Prospective validation of a mobile health application for blood pressure management in patients with hypertensive disorders of pregnancy: study protocol for a randomized controlled trial

被引:1
作者
Kwun, Ju-Seung [1 ,2 ]
Choi, Jina [1 ,2 ]
Yoon, Yeonyee E. [1 ,2 ]
Choi, Hong-Mi [1 ,2 ]
Park, Jee Yoon [3 ]
Kim, Hyeon Ji [3 ]
Lee, Min Jung [3 ]
Choi, Bo Young [3 ]
Yoo, Sooyoung [4 ]
Suh, Jung-Won [1 ,2 ]
机构
[1] Seoul Natl Univ, Cardiovasc Ctr, Dept Internal Med, Bundang Hosp, 82,Gumi Ro 173 Beon Gil, Seongnam Si 13620, Gyeonggi Do, South Korea
[2] Seoul Natl Univ, Dept Internal Med, Seoul, South Korea
[3] Seoul Natl Univ, Bundang Hosp, Dept Obstet & Gynecol, Coll Med, Seongnam, South Korea
[4] Seoul Natl Univ, Healthcare ICT Res Ctr, Off eHlth Res & Businesses, Bundang Hosp, Seoul, South Korea
关键词
Hypertensive disorder of pregnancy; Mobile healthcare; Electronic medical records; Randomized controlled trial; UNITED-STATES; PREECLAMPSIA; OUTCOMES; WOMEN;
D O I
10.1186/s13063-024-08200-y
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundHypertensive disorders of pregnancy (HDP) pose significant risks to both maternal and fetal health, contributing to global morbidity and mortality. Management of HDP is complex, particularly because of concerns regarding potential negative effects on utero-placental circulation and limited therapeutic options due to fetal safety. Our study investigates whether blood pressure monitoring through a mobile health (mHealth) application can aid in addressing the challenges of blood pressure management in pregnant individuals with HDP. Additionally, we aim to assess whether this intervention can improve short-term maternal and fetal outcomes and potentially mitigate long-term cardiovascular consequences.MethodsThis prospective, randomized, single-center trial will include 580 pregnant participants who meet the HDP criteria or who have a heightened risk of pregnancy-related hypertension due to factors such as multiple pregnancies, obesity, diabetes, or a history of HDP in prior pregnancies leading to preterm birth. Participants will be randomized to either the mHealth intervention group or the standard care group. The primary endpoint is the difference in systolic blood pressure from enrollment to 1 month after childbirth. The secondary endpoints include various blood pressure parameters, obstetric outcomes, body mass index trajectory, step counts, mood assessment, and drug adherence.ConclusionsThis study emphasizes the potential of mHealth interventions, such as the Heart4U application, to improve blood pressure management in pregnant individuals with HDP. By leveraging technology to enhance engagement, communication, and monitoring, this study aims to positively impact maternal, fetal, and postpartum outcomes associated with HDP. This innovative approach demonstrates the potential of personalized technology-driven solutions for managing complex health conditions.Trial registrationClinicalTrials.gov NCT05995106. Registered on 16 August 2023.
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页数:12
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