Development and evaluation of novel education and shared decision-making tools in women with Pre-eclampsia: multiple-site multiple-method investigation
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 300
- 试验地点
- 2
- 主要终点
- In pregnant women with lived experience of pre-eclampsia, effectiveness of the education and SDM tools, particularly with respect to timing of birth, will be measured using the Ottawa decisional conflict self report scale. Interaction tests will be used to look at differences in effect in different sub-groups (gestational age at time of intervention, parity, ethnicity, setting)
研究概览
简要总结
Title of the Research Project: Development and evaluation of educational and shared decision-making tools in women with pre-eclampsia: multiple-site multiple-method study.
Objectives:
- Co-design novel education and Shared Decision Making tools regarding: i) Information about pre-eclampsia during Pregnancy; ii) Shared decision making tool for planning time of birth in Pre-eclampsia; iii) Information about Postnatal care and Pre-eclampsia.
2. Describe introduction of tools into three different settings (India, Sierra Leone and Zambia).
3. Evaluate the impact of the novel tools based on aspects of the RE-AIM framework (Reach and effectiveness).
Pre-eclampsia continues to be a major cause of maternal and perinatal morbidity and mortality in India. The unpredictable disease progression, and the fact that affected women and their families do not understand the nature of the disease and importance of complying to treatment, makes management even more challenging.
This study hopes to develop education and shared decision-making (SDM) tools regarding antenatal management, timing of delivery and postnatal care in pre-eclampsia. We will include pregnant women, their relatives and healthcare providers in focus group discussions where they will be requested to give inputs into prototypes of SDM tools put together by the researchers.
The finalized SDM tools will be tested in clinal settings and their reach, effectiveness and acceptability will be assessed. The involvement of the patients, their relatives and healthcare personnel in the development of the aids, are likely to make them more appealing to all stakeholders.
With improved patient understanding about pre-eclampsia, we anticipate that they will have better compliance with clinical advice. This in the long run, is expected to decrease the morbidity and mortality associated with pre-eclampsia.
Setting and participants
Pregnant or postpartum women with pre-eclampsia and their principal healthcare professionals (obstetricians, paediatricians, midwives, community health workers), community stakeholders, in three healthcare settings (India, Sierra Leone, Zambia).
This study will be done in two sites in India with differing socio-cultural environment, language, and healthcare infrastructure.
The study sites are 1. Bagalkot, Karnataka and 2. Puri, Odisha.
Health condition studied: Pre-eclampsia Knowledge
Project design and methods:
Mixed methods study
Tools’ Development: Focus Group Discussions
Tools’ Evaluation: Focus Group Discussions; decisional conflict and acceptability questionnaires.
Study Duration: 12 months
Expected Outcome:
The study hopes to develop shared decision-making tools which will aid in the complex counselling required for effective management of pre-eclampsia. By aiding the understanding of the patients and the relatives about pre-eclampsia, it is anticipated that they will be more ready to comply with treatment and more equipped to take informed decisions during management. If the study proves that healthcare providers find the SDM tools useful in clinical settings, the tools could be adapted for use in different regions of India. Overall, we hope that development and use of the SDM tools decreases the morbidity and mortality associated with pre-eclampsia in the long run.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18.00 Year(s) 至 65.00 Year(s)(—)
- 性别
- All
入选标准
- •Women who have pre-eclampsia, their significant others, and healthcare personnel caring for such women will be included in Focus Group Discussions for the development of Shared Decision making tools.
- •In the second phase of the study, the impact of the developed tools will be evaluated in clinical situations by involving women with pre-eclampsia and healthcare personnel.
排除标准
- •Women/ patients who do not have pre-eclampsia.
结局指标
主要结局
In pregnant women with lived experience of pre-eclampsia, effectiveness of the education and SDM tools, particularly with respect to timing of birth, will be measured using the Ottawa decisional conflict self report scale. Interaction tests will be used to look at differences in effect in different sub-groups (gestational age at time of intervention, parity, ethnicity, setting)
时间窗: End of the study (at 1 year)
次要结局
- Post-intervention surverys will access acceptability amongst all participants(End of the study (1 year))
研究者
Dr Geetanjali Katageri
BVVS S Nijalingappa Medical College and HSK Hospital and Research Centre
