MidwiferyNCT05237375
MIDWIZE - Strengthening Midwives
An observational study of Midwifery, run by Karolinska Institutet at 4 sites in Uganda.
Trial summary
This PhD project aims to explore how midwives can take the lead in implementing and enhancing evidence-based quality improvement (QI) components within maternal and newborn health care in Uganda. Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Midwifery
- What is being tested?
- The MIDWIZE model
- How many people
- 1,000 participants
- Where
- 4 sitesUganda
- Study dates
- 10 Mar 2022to 1 Sep 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
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 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Pregnant women coming to give birth at Naguru Hospital during or after the implementation of the MIDWIZE model.
Who may be able to join
- People above the age of 18 with uncomplicated singleton full-term pregnancies and births (i.e. between weeks 37 + 0 - 42 + 0).
Who cannot join
- People under the age of 18, people with complications in pregnancy or with a planned c-section.
Trial locations and contacts
4 sites in 1 country.
Uganda4 sites, 3 recruiting
- Completed
CUFH Naguru
Kampala, Naguru
- Recruiting
Kawalla Hospital
Kampala
Sr Judith, RM, +256 706 298230
- Recruiting
Kawempe Hospital
Kampala
Sylvia Kalegere, RM, +256773169422
- Recruiting
Kisenye Hospital
Kampala
Lydia Were, +256772951008
About this study
Official title: MIDWIZE - Strengthening Midwives to Implement and Sustain Quality Improvements to Optimise Maternity Care: A Longitudinal Observational Study in Uganda
This PhD project aims to explore how midwives can take the lead in implementing and enhancing evidence-based quality improvement (QI) components within maternal and newborn health care in Uganda.
The MIDWIZE conceptual framework will be used to understand the complexity of sustainably enhancing maternal and newborn healthcare. The project will start with a multisectoral co-creation process and subsequently involve online and onsite capacity building for midwives on selected evidence-based practices and implementation strategies. The project applies a mixed-method research approach, including focus groups discussions, interviews, quantitative data on health outcomes and a tool evaluating midwives' sense of power and autonomy.
Read the detailed description
Traditionally, Quality Improvement (QI) initiatives in healthcare have often centered on the implementer's viewpoint, neglecting the active involvement of staff in shaping or leading interventions, or viewing them merely as passive objects resistant to change. Previous research in QI and organizational development indicates that when individuals or teams identify and take ownership of problems, the resulting actions are more effective and sustainable, as opposed to when solutions are imposed externally. Thus, our hypothesis was that by empowering midwives to spearhead change initiatives, involving them in the co-creation of interventions to ensure relevance and ownership, and equipping them with QI leadership and practical skills, midwives would effectively enhance healthcare service quality, foster the adoption of evidence-based practices, and ultimately improve health outcomes for women and newborns.
MIDWIZE is a model based on multisectoral collaboration to enhance evidence-based practices through Midwife-Led Care (MLC) and interdisciplinary teamwork.
Focusing on midwives as the primary health care providers at all levels of a country's maternal and reproductive health care system is an elementary part of the MIDWIZE model. Utilising midwives' potential through MLC facilitates relational, safe, cost-effective, and patient-centred care.
When additional support is required, the MLC needs to be provided in an environment that successfully takes advantage of different clinical professions' competencies. Working towards shared goals and having a clear understanding of each team member's responsibilities in an interdisciplinary team are central factors for utilising human and financial resources.
At the heart of the MIDWIZE model is enhancing the use of evidence-based practices and international guidelines for maternal and newborn health care - focusing on a healthy mother, a healthy child, a positive birth experience, and respectful care. The Z in MIDWIZE stands for the importance of "Zero separation" between the mother/birthing parent/caregiver and newborn in the early postpartum period - an evidence-based practice enhancing neonatal health outcomes, breastfeeding, and the bonding between mother/birthing parent/caregiver and child.
A prerequisite to sustainably implement or enhance these elements in a country's health system is to establish multisectoral collaborations between the four sectors (i) education, (ii) regulation, (iii) associations, and (iv) civil society. Also, the broader health system and its decision- and policymakers' readiness must be considered to create a sustainable system with continuous quality improvements within the education, regulation, and associations sectors.
General objective - this PhD project aims to explore how midwives can co-create and lead QI within midwifery and how this impacts the uptake of evidence-based practises and health outcomes for women and newborns.
Sub-study 1 - Co-creating and developing the intervention and the implementation Rationale: The involvement of stakeholders in the development of complex interventions is essential to ensure that the intervention and process are relevant, acceptable, and user friendly.
Specific objective: Describe the co-creation process and explore the needs and determinants of a midwife-led quality improvement targeting evidence-based midwifery practices.
Research Question: How do multisectoral stakeholders describe ways to implement the MIDWIZE model, how can the model be adapted to the local context and what strategies for implementation should be taken? (As the remaining parts of the intervention will be co-created, the following parts are preliminary)
Sub-study 2 - Implementation and evaluating the sustainability of the implementation Rationale: This study will explore how midwives can take the lead in implementing or enhancing evidence-based practical components of maternal care. Long-term sustainability is vital in order to maximise the potential benefits of implementation. Therefore, this study will, apart from measuring the midwives' QI projects' during the implementation phase, also measure the long-term impact six months after the project has ended. Based on the co-creation, the Midwize intervention targets three evidence-based practices where a gap between evidence and practice existed: dynamic birth positioning, empowering women in decision-making about birth positions, perineal protection, and intrapartum support. Spearheaded by a team of midwives known as the "Midwize Ambassadors," this seven-month quality improvement initiative was co-developed with expert guidance in quality enhancement and practical midwifery skills. Employing Plan-Do-Study-Act (PDSA) cycles aligned with the Model for Improvement framework, the intervention adopted a train-the-trainer methodology and conducted weekly online support sessions.
Aim: To investigate the process of a midwife-led QI intervention and the uptake of evidence-based midwifery practises.
Sub-study 3 - Outcomes Aim: To investigate the outcomes of a midwife-led QI intervention targeting evidence-based midwifery practises.
Sub-study 3 - Scaling up Aim: To explore how the Midwize intervention can be scaled up at other facilities in Kampala and what the health outcomes are for women and newborns.
Methodology Study Site Naguru maternity unit in Kampala, Uganda, is a public facility with 9000 births/year.
Study design and data collection The overall study design is a longitudinal observational study. Sub-Study 1
Focus Group Discussions (FGD) and workshops will be held in three steps:
- Clinical staff (e.g., midwives, nurses, obstetricians, and assistant nurses), stakeholders at professional associations, academia (e.g., midwife educators, researchers, and students), and decision-makers (e.g., staff at ministry of health and hospital managers) will be included (n=36, divided into six groups). Barriers and facilitators for multisectoral collaboration will be highlighted during the workshops.
- Members of the civil society (e.g., the projects main stakeholder - the childbearing women and their relatives) will be included in order to deliver an adequate and acceptable intervention (n=36, divided into six groups).
- Clinical staff and managers will be included to investigate the practical implementation aspects of the project and the birth unit's adherence to national policies and clinical guidelines (n=21, divided into three groups).
Sub-Study 2 Quantitative data will be collected during and after implementing the quality improvement components. The post-measurement data will be collected on the chosen components three and six months after project implementation to measure if the midwife-led quality improvement project has been sustained.
Data is collected through observations during birth and interviews with women.
Sub-study 3: Same data will be used as for Sub-study 2 Sub-study 4: Same as in sub-study 2 but at two new intervention sites and one control site.
Sample size Sub-Study 1 Part 1 - n=36 (Clinical staff, professional associations, academia, decision-makers) Part 2 - n=36 (childbearing women and their relatives) Part 3 - n=21 (clinical staff and managers) Sub-Study 2 and 3 As this is a quality improvement project, the number of participants depends on when the targeted goal is accomplished and the total number of participants can therefore not be decided on beforehand. The targeted goal for the specific unit will be decided in dialogue with staff and management.
However, a preliminary calculation with an estimated increase of the components by 25% would suggest a minimum of 266 women during the intervention and 266 women six months after the intervention to measure the long term sustainability.
Based on previous studies, the prevalence of the three components in connection with childbirth amounts to 50%. The size of the study population is based on a calculation with 80% strength and a 95% confidence interval. A clinically significant increase in the number of women giving birth with the three components of the intervention and who are satisfied with their delivery is estimated at 25%, i.e. from 50% of women to 75% of women. To achieve this level of strength, a study population of 242 women is required. With an estimated dropout rate of 10%, there will be a study population of 266 women. To study the project's long-term sustainability, a repeated measurement that includes 266 women six months after completing data collection 2 will be done.
Measurement during the implementation phase - n=266 (birthing women) Post measurement - n=266 (birthing women)
Sampling procedure Sub-Study 1 Part 1 - A targeted selection process will be applied, and people will be included based on experience, knowledge and position in the care system (i.e. decision-makers at different levels).
Part 2 - A random sampling will be made with stakeholders of the community (in this case, pregnant women or women who recently gave birth at the clinic) Part 3 - A targeted sampling with clinical staff and managers based on profession and experience
Sub-Study 2, 3 and 4 will include all women above the age of 18 with uncomplicated full-term pregnancies and births (i.e. between weeks 37 + 0 - 42 + 0).
Pre-testing No Pre-testing will be performed as this is a quality improvement project. The data collection for sub-study two will start when the implementation starts. The outcomes will be followed until sufficient data has been achieved.
Field editing of data The research midwife will fill in the data for sub-study 2, 3 and 4 in a data collection protocol, which will be entered electronically.
Missing data. The research midwife of the day will fill in any missing data in dialogue with the clinical staff. Missing data will be continuously monitored as the data sampling will be reported online (via a secured 2-step verification platform approved to share research data).
Data Management Computer packages to use. SPSS Quality control In the qualitative parts of the project, the trustworthiness of the data will be ensured by recording interviews and FGD, transcribing verbatim, triangulation by including other researchers in the team in the analysis, regular discussions on the analysis to reach a common understanding within the team.
The quantitative data quality will be checked by random control samples made by members of the research group. A statistician will be consulted during the analysis and an electronic logbook will be kept in order for external researchers to check the procedure.
Data Analysis Presentation of data The findings will be published in peer-reviewed academic journals.
Analysis Techniques Sub-Study 1 - Thematic analysis, according to Braun \& Clark (2006) Sub-Study 2, 3 and 4 - SPSS will be used for descriptive and comparative analysis of the data
- Conditions
- Midwifery
- Being tested
- The MIDWIZE model
- Keywords
- Midwifery, Midwife Led Care, MIDWIZE
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
The MIDWIZE modelOther
So-called "MIDWIZE ambassadors" are planned to be appointed to lead the clinical implementation of the quality improvement components.
Initial training workshops will be held with the ambassadors on practical aspects of the chosen components and how to explain their benefits to the units' staff. Training will also be provided on how to enhance interdisciplinary teamwork and coordinate quality improvements. The workshops will be held onsite at Naguru hospital and online via the project's "MIDWIZE virtual platform". The ambassadors will themselves hold training workshops to support midwives and other healthcare providers at the clinics during the implementation of the quality improvements components. The virtual MIDWIZE platform will contain videos, posters, presentations, and other training material that the ambassadors can utilise to enhance the units' capacity and engage their colleagues.
| Study group | Role | What they receive |
|---|---|---|
| The MIDWIZE model | Pregnant women giving birth during at Naguru maternity ward during the intervention period
It's only Sub/study 2 in this PhD project which is a clinical trial and which is described onwards.
Sub-study 2 will include all women above the age of 18 with uncomplicated full-term pregnancies and births (i.e. between weeks 37 + 0 - 42 + 0) giving birth at the delivery ward during the implementation phase.
Data will be collected during the implementation of the quality improvement components. Receives: Other: The MIDWIZE model | |
| The MIDWIZE model - postintervention | Pregnant women giving birth at Naguru maternity ward 3 and 6 months post intervention period. Sub-study 2 will include all women above the age of 18 with uncomplicated full-term pregnancies and births (i.e. between weeks 37 + 0 - 42 + 0) giving birth at the delivery ward 3 and 6 months after the implementation phase. Data will be collected after implementing the quality improvement components. The post-measurement data will be collected on the chosen components six months after project implementation to measure if the midwife-led quality improvement project has been sustained. | |
| The MIDWIZE model - scaling up | The intervention will be scaled up at three additional sites and will include all women above the age of 18 with uncomplicated full-term pregnancies and births (i.e., between weeks 37 + 0 - 42 + 0) giving birth at the delivery ward during the implementation phase. |
What is being measured
The primary outcome is the main question the study is designed to answer.
The uptake of the midwives quality improvments
Three evidence based midiwfery practises (i) dynamic birth positions, (ii) intrapartum support and (iii) prevetion of perineal tears .
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Apgar score
Apgar score. The Apgar score is a rapid assessment of a newborn's health, conducted one minute and five minutes after birth, evaluating their heart rate, respiratory effort, muscle tone, reflex irritability, and color. Each component is scored from 0 to 2 points, with a maximum score of 10 points.
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Perineal tear
Perineal tear (divided in unsutured tear, sutured tear, sphinkter tear)
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Episiotomy
Was episiotomy performed at birth
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Postpartum haemorrhage
Postpartum haemorrhage
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Neonatal and maternal deaths
Neonatal and maternal deaths
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Secondary outcomes (12)
Mothers age
Mothers age
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Level of education
Level of education for mothers giving birth during the intervention.
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Marital status
Marital status
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Area of living
Area of living
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Employment
Employment
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Obstetric background
Obstetric background
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.6months after implementation phase is completed.
Gestation week
Gestation week
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Mode of delivery
Mode of delivery
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Length of second stage of labour
Length of second stage of labour
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Birth weight
Birth weight
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Transfer to a neonatal unit
Transfer to a neonatal unit
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Skin-to-skin care
the number of minutes of skin-to-skin observed and documented by a Research Assisatant. Maximum observation time is 1hour.
Measured: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Feb 2022
- Study start10 Mar 2022
- Primary completion1 May 2024 (estimated)
- Study completion1 Sep 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (5)Papers the sponsor has linked to this study.
- Other trials for MidwiferyStudies of the same condition, open and under way.
- More trials run by Karolinska InstitutetThe sponsor's other registered studies.
- 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
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 1,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Karolinska Institutet
- Sponsor type
- University, hospital or other
- Collaborators
- The Swedish Institute
- Responsible party
- Principal investigator, Helena Lindgren, Karolinska Institutet
- Investigators
- Helena Lindgren, PhD, Principal investigator, Karolinska Institutet
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05237375
- Sponsor's protocol ID
- MIDWIZE
- Status last verified
- Apr 2024
- First submitted
- 7 Dec 2021
- Last updated
- 29 Apr 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Berta M, Lindgren H, Christensson K, Mekonnen S, Adefris M. Effect of maternal birth positions on duration of second stage of labor: systematic review and meta-analysis. BMC Pregnancy Childbirth. 2019 Dec 4;19(1):466. doi: 10.1186/s12884-019-2620-0.
PubMed 31801479Hailemeskel S, Alemu K, Christensson K, Tesfahun E, Lindgren H. Health care providers' perceptions and experiences related to Midwife-led continuity of care-A qualitative study. PLoS One. 2021 Oct 14;16(10):e0258248. doi: 10.1371/journal.pone.0258248. eCollection 2021.
PubMed 34648571Nove A, Friberg IK, de Bernis L, McConville F, Moran AC, Najjemba M, Ten Hoope-Bender P, Tracy S, Homer CSE. Potential impact of midwives in preventing and reducing maternal and neonatal mortality and stillbirths: a Lives Saved Tool modelling study. Lancet Glob Health. 2021 Jan;9(1):e24-e32. doi: 10.1016/S2214-109X(20)30397-1. Epub 2020 Dec 1.
PubMed 33275948Blomgren J, Wells MB, Erlandsson K, Amongin D, Kabiri L, Lindgren H. Putting co-creation into practice: lessons learned from developing a midwife-led quality improvement intervention. Glob Health Action. 2023 Dec 31;16(1):2275866. doi: 10.1080/16549716.2023.2275866. Epub 2023 Nov 6.
PubMed 37930253Blomgren J, Wells MB, Amongin D, Erlandsson K, Wanyama J, Afrifa DA, Lindgren H. Improving apgar scores and reducing perineal injuries through midwife-led quality improvements: an observational study in Uganda. BMC Public Health. 2025 Jan 3;25(1):19. doi: 10.1186/s12889-024-21137-w.
PubMed 39754106
Study at a glance
From the registry record, last updated by the sponsor on 29 Apr 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- MIDWIZE - Strengthening Midwives to Implement and Sustain Quality Improvements to Optimise Maternity Care: A Longitudinal Observational Study in Uganda
- ClinicalTrials.gov ID
- NCT05237375
- Acronym / sponsor ID
- MIDWIZE
- Conditions
- Midwifery
- Keywords
- Midwifery, Midwife Led Care, MIDWIZE
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 1,000 participants (estimated)
- Lead sponsor
- Karolinska InstitutetUniversity, hospital or other
- Collaborators
- The Swedish Institute
- Study start
- 10 Mar 2022 (actual)
- Primary completion
- 1 May 2024 (estimated)
- Study completion
- 1 Sep 2025 (estimated)
- First posted
- 14 Feb 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This PhD project aims to explore how midwives can take the lead in implementing and enhancing evidence-based quality improvement (QI) components within maternal and newborn health care in Uganda.
The MIDWIZE conceptual framework will be used to understand the complexity of sustainably enhancing maternal and newborn healthcare. The project will start with a multisectoral co-creation process and subsequently involve online and onsite capacity building for midwives on selected evidence-based practices and implementation strategies. The project applies a mixed-method research approach, including focus groups discussions, interviews, quantitative data on health outcomes and a tool evaluating midwives' sense of power and autonomy.
Detailed description
Traditionally, Quality Improvement (QI) initiatives in healthcare have often centered on the implementer's viewpoint, neglecting the active involvement of staff in shaping or leading interventions, or viewing them merely as passive objects resistant to change. Previous research in QI and organizational development indicates that when individuals or teams identify and take ownership of problems, the resulting actions are more effective and sustainable, as opposed to when solutions are imposed externally. Thus, our hypothesis was that by empowering midwives to spearhead change initiatives, involving them in the co-creation of interventions to ensure relevance and ownership, and equipping them with QI leadership and practical skills, midwives would effectively enhance healthcare service quality, foster the adoption of evidence-based practices, and ultimately improve health outcomes for women and newborns.
MIDWIZE is a model based on multisectoral collaboration to enhance evidence-based practices through Midwife-Led Care (MLC) and interdisciplinary teamwork.
Focusing on midwives as the primary health care providers at all levels of a country's maternal and reproductive health care system is an elementary part of the MIDWIZE model. Utilising midwives' potential through MLC facilitates relational, safe, cost-effective, and patient-centred care.
When additional support is required, the MLC needs to be provided in an environment that successfully takes advantage of different clinical professions' competencies. Working towards shared goals and having a clear understanding of each team member's responsibilities in an interdisciplinary team are central factors for utilising human and financial resources.
At the heart of the MIDWIZE model is enhancing the use of evidence-based practices and international guidelines for maternal and newborn health care - focusing on a healthy mother, a healthy child, a positive birth experience, and respectful care. The Z in MIDWIZE stands for the importance of "Zero separation" between the mother/birthing parent/caregiver and newborn in the early postpartum period - an evidence-based practice enhancing neonatal health outcomes, breastfeeding, and the bonding between mother/birthing parent/caregiver and child.
A prerequisite to sustainably implement or enhance these elements in a country's health system is to establish multisectoral collaborations between the four sectors (i) education, (ii) regulation, (iii) associations, and (iv) civil society. Also, the broader health system and its decision- and policymakers' readiness must be considered to create a sustainable system with continuous quality improvements within the education, regulation, and associations sectors.
General objective - this PhD project aims to explore how midwives can co-create and lead QI within midwifery and how this impacts the uptake of evidence-based practises and health outcomes for women and newborns.
Sub-study 1 - Co-creating and developing the intervention and the implementation Rationale: The involvement of stakeholders in the development of complex interventions is essential to ensure that the intervention and process are relevant, acceptable, and user friendly.
Specific objective: Describe the co-creation process and explore the needs and determinants of a midwife-led quality improvement targeting evidence-based midwifery practices.
Research Question: How do multisectoral stakeholders describe ways to implement the MIDWIZE model, how can the model be adapted to the local context and what strategies for implementation should be taken? (As the remaining parts of the intervention will be co-created, the following parts are preliminary)
Sub-study 2 - Implementation and evaluating the sustainability of the implementation Rationale: This study will explore how midwives can take the lead in implementing or enhancing evidence-based practical components of maternal care. Long-term sustainability is vital in order to maximise the potential benefits of implementation. Therefore, this study will, apart from measuring the midwives' QI projects' during the implementation phase, also measure the long-term impact six months after the project has ended. Based on the co-creation, the Midwize intervention targets three evidence-based practices where a gap between evidence and practice existed: dynamic birth positioning, empowering women in decision-making about birth positions, perineal protection, and intrapartum support. Spearheaded by a team of midwives known as the "Midwize Ambassadors," this seven-month quality improvement initiative was co-developed with expert guidance in quality enhancement and practical midwifery skills. Employing Plan-Do-Study-Act (PDSA) cycles aligned with the Model for Improvement framework, the intervention adopted a train-the-trainer methodology and conducted weekly online support sessions.
Aim: To investigate the process of a midwife-led QI intervention and the uptake of evidence-based midwifery practises.
Sub-study 3 - Outcomes Aim: To investigate the outcomes of a midwife-led QI intervention targeting evidence-based midwifery practises.
Sub-study 3 - Scaling up Aim: To explore how the Midwize intervention can be scaled up at other facilities in Kampala and what the health outcomes are for women and newborns.
Methodology Study Site Naguru maternity unit in Kampala, Uganda, is a public facility with 9000 births/year.
Study design and data collection The overall study design is a longitudinal observational study. Sub-Study 1
Focus Group Discussions (FGD) and workshops will be held in three steps:
- Clinical staff (e.g., midwives, nurses, obstetricians, and assistant nurses), stakeholders at professional associations, academia (e.g., midwife educators, researchers, and students), and decision-makers (e.g., staff at ministry of health and hospital managers) will be included (n=36, divided into six groups). Barriers and facilitators for multisectoral collaboration will be highlighted during the workshops.
- Members of the civil society (e.g., the projects main stakeholder - the childbearing women and their relatives) will be included in order to deliver an adequate and acceptable intervention (n=36, divided into six groups).
- Clinical staff and managers will be included to investigate the practical implementation aspects of the project and the birth unit's adherence to national policies and clinical guidelines (n=21, divided into three groups).
Sub-Study 2 Quantitative data will be collected during and after implementing the quality improvement components. The post-measurement data will be collected on the chosen components three and six months after project implementation to measure if the midwife-led quality improvement project has been sustained.
Data is collected through observations during birth and interviews with women.
Sub-study 3: Same data will be used as for Sub-study 2 Sub-study 4: Same as in sub-study 2 but at two new intervention sites and one control site.
Sample size Sub-Study 1 Part 1 - n=36 (Clinical staff, professional associations, academia, decision-makers) Part 2 - n=36 (childbearing women and their relatives) Part 3 - n=21 (clinical staff and managers) Sub-Study 2 and 3 As this is a quality improvement project, the number of participants depends on when the targeted goal is accomplished and the total number of participants can therefore not be decided on beforehand. The targeted goal for the specific unit will be decided in dialogue with staff and management.
However, a preliminary calculation with an estimated increase of the components by 25% would suggest a minimum of 266 women during the intervention and 266 women six months after the intervention to measure the long term sustainability.
Based on previous studies, the prevalence of the three components in connection with childbirth amounts to 50%. The size of the study population is based on a calculation with 80% strength and a 95% confidence interval. A clinically significant increase in the number of women giving birth with the three components of the intervention and who are satisfied with their delivery is estimated at 25%, i.e. from 50% of women to 75% of women. To achieve this level of strength, a study population of 242 women is required. With an estimated dropout rate of 10%, there will be a study population of 266 women. To study the project's long-term sustainability, a repeated measurement that includes 266 women six months after completing data collection 2 will be done.
Measurement during the implementation phase - n=266 (birthing women) Post measurement - n=266 (birthing women)
Sampling procedure Sub-Study 1 Part 1 - A targeted selection process will be applied, and people will be included based on experience, knowledge and position in the care system (i.e. decision-makers at different levels).
Part 2 - A random sampling will be made with stakeholders of the community (in this case, pregnant women or women who recently gave birth at the clinic) Part 3 - A targeted sampling with clinical staff and managers based on profession and experience
Sub-Study 2, 3 and 4 will include all women above the age of 18 with uncomplicated full-term pregnancies and births (i.e. between weeks 37 + 0 - 42 + 0).
Pre-testing No Pre-testing will be performed as this is a quality improvement project. The data collection for sub-study two will start when the implementation starts. The outcomes will be followed until sufficient data has been achieved.
Field editing of data The research midwife will fill in the data for sub-study 2, 3 and 4 in a data collection protocol, which will be entered electronically.
Missing data. The research midwife of the day will fill in any missing data in dialogue with the clinical staff. Missing data will be continuously monitored as the data sampling will be reported online (via a secured 2-step verification platform approved to share research data).
Data Management Computer packages to use. SPSS Quality control In the qualitative parts of the project, the trustworthiness of the data will be ensured by recording interviews and FGD, transcribing verbatim, triangulation by including other researchers in the team in the analysis, regular discussions on the analysis to reach a common understanding within the team.
The quantitative data quality will be checked by random control samples made by members of the research group. A statistician will be consulted during the analysis and an electronic logbook will be kept in order for external researchers to check the procedure.
Data Analysis Presentation of data The findings will be published in peer-reviewed academic journals.
Analysis Techniques Sub-Study 1 - Thematic analysis, according to Braun \& Clark (2006) Sub-Study 2, 3 and 4 - SPSS will be used for descriptive and comparative analysis of the data
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| The MIDWIZE model | – | Other: The MIDWIZE modelPregnant women giving birth during at Naguru maternity ward during the intervention period It's only Sub/study 2 in this PhD project which is a clinical trial and which is described onwards. Sub-study 2 will include all women above the age of 18 with uncomplicated full-term pregnancies and births (i.e. between weeks 37 + 0 - 42 + 0) giving birth at the delivery ward during the implementation phase. Data will be collected during the implementation of the quality improvement components. |
| The MIDWIZE model - postintervention | – | –Pregnant women giving birth at Naguru maternity ward 3 and 6 months post intervention period. Sub-study 2 will include all women above the age of 18 with uncomplicated full-term pregnancies and births (i.e. between weeks 37 + 0 - 42 + 0) giving birth at the delivery ward 3 and 6 months after the implementation phase. Data will be collected after implementing the quality improvement components. The post-measurement data will be collected on the chosen components six months after project implementation to measure if the midwife-led quality improvement project has been sustained. |
| The MIDWIZE model - scaling up | – | –The intervention will be scaled up at three additional sites and will include all women above the age of 18 with uncomplicated full-term pregnancies and births (i.e., between weeks 37 + 0 - 42 + 0) giving birth at the delivery ward during the implementation phase. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Pregnant women coming to give birth at Naguru Hospital during or after the implementation of the MIDWIZE model.
Key inclusion criteria (1 listed)
- People above the age of 18 with uncomplicated singleton full-term pregnancies and births (i.e. between weeks 37 + 0 - 42 + 0).
Key exclusion criteria (1 listed)
- People under the age of 18, people with complications in pregnancy or with a planned c-section.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| The MIDWIZE modelSo-called "MIDWIZE ambassadors" are planned to be appointed to lead the clinical implementation of the quality improvement components. Initial training workshops will be held with the ambassadors on practical aspects of the chosen components and how to explain their benefits to the units' staff. Training will also be provided on how to enhance interdisciplinary teamwork and coordinate quality improvements. The workshops will be held onsite at Naguru hospital and online via the project's "MIDWIZE virtual platform". The ambassadors will themselves hold training workshops to support midwives and other healthcare providers at the clinics during the implementation of the quality improvements components. The virtual MIDWIZE platform will contain videos, posters, presentations, and other training material that the ambassadors can utilise to enhance the units' capacity and engage their colleagues. | Other | The MIDWIZE model |
Primary outcome
The uptake of the midwives quality improvments
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Three evidence based midiwfery practises (i) dynamic birth positions, (ii) intrapartum support and (iii) prevetion of perineal tears .
Apgar score
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Apgar score. The Apgar score is a rapid assessment of a newborn's health, conducted one minute and five minutes after birth, evaluating their heart rate, respiratory effort, muscle tone, reflex irritability, and color. Each component is scored from 0 to 2 points, with a maximum score of 10 points.
Perineal tear
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Perineal tear (divided in unsutured tear, sutured tear, sphinkter tear)
Episiotomy
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Was episiotomy performed at birth
Postpartum haemorrhage
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Postpartum haemorrhage
Neonatal and maternal deaths
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Neonatal and maternal deaths
12 secondary outcomes
Mothers age
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Level of education
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Marital status
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Area of living
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Employment
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Obstetric background
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.6months after implementation phase is completed.
Gestation week
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Mode of delivery
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Length of second stage of labour
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Birth weight
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Transfer to a neonatal unit
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Skin-to-skin care
Time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Apr 2024.
- Background: PubMed 31801479Berta M, Lindgren H, Christensson K, Mekonnen S, Adefris M. Effect of maternal birth positions on duration of second stage of labor: systematic review and meta-analysis. BMC Pregnancy Childbirth. 2019 Dec 4;19(1):466. doi: 10.1186/s12884-019-2620-0.
- Background: PubMed 34648571Hailemeskel S, Alemu K, Christensson K, Tesfahun E, Lindgren H. Health care providers' perceptions and experiences related to Midwife-led continuity of care-A qualitative study. PLoS One. 2021 Oct 14;16(10):e0258248. doi: 10.1371/journal.pone.0258248. eCollection 2021.
- Background: PubMed 33275948Nove A, Friberg IK, de Bernis L, McConville F, Moran AC, Najjemba M, Ten Hoope-Bender P, Tracy S, Homer CSE. Potential impact of midwives in preventing and reducing maternal and neonatal mortality and stillbirths: a Lives Saved Tool modelling study. Lancet Glob Health. 2021 Jan;9(1):e24-e32. doi: 10.1016/S2214-109X(20)30397-1. Epub 2020 Dec 1.
- Results publication: PubMed 37930253Blomgren J, Wells MB, Erlandsson K, Amongin D, Kabiri L, Lindgren H. Putting co-creation into practice: lessons learned from developing a midwife-led quality improvement intervention. Glob Health Action. 2023 Dec 31;16(1):2275866. doi: 10.1080/16549716.2023.2275866. Epub 2023 Nov 6.
- Derived from this study: PubMed 39754106Blomgren J, Wells MB, Amongin D, Erlandsson K, Wanyama J, Afrifa DA, Lindgren H. Improving apgar scores and reducing perineal injuries through midwife-led quality improvements: an observational study in Uganda. BMC Public Health. 2025 Jan 3;25(1):19. doi: 10.1186/s12889-024-21137-w.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Helena Lindgren, PhD principal investigator
Karolinska Institutet
4 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Midwifery, run by Karolinska Institutet at 4 sites in Uganda.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 29 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 4 sites in Uganda. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Helena Lindgren (0733442599 ext. +46, helena.lindgren@ki.se), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The uptake of the midwives quality improvments (time frame: Through study completion, an average of 6 months and a follow up period (2 weeks) after 3 and 6months after implementation phase is completed.). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05237375, which also lists 5 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Apr 2024.