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Enrolling by Invitation

NCT Number: NCT07751432

Pregnancy in the Context of Urbanicity and Climate Change. The Overall Aim of the Project is to Co-create, Implement, and Test New Clinical Guidelines in Order to Improve the Quality of Care in Antenatal Clinics in the Context of Urbanisation and Climate Change in Dar es Salaam, Tanzania.

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.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

21 Antenatal Care Clinics in Temeke District, Dar es Salaam.

Dar es Salaam, Temeke District, Tanzania

About this study

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 first work package is a situational analysis designed to characterize barriers and facilitators affecting the receipt and provision of ANC in this setting. This phase uses interdisciplinary mixed methods to examine structural conditions in ANC clinics, care processes across the antenatal and referral pathway, and the experiences of women and providers. Quantitative activities include facility assessments, mapping of current ANC guidance in use, structured exit interviews following ANC visits, and reviews of antenatal, gynecological, and birth-related records. The qualitative component includes participatory follow-up of women during pregnancy, documentation of care journeys inside and outside the health system, observations, in-depth interviews, and participatory approaches such as Photo Voice. These data are intended to inform both intervention design and interpretation of implementation effects.
  • The second work package focuses on co-creation of the intervention and its implementation strategy. Two synergistic versions of ANC guidance will be developed: one for pregnant women and their partners or families, and one for health providers. Both versions are expected to address routine pregnancy care, early-pregnancy complications, and complications later in pregnancy, while remaining adaptable to locally identified priorities. Co-creation will involve iterative engagement with women, providers, health-system leaders, and policymakers through repeated focus group discussions and other participatory activities. The research team will synthesize these inputs into guidance materials and associated training content, which will then undergo expert review. An embedded ethnographic component will examine how co-creators influence, experience, and shape the intervention development process.
  • 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.

  • A final work package will synthesize findings relevant to sustainability and scale-up. This phase will examine which contextual conditions and intervention features appear important for sustaining positive changes and for adapting the model to other urban settings. Particular attention will be paid to methodological lessons, delivery processes, and the implications of implementing a complex intervention in routine care environments. The protocol also indicates that recommendations for future research and practice, including a plan for subsequent cost-effectiveness assessment, will be developed if the intervention demonstrates promise.

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pregnant women attending antenatal care at participating government health facilities in Temeke District, Dar es Salaam, during the study period.
  • Able and willing to provide informed consent.

Exclusion criteria

  • Women not attending antenatal care at a participating government health facility in Temeke District.
  • Women who do not provide informed consent.
  • Individuals otherwise not eligible according to local ethical requirements.

Treatment and study plan

CC-ANC intervention group.

Behavioral

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.

Primary outcomes

  1. Rate of antepartum stillbirths (pre-hospital stillbirths).

    Time frame: From enrollment to live birth.

    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.

Secondary outcomes

  1. Preterm births.

    Time frame: At birth.

    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.

  2. Uncomplicated postabortion care.

    Time frame: Until 28 weeks gestational age.

    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.

Sponsors and collaborators

Lead sponsor

University of Copenhagen

Other

Collaborators

  • Aga Khan University

Registry information

Official study title

Pregnancy in the Context of Climate Change: Co-creating Climate-responsive Antenatal Care for Urban Tanzania (the CC-ANC Project).

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Aug 7, 2026
Registry last updated
Aug 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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