LifeAPP: self-monitoring of blood pressure after preterm preeclampsia: a randomized controlled feasibility trial

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Autor(es): dc.contributorUniversidade Estadual Paulista (UNESP)-
Autor(es): dc.contributorUniversidade Estadual de Campinas (UNICAMP)-
Autor(es): dc.contributorEpidemiology and Clinical and Translational Research-
Autor(es): dc.contributorUniversity of Oxford-
Autor(es): dc.creatorKoike, Wilson-
Autor(es): dc.creatorCosta, Maria Laura-
Autor(es): dc.creatorGuida, José Paulo-
Autor(es): dc.creatorRoberts, James M.-
Autor(es): dc.creatorMartins, Ana Paula-
Autor(es): dc.creatorSoldá, Larissa Martinez-
Autor(es): dc.creatorDos Reis, Vitor Lira Vilela-
Autor(es): dc.creatorDos Santos, Tábata Regina Zumpano-
Autor(es): dc.creatorMcManus, Richard J.-
Autor(es): dc.creatorDe Oliveira, Leandro-
Data de aceite: dc.date.accessioned2025-08-21T19:35:33Z-
Data de disponibilização: dc.date.available2025-08-21T19:35:33Z-
Data de envio: dc.date.issued2025-04-29-
Data de envio: dc.date.issued2025-11-30-
Fonte completa do material: dc.identifierhttp://dx.doi.org/10.1080/10641955.2024.2439312-
Fonte completa do material: dc.identifierhttps://hdl.handle.net/11449/299367-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/11449/299367-
Descrição: dc.descriptionOBJECTIVE: This was a pilot study to investigate the feasibility of developing a low-cost mobile technology-based intervention to encourage blood pressure (BP) monitoring and adoption of healthy lifestyle habits. METHODS: This was a prospective, controlled, randomized, non-blinding feasibility study that involved the use of electronic BP monitor and smartphone. Eligible participants in the intervention group were instructed to send the BP measurements to members of the LifeAPP team digitally from an application for smartphones linked to the BP device by Bluetooth and also via WhatsApp. The LifeAPP team sent feedback containing information as follows: a) safety of the BP levels; b) motivational messages aiming at maintaining self-monitoring; c) motivational messages aiming at the importance of developing healthy lifestyle habits. The primary outcome was feasibility: recruitment capacity, retention, and compliance with follow-up rates. RESULTS: Between 1 June 2020 and 24 January 2021, 48 participants were randomized to the intervention group, and 48 participants were randomized to the control group. The recruitment capacity of the participating centers proved to be adequate. Among the participants recruited for intervention group, 21 (43.7%) attended predefined visits at 3 months and only 12 (25%) attended predefined visits at 6 months. Similar loss to follow-up was observed in the control group. CONCLUSION: Despite successful recruitment of a cohort of women following preterm preeclampsia, there was no sufficient retention of participants. Therefore, new strategies for long-term follow-up of women who developed preeclampsia are needed before a further study in this group of patients can be contemplated.-
Descrição: dc.descriptionObstetrics Department Botucatu Medical School Botucatu Sao Paulo State University-
Descrição: dc.descriptionDepartment of Obstetrics and Gynecology Faculty of Medical Sciences University of Campinas-
Descrição: dc.descriptionMagee-Womens Research Institute Department of Obstetrics and Gynecology Epidemiology and Clinical and Translational Research-
Descrição: dc.descriptionNuffield Department of Primary Care Health Sciences Radcliffe Primary Care University of Oxford-
Descrição: dc.descriptionObstetrics Department Botucatu Medical School Botucatu Sao Paulo State University-
Formato: dc.format2439312-
Idioma: dc.languageen-
Relação: dc.relationHypertension in pregnancy-
???dc.source???: dc.sourceScopus-
Palavras-chave: dc.subjectcardiovascular disease-
Palavras-chave: dc.subjectgestational hypertension-
Palavras-chave: dc.subjecthealthy lifestyle-
Palavras-chave: dc.subjectPreeclampsia-
Palavras-chave: dc.subjectself-monitoring of blood pressure-
Título: dc.titleLifeAPP: self-monitoring of blood pressure after preterm preeclampsia: a randomized controlled feasibility trial-
Tipo de arquivo: dc.typelivro digital-
Aparece nas coleções:Repositório Institucional - Unesp

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