Actively Recruiting
Impact of Remote Vital Signs Monitoring in People Using Long-term Oxygen Therapy
Led by University of Sao Paulo General Hospital · Updated on 2025-03-18
60
Participants Needed
1
Research Sites
57 weeks
Total Duration
On this page
Sponsors
U
University of Sao Paulo General Hospital
Lead Sponsor
A
Air Liquide SA
Collaborating Sponsor
AI-Summary
What this Trial Is About
Assess quality of life of patients using prolonged oxygen therapy
CONDITIONS
Official Title
Impact of Remote Vital Signs Monitoring in People Using Long-term Oxygen Therapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP),
São Paulo, São Paulo, Brazil, 05360-160
Actively Recruiting
Research Team
C
Celso RF Carval, Diretor do Estudo
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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