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Obstructive Sleep Apnoea clinical trials

View clinical trials related to Obstructive Sleep Apnoea.

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NCT ID: NCT04262986 Recruiting - Overweight Clinical Trials

A Brief Lifestyle Modification Programme in Overweight Subjects With Obstructive Sleep Apnoea - Needs Assessment

Start date: May 11, 2020
Phase:
Study type: Observational

Obstructive sleep apnea (OSA) is a common chronic disease and associated with cardiovascular and neurocognitive sequelae. Overweight is a common, reversible risk factor of OSA, and the rapid rise in obesity worldwide may lead to increases in OSA and related adverse health outcomes. Weight-loss interventions, especially comprehensive lifestyle interventions, are associated with improvements in OSA severity, cardiometabolic comorbidities, and quality of life. However, the intensive nature of these programmes often pose a barrier to adherence. Furthermore, although there is strong evidence to support the value of mobile text messaging to promote physical activity and healthy eating in clinical and community settings, messaging has rarely been applied in interventions for overweight OSA subjects. The proposed study aims to examine the feasibility of a brief lifestyle modification programme that makes use of smartphone technology (WhatsApp or WeChat) to empower subjects to start doing simple and easy-to-do exercises that can be easily integrated into daily life for gradual lifestyle change.

NCT ID: NCT01829854 Recruiting - Clinical trials for Obstructive Sleep Apnoea

To Investigate the Incidence of Obstructive Sleep Apnoea in Patient Undergoing Open Heart Surgery

Start date: June 2012
Phase: N/A
Study type: Observational

This is a study to investigate the incidence of Obstructive Sleep Apnoea in Patient undergoing open heart Surgery . This will include enrolment of 400 patient undergoing open heart surgery .

NCT ID: NCT01685736 Recruiting - Hypertension Clinical Trials

Ambulatory Versus Home Blood Pressure Monitoring in Obstructive Sleep Apnea

OSA
Start date: February 2012
Phase: N/A
Study type: Observational

Subjects referred to a sleep clinic had polysomnography (PSG), clinic BP measurements, 24-hour ABP monitoring and HBP monitoring using a device (Microlife WatchBP HomeN) that allows daytime (3 days, 2 duplicate readings/day) and automated nighttime BP measurement (3 nights, 3 readings/night).