WELCOME: Digital transition of premature and newborn infants with special care needs to postdischarge care – study protocol for a randomised controlled duo-centred study

医学 协议(科学) 卫生服务研究 医疗急救 急诊医学 医疗保健 梅德林 流行病学 公共卫生 重症监护医学 家庭医学 儿科 随机对照试验 护理标准 研究设计 数字健康
作者
Laura Sehn,M.A.A. Westeneng den Otter,J.C. Ogilvie Will,Rosa M. S. Visscher,Sandra Kus,Michaela Coenen,Andreas W. Flemmer,Esther Schouten,Antje Tannen,Uli Fischer
出处
期刊:BMJ Open [BMJ]
卷期号:15 (10): e104346-e104346 被引量:2
标识
DOI:10.1136/bmjopen-2025-104346
摘要

INTRODUCTION: The transition from hospital to home can be challenging for parents of premature infants due to a lack of education on specific care. This may lead to both higher readmission rates and healthcare costs. Telehealth interventions can improve the quality of care specific to premature and critically ill newborns. This protocol outlines the WELCOME study and evaluates its feasibility and effectiveness of this approach. METHODS AND ANALYSIS: This two-centre randomised control trial (RCT) will assign 240 families with premature and critically ill newborns to an intervention or control group. The study has a parallel group design and an exploratory framework. The control group will receive standard postdischarge care. The intervention group will additionally receive scheduled video consultations, digital assessments and 24/7 access to educational resources. Primary outcomes will focus on 30-day readmission and emergency care use. Secondary outcomes will include child development and parental health. The intervention is expected to be feasible, with high acceptance and minimal drop-out. It will aim to improve parents' self-efficacy and health literacy. If successful, insights from this multimethod telehealth study will inform standard care. ETHICS AND DISSEMINATION: Results will be published in anonymised and summarised form in international and national journals and symposia. The study received ethical approval from the Ethics Committee of the Ludwig-Maximilians-University Munich (No. 25-0028) and was registered in the German Clinical Trials Register on 6 March 2025 (DRKS00034422). TRIAL REGISTRATION NUMBER: DRKS00034422.
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