Impact of Sleep-Disordered Breathing Management in Systemic Hypertension Control: METASLEEP Project
NCT ID: NCT05986487
Last Updated: 2024-12-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
1523 participants
OBSERVATIONAL
2024-04-16
2025-12-31
Brief Summary
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Detailed Description
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The current model for managing patients with essential hypertension is based on deciding when to treat with measures that go beyond dietary and lifestyle interventions. Once it is decided to treat the patient pharmacologically, the ideal drug is decided and during follow-up whether it is necessary to change the treatment or not. This entire process is usually carried out by the Primary Care doctors. The hypertension specialist is usually reserved for difficult-to-control cases or patients with resistant hypertension. In the current model there is little communication between the different levels of care. In addition, the study of the SDB is carried out completely independently of this process. The METASLEEP project aims to change this work dynamic. The creation of the METASLEEP PC-node centralizes care for patients with hypertension in the Primary Care team (physician and nurse). The PC-node will evaluate the patient comprehensively, incorporating 24-hour ambulatory blood pressure monitoring as well as a sleep study. There will be coordination with the hypertension specialist for the management of complex cases and with the sleep unit specialist to support therapeutic decisions or management of patients with complex sleep apnea. Moreover, our project aims to incorporate the precision medicine techniques, such as the HIPARCO-score in the clinical management of hypertensive patients. Furthermore, the investigators aim to identify the best option that guarantees the best control in different clinical situations, with the greatest anticipation and with the fewest side effects, as well as with the greatest additional benefits and, finally, when to modify the treatment.
The METASLEEP project aims to contribute to the development of personalized medicine tools by identifying the molecular profile that enables to develop a non-invasive model with clinical utility. This model will contribute to the characterization of the patient that is vulnerable to the deleterious effects of OSA and who would benefit from OSA treatment to improve cardiovascular morbidity. The availability of an instrument based on a biomarker profile for risk stratification will help the physician to make therapeutic decisions in individuals with OSA and hypertension, contributing to the change of the current clinical management guidelines. Likewise, molecular tools can be developed to identify the profile of the patient that positively respond to CPAP treatment (in terms of blood pressure decrease). Finally, the investigators will obtain data that will evaluate the economic impact of the METASLEEP project. This cost-effectiveness analysis will be carried out from the perspectives of both, the SNS and the social perspective. Importantly, the investigators have planned a specific objective to define and calculate quantitatively, qualitative and cost-effectively the METASLEEP project, compared to the conventional current procedure.
The overall objective of the METASLEEP project is to establish a new paradigm in the treatment of hypertension through the management of sleep disordered breathing (SDB).
The specific objectives, are the following:
1. To implement the management of hypertension based on the presence of nocturnal hypertension and SDB (METASLEEP model).
2. To depict a singular cluster of circulating miRNAs (METASLEEP-score) in patients with nocturnal hypertension and SDB.
3. To characterize highly responder patients that would benefit from SDB treatment in terms of blood pressure control.
4. To implement in the clinical practice the use of the HIPARCO-score technology for the management of resistant hypertension.
5. To evaluate the feasibility and acceptability of the METASLEEP model for the comprehensive clinical management of hypertension based in the management of SDB.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with nocturnal hypertension and/or non-dipper pattern and diagnosed with OSA
Patients with nocturnal hypertension and/or non-dipper pattern who undergo a sleep test, obtaining the diagnosis of obstructive sleep apnea, will be treated following the clinical practice standards.
CPAP or usual practice
CPAP (continuous positive airway pressure) is a machine that uses mild air pressure to keep breathing airways open while you sleep.
Monitoring and intervention in follow-up
Each participating center can incorporate monitoring and intervention in the follow-up of patients into their work dynamics. Through the use of mobile applications, you can monitor the variables of: weight, diet, lifestyle, exercise and sleep. This intervention will help the patient to improve in different aspects of their health.
Patients with nocturnal hypertension and/or non-dipper pattern and without OSA
Patients with nocturnal hypertension and/or non-dipper pattern undergoing a sleep test, the result of which is negative for obstructive sleep apnea disease.
Monitoring and intervention in follow-up
Each participating center can incorporate monitoring and intervention in the follow-up of patients into their work dynamics. Through the use of mobile applications, you can monitor the variables of: weight, diet, lifestyle, exercise and sleep. This intervention will help the patient to improve in different aspects of their health.
Interventions
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CPAP or usual practice
CPAP (continuous positive airway pressure) is a machine that uses mild air pressure to keep breathing airways open while you sleep.
Monitoring and intervention in follow-up
Each participating center can incorporate monitoring and intervention in the follow-up of patients into their work dynamics. Through the use of mobile applications, you can monitor the variables of: weight, diet, lifestyle, exercise and sleep. This intervention will help the patient to improve in different aspects of their health.
Eligibility Criteria
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Inclusion Criteria
* Signature of the informed consent.
Exclusion Criteria
* Patients with very limiting chronic disease.
* Previous diagnosis of OSA or any other sleeping disorder
* Active treatment with CPAP.
* Fixed night shift worker.
18 Years
ALL
No
Sponsors
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Instituto de Salud Carlos III
OTHER_GOV
Sociedad Española de Neumología y Cirugía Torácica
OTHER
Responsible Party
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Ferran Barbe
Chair Respiratory Medicine
Principal Investigators
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Ferran Barbé Illa, MD
Role: PRINCIPAL_INVESTIGATOR
Spanish Respiratory Society (SEPAR)
Locations
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Hospital Universitari Arnau de Vilanova
Lleida, , Spain
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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PMP22/00030
Identifier Type: -
Identifier Source: org_study_id