Actively Recruiting
Effectiveness of an E-health Intervention in Patients With Obstructive Sleep Apnoea
Led by Universitat de Lleida · Updated on 2024-05-10
260
Participants Needed
1
Research Sites
82 weeks
Total Duration
On this page
Sponsors
U
Universitat de Lleida
Lead Sponsor
I
Institut de Recerca Biomèdica de Lleida
Collaborating Sponsor
AI-Summary
What this Trial Is About
Obstructive sleep apnoea is a highly burdensome condition that not only impairs function but also confers a risk of cardiovascular disease. This is particularly evident among those who are poorly compliant with continuous positive airway pressure ventilation therapy. In the management of a chronic and frequent pathology such as OSA, it is necessary to have personalized programs that implement new technology-based tools to improve the comprehensive management of the patient in order to reduce the morbidity associated with this disease.
CONDITIONS
Official Title
Effectiveness of an E-health Intervention in Patients With Obstructive Sleep Apnoea
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Moderate obstructive sleep apnea with apnea-hypopnea index (AHI) between 15 and 30
- Diagnosed hypertension confirmed by 24-hour ambulatory blood pressure monitoring
- Men and women aged 18 years or older
- Ability to read, write, and speak Spanish and/or Catalan
- Currently living in Lleida, Spain
- Own or have access to a mobile phone with Android or iOS operating system
You will not qualify if you...
- Previous diagnosis of obstructive sleep apnea or use of continuous positive airway pressure (CPAP)
- Pregnancy
- Body mass index (BMI) below 17
- Currently undergoing bariatric surgery or waiting for the procedure
- Unable to complete questionnaires
- Unable to use technology
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Biomedical Research Institure of Lleida
Lleida, Spain, 25198
Actively Recruiting
Research Team
O
Oriol o Martínez-Navarro
CONTACT
F
Fran Valenzuela-Pascual
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
TREATMENT
Number of Arms
2
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