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RECRUITINGINTERVENTIONAL

Impact of Remote Vital Signs Monitoring in People Using Long-term Oxygen Therapy

Impact of Remote Vital Signs Monitoring in People Using Long-term Oxygen Therapy : a Randomized Clinical Trial

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Assess quality of life of patients using prolonged oxygen therapy

Who May Be Eligible (Plain English)

Who May Qualify: - Patients with a clinical, radiological and/or anatomopathological diagnosis of COPD and ILD according to the 2020 ATS/JRS/ALAT guidelines; - Age over 18 years; - Clinical stability (absence of exacerbations or hospitalizations related to the underlying disease) for at least 6 weeks; - Patients who are on optimized drug therapy, including long-term home oxygen therapy (LTOT) - Have a smartphone compatible with the monitoring device; - Signing of the ICF to participate in the study. Who Should NOT Join This Trial: - Presence of other concomitant lung diseases; - Myocardial infarction within four months prior to the start of the study, unstable angina or severe heart disease (NYHA functional class III-IV) and/or decompensated. - Patients who received a lung transplant during the study - Living outside the coverage area or moving out of state Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Patients with a clinical, radiological and/or anatomopathological diagnosis of COPD and ILD according to the 2020 ATS/JRS/ALAT guidelines; * Age over 18 years; * Clinical stability (absence of exacerbations or hospitalizations related to the underlying disease) for at least 6 weeks; * Patients who are on optimized drug therapy, including long-term home oxygen therapy (LTOT) * Have a smartphone compatible with the monitoring device; * Signing of the ICF to participate in the study. Exclusion Criteria: * Presence of other concomitant lung diseases; * Myocardial infarction within four months prior to the start of the study, unstable angina or severe heart disease (NYHA functional class III-IV) and/or decompensated. * Patients who received a lung transplant during the study * Living outside the coverage area or moving out of state

Treatments Being Tested

BEHAVIORAL

Group Monitoring

In the intervention group (IG), participants receive a HR and SPO2 monitor watch and a pulse oximeter and will be monitored every 15 days by a nurse to check for non-adherence and/or technical failure, and/or exacerbations, and monthly to apply questionnaires.

BEHAVIORAL

Control Group

In the control group (CG), participants receive only a pulse oximeter and will be monitored monthly by a nurse to administer the questionnaires.

Locations (1)

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP),
São Paulo, São Paulo, Brazil