Perinatal DeathNCT07751432
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.
A study testing CC-ANC intervention group. in people with Perinatal Death and Hypertension, Pregnancy-Induced, run by University of Copenhagen at 1 site in Tanzania.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and older, women onlyHealthy volunteers can take part
- Conditions the study is for
- Perinatal Death, Hypertension, Pregnancy-Induced, Abortion, Spontaneous
- What is being tested?
- CC-ANC intervention group.
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,060 participants
- Where
- 1 siteTanzania
- Study dates
- 1 Mar 2026to 1 Dec 2028
- Phase
- Interventional
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- 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.
Who cannot join
- 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.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Tanzania1 site
21 Antenatal Care Clinics in Temeke District, Dar es Salaam.
Dar es Salaam, Temeke District
About this study
Official title: Pregnancy in the Context of Climate Change: Co-creating Climate-responsive Antenatal Care for Urban Tanzania (the CC-ANC Project).
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.
Read more
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.
Read the detailed description
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.
- Being tested
- CC-ANC intervention group.
- Keywords
- pregnancy, climate change, Antenatal care, Dar es Salaam, Tanzania, Co-creation, Trial, clinical guidelines, training
- Medical subject headings
- Perinatal Death, Hypertension, Pregnancy-Induced, Abortion, Spontaneous, Stillbirth
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
CC-ANC intervention group.Behavioural
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.
| Study group | Role | What they receive |
|---|---|---|
| The CC-ANC intervention. | Experimental | 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. Receives: Behavioral: CC-ANC intervention group. |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: From enrollment to live birth.
Secondary outcomes (2)
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.
Measured: 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.
Measured: Until 28 weeks gestational age.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Aug 2026
- Study start1 Mar 2026
- Primary completion1 Jul 2028 (estimated)
- Study completion1 Dec 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Perinatal DeathStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- This is a single-group, district-wide implementation study using a pre-post comparison design. The CC-ANC intervention will be co-created with and 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.
- Masking
- None (open label)
- Enrolment
- 1,060 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Copenhagen
- Sponsor type
- University, hospital or other
- Collaborators
- Aga Khan University
- Responsible party
- Principal investigator, Dan Meyrowitsch, University of Copenhagen
- Investigators
- Dan W Meyrowitsch, Professor, PhD, Principal investigator, University of Copenhagen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07751432
- Sponsor's protocol ID
- 23-11-KU
- Status last verified
- Aug 2026
- First submitted
- 3 Aug 2026
- Last updated
- 10 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- 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.
Publications
Maaloe N, Housseine N, Sorensen JB, Obel J, Sequeira DMello B, Kujabi ML, Osaki H, John TW, Khamis RS, Muniro ZSS, Nkungu DJ, Pinkowski Tersbol B, Konradsen F, Mookherji S, Mbekenga C, Meguid T, van Roosmalen J, Bygbjerg IC, van den Akker T, Jensen AK, Skovdal M, L Kidanto H, Wolf Meyrowitsch D. Scaling up context-tailored clinical guidelines and training to improve childbirth care in urban, low-resource maternity units in Tanzania: A protocol for a stepped-wedged cluster randomized trial with embedded qualitative and economic analyses (The PartoMa Scale-Up Study). Glob Health Action. 2022 Dec 31;15(1):2034135. doi: 10.1080/16549716.2022.2034135.
PubMed 35410590Maaloe N, Ortved AMR, Sorensen JB, Sequeira Dmello B, van den Akker T, Kujabi ML, Kidanto H, Meguid T, Bygbjerg IC, van Roosmalen J, Meyrowitsch DW, Housseine N. The injustice of unfit clinical practice guidelines in low-resource realities. Lancet Glob Health. 2021 Jun;9(6):e875-e879. doi: 10.1016/S2214-109X(21)00059-0. Epub 2021 Mar 23.
PubMed 33765437