care and/or gynecological and childbirth care.
The study will use a pre-post implementation comparison design. Researchers will compare pregnancy care and outcomes before the program is introduced with pregnancy care and outcomes after implementation. The primary outcome is antepartum stillbirth, meaning a baby dies before labor starts. Secondary outcomes are preterm birth and the quality of uncomplicated postabortion care. The study will also examine whether the program improves the quality of antenatal care by helping health providers better identify and manage problems in pregnancy, especially high blood pressure disorders and early pregnancy complications such as miscarriage, and by improving women's understanding of key health information, the timing of the first antenatal visit, and the number of antenatal visits attended.
Information for the evaluation will be collected from antenatal cards, case files, hospital registers, medical records, interviews, and other study activities involving pregnant women and health providers. Researchers hope the findings will show whether a locally developed antenatal care improvement program can help prevent avoidable harm to mothers and babies and improve pregnancy care in a high-volume urban setting.
The PartoMa ANC study is a district-wide, mixed-methods implementation study designed to co-create, implement, and evaluate a context-tailored antenatal care (ANC) quality improvement intervention in Temeke District, Dar es Salaam, Tanzania. The study is grounded in the premise that pregnancy care in rapidly urbanizing, climate-vulnerable settings is shaped not only by clinical practice, but also by interacting social, environmental, and health-system constraints.
The intervention extends prior PartoMa work in childbirth care by shifting the focus upstream to ANC, with the aim of strengthening prevention, early detection, and initial management of pregnancy-related complications within routine public-sector services. The study is situated in the governmental health sector of Temeke District, which includes 21 facilities providing ANC, including facilties which also provide gynecological and childbirth care.
The scientific rationale for the study is that climate change, urbanization, and sexual and reproductive health and rights are closely interconnected, yet ANC models in low-resource urban settings rarely account for these interacting pressures. In Dar es Salaam, rapid population growth, unplanned settlement patterns, environmental hazards, and overstretched health services may contribute to poor pregnancy care experiences and adverse maternal and perinatal outcomes despite high contact with ANC services.
The protocol further builds on findings from the ongoing PartoMa studies suggesting persistent gaps in antenatal risk detection, birth preparedness, and management of untreated pregnancy complications. The present study therefore seeks to generate evidence on how a locally adapted ANC intervention can be embedded in routine care in a way that is feasible, acceptable, and responsive to the realities of a congested urban health system.
The intervention is informed by an explicit programme theory and by conceptual frameworks drawn from Complex Adaptive Systems and social practice theory. Within this framework, ANC is understood as a dynamic system in which women, families, providers, facilities, referral pathways, and wider contextual influences interact in non-linear ways. The study hypothesizes that intervention effects will arise through multiple linked mechanisms, including improved provider learning and decision-making, improved uptake and integration of ANC guidance into existing practice, and greater alignment between care content and the needs, preferences, and lived realities of pregnant women. This theory-driven approach is intended not only to assess whether the intervention works, but also to understand how and under what contextual conditions it may be implementable and scalable.
The study is organized into four interlinked work packages
The implementation phase will introduce the intervention across all eligible government facilities in Temeke District using a pre-post comparison design. Planned implementation strategies include training selected facilitators who, together with the research team, will support recurring training sessions for healthcare providers, drawing on or integrating with the existing PartoMa training structure. Women attending ANC will receive a booklet version of the guidance, and an mHealth component will supplement in-person care through health- and visit-related text messaging. Because the intervention is delivered at district scale and within routine services, the study is designed to evaluate effectiveness under real-world conditions rather than under tightly controlled experimental conditions.
Evaluation is structured along the proposed causal pathway from intervention exposure to provider learning, service delivery processes, and pregnancy-related endpoints recorded elsewhere in the study record. Pre-intervention measurements generated during the situational analysis will serve as the main baseline, supplemented by an additional baseline period immediately preceding implementation for routinely collected pregnancy outcome data. Post-implementation assessment will draw on multiple complementary data sources, including criterion-based audits of antenatal cards and case files, hospital registers, medical records, structured interviews, and other participant-level and facility-level documentation collected by trained research assistants. Quantitative analyses are planned primarily as comparisons of pre- and post-implementation measures, with stratified and adjusted analyses undertaken when relevant. Qualitative analyses will be used to interpret implementation processes, user experiences, contextual influences, and mechanisms of change.
The study will be conducted in accordance with the Declaration of Helsinki, with ethics approvals sought in Tanzania and informed consent obtained from women and health providers participating in primary data collection activities.
120 studies on the registry are indexed under Perinatal Death; 25 are open to participants now.
This study's planned enrollment of 1,060 is above the median of 427 across 84 interventional studies indexed under Perinatal Death.
Browse Perinatal Death studies →University of Copenhagen is the lead sponsor of 466 studies on the registry; 64 are open to participants now.
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Exclusion Criteria:
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You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
This is a single-group, district-wide implementation study using a pre-post comparison design. After the baseline data collection, the CC-ANC intervention will be introduced in all 21 government health facilities in Temeke District that provide antenatal care and/or gynecological and childbirth care. There is no concurrent control group and no randomized assignment to different interventions. Study effects will be evaluated by comparing key process and clinical indicators measured before implementation with the same indicators measured after implementation under routine service conditions.
Behavioral: CC-ANC intervention group.
The intervention includes two co-created sets of ANC guidance, one for pregnant women and their partners/families and one for health providers, covering routine pregnancy care, first-trimester complications, and second- and third-trimester complications. Implementation includes training of selected facilitators and recurring provider training sessions, distribution of women's booklet versions of the guidance during ANC visits, and possibly an mHealth component providing health- and visit-related text messages to support and complement in-person ANC services.
Rate of antepartum stillbirths (pre-hospital stillbirths).
Antepartum stillbirths are the study's primary outcome indicator. The outcome will be assessed as the rate of pre-hospital stillbirths and compared between the pre-intervention and post-intervention periods to evaluate whether the CC-ANC intervention reduces adverse pregnancy outcomes. The protocol explicitly identifies antepartum stillbirths as the primary indicator and later operationalizes this outcome as pre-hospital stillbirths for sample size estimation and analysis.
Time frame: From enrollment to live birth.
Preterm births.
This outcome will be assessed using pregnancy outcome data collected through the PartoMa data collection system extended to all eight birthing facilities in Temeke District, and compared between the pre-intervention and post-intervention periods to evaluate whether the intervention reduces adverse pregnancy outcomes.
Time frame: At birth.
Uncomplicated postabortion care.
This measure will be assessed through case file reviews and criterion-based audits in gynecological wards, focused on care for first-trimester complications including miscarriages and unsafe abortions, and compared between the pre-intervention and post-intervention periods.
Time frame: Until 28 weeks gestational age.
Plan to share: No — Individual participant data will not be shared because external sharing of de-identified participant-level data was not included in the informed-consent process or the original ethical approval framework. The study collects sensitive maternal, reproductive and clinical information from a geographically defined population attending specific health facilities in Temeke District, Dar es Salaam. Even after removal of direct identifiers, combinations of clinical, demographic, facility and geographical variables may create a risk of deductive re-identification. In addition, secondary use and transfer of the data are subject to Tanzanian ethical approvals, applicable data-protection requirements, institutional governance procedures and agreements with participating facilities and partner institutions.
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