Zahroh Rana Islamiah, Betrán Ana Pilar, Lauer Betrán Susana, Kaboré Charles, Bohren Meghan A
Gender and Women's Health Unit, Nossal Institute for Global Health, School of Population and Global Health, The University of Melbourne, Carlton, Australia.
UNDP-UNFPA-UNICEF-WHO-World Bank Special Programme of Research, Development and Research Training in Human Reproduction (HRP), World Health Organization, Geneva, Switzerland.
JMIR Res Protoc. 2025 Sep 8;14:e69808. doi: 10.2196/69808.
Assisted vaginal birth is a lifesaving procedure where health workers use special devices to expedite birth vaginally when some complications emerge, such as due to prolonged labor. When the use of assisted vaginal birth is possible and appropriate, it provides benefits over cesarean section. These benefits include shorter recovery, reduced hospital stays, lower risks of complications, cost savings, and greater likelihood of vaginal birth in future pregnancies. Despite these benefits, the use of assisted vaginal births has declined in recent years. Challenges remain on how to implement assisted vaginal birth effectively, equitably, and at scale in different health systems. Formative research is useful to understand local health system preparedness, acceptability, feasibility, and resource availability for designing and implementing health interventions.
We developed a generic formative research protocol that can be used to design and implement interventions to optimize use of assisted vaginal birth in any setting and context.
This formative research protocol is to be conducted in the setting where interventions to optimize assisted vaginal birth will be implemented. The formative research has three components: (1) document review, (2) readiness assessment, and (3) primary qualitative research. Document review will examine existing policy and guidelines, while readiness assessment will assess the service delivery context. The 2 components aim to identify potential barriers and facilitators to use of assisted vaginal birth. Primary qualitative research will involve women, families, community members, health workers, facility administrators, and policy makers. Interview questions are structured around potential interventions to optimize use of assisted vaginal birth. This protocol includes all the essential study instruments.
This is a generic research protocol that can be used by any stakeholder aiming to optimize assisted vaginal birth in any setting. Serving as a preparatory guide, it provides a structured approach for planning and implementing evidence-based and context-specific strategies aligned with best practices in maternal health care. No data collection or analysis has been conducted to date.
This generic protocol can serve as a guide in conducting formative research as intervention preparation to optimize use of assisted vaginal birth. The results can inform the design and implementation of appropriate interventions from the perspectives of important stakeholders. Therefore, we recommend that trialists, clinicians, researchers, administrators, and policy makers use this protocol before implementation to understand local context and incorporate perspectives of key stakeholders to promote equitable, high-quality, and women-centered care.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): PRR1-10.2196/69808.
阴道助产是一种挽救生命的操作,当出现一些并发症(如产程延长)时,医护人员使用特殊设备来加速经阴道分娩。当具备使用阴道助产的条件且适宜时,它比剖宫产更具优势。这些优势包括恢复时间更短、住院时间缩短、并发症风险降低、成本节约以及未来妊娠时经阴道分娩的可能性更大。尽管有这些优势,但近年来阴道助产的使用有所下降。在不同的卫生系统中,如何有效、公平且大规模地实施阴道助产仍存在挑战。形成性研究有助于了解当地卫生系统的准备情况、可接受性、可行性以及设计和实施卫生干预措施所需的资源。
我们制定了一份通用的形成性研究方案,可用于设计和实施干预措施,以优化在任何环境和背景下阴道助产的使用。
本形成性研究方案将在实施优化阴道助产干预措施的环境中进行。该形成性研究包括三个部分:(1)文献回顾,(2)准备情况评估,以及(3)初步定性研究。文献回顾将审查现有政策和指南,而准备情况评估将评估服务提供的背景。这两个部分旨在确定阴道助产使用的潜在障碍和促进因素。初步定性研究将涉及女性、家庭、社区成员、医护人员、机构管理人员和政策制定者。访谈问题围绕优化阴道助产使用的潜在干预措施展开。本方案包括所有必要的研究工具。
这是一份通用的研究方案,任何旨在在任何环境中优化阴道助产的利益相关者都可使用。作为一份准备指南,它为规划和实施基于证据且针对具体情况的策略提供了一种结构化方法,这些策略与孕产妇保健的最佳实践相一致。迄今为止尚未进行数据收集或分析。
这份通用方案可作为开展形成性研究的指南,作为干预准备以优化阴道助产的使用。研究结果可为从重要利益相关者的角度设计和实施适当的干预措施提供参考。因此,我们建议试验者、临床医生、研究人员、管理人员和政策制定者在实施前使用本方案,以了解当地情况并纳入关键利益相关者的观点,从而促进公平、高质量且以女性为中心的护理。
国际注册报告识别码(IRRID):PRR1-10.2196/69808