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Impact of the implementation of a telemedicine program on patients diagnosed with asthma.
Cabrerizo-Carreño, Héctor; Muñoz-Esquerre, Mariana; Santos Pérez, Salud; Romero-Ortiz, Ana Maria; Fabrellas, Núria; Guix-Comellas, Eva Maria.
Afiliação
  • Cabrerizo-Carreño H; Bellvitge University Hospital, Department of Pulmonary Medicine, L'Hospitalet de Llobregat, Catalunya, ES, Spain.
  • Muñoz-Esquerre M; Department of Fundamental and Medico-Surgical Nursing, Nursing School, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Catalunya, ES, Spain.
  • Santos Pérez S; Pneumology Research Group, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Catalunya, ES, Spain.
  • Romero-Ortiz AM; Bellvitge University Hospital, Department of Pulmonary Medicine, L'Hospitalet de Llobregat, Catalunya, ES, Spain. mmunoze@bellvitgehospital.cat.
  • Fabrellas N; Pneumology Research Group, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Catalunya, ES, Spain. mmunoze@bellvitgehospital.cat.
  • Guix-Comellas EM; Facultat de Medicina i Ciències de la Salut, University of Barcelona, L'Hospitalet de Llobregat, Catalunya, ES, Spain. mmunoze@bellvitgehospital.cat.
BMC Pulm Med ; 24(1): 32, 2024 Jan 13.
Article em En | MEDLINE | ID: mdl-38216971
ABSTRACT

BACKGROUND:

Asthma is one of the most common respiratory ailments worldwide. Despite broad understanding of the illness and of the available therapeutic options for it, patients with serious asthma suffer poor monitoring of their illness in 50% of cases.

AIM:

To assess the impact of the implementation of a mobile application (ESTOI) to control asthma in patients diagnosed with the illness, their adherence to treatment, and their perceived quality of life.

METHODOLOGY:

Randomized clinical trial with 52 weeks' follow-up of patients with asthma seen in a specialized hospital for their treatment in Spain. Some 108 included patients will be divided into two groups. The intervention group will undergo more exhaustive follow-up than normal, including access to the ESTOI application, which will have various categories of attention control of symptoms, health recommendations, current treatment and personalized action plan, PEF record, nutritional plan, and chat access with a medical team. The asthma control questionnaire ACT is the main assessment variable. Other variables to be studied include an adherence test for the use of inhalers (TAI), the number of exacerbations, maximum exhalation flow, exhaled nitric oxide test, hospital anxiety and depression scale, asthma quality-of-life questionnaire, forced spirometry parameters (FVC, FEV1, and PBD), and analytic parameters (eosinophilia and IGE). The data will be collected during outpatient visits. TRIAL REGISTRATION This trial has registered at ClinicalTrials.gov (Identifier NCT06116292).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Telemedicina Limite: Humans Idioma: En Ano de publicação: 2024

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Telemedicina Limite: Humans Idioma: En Ano de publicação: 2024