CompletedPhase 3Phase 4ACTRN12605000799651

A prospective, randomised controlled trial of auto-titrating Continuous positive airway pressure treatment for Obstructive Sleep Apnoea after acute Quadriplegia


Sponsor

Institute for Breathing and Sleep

Enrollment

150 participants

Start Date

Sep 17, 2009

Study Type

Interventional

Conditions

Summary

The COSAQ trial aims to establish the impact on sleep function of using a CPAP nasal mask and pump at night. Continuous positive airway pressure (CPAP) is a nasal/facial mask and machine used at night to treat sleep apnoea. Although CPAP is the usual treatment for sleep apnoea, previous reports suggest that is poorly tolerated in acute quadriplegia. A maximum of 35% of those with chronic quadriplegia are adherent with therapy, with a higher rate of 50% in acute quadriplegia. A range of factors including severe immobility and psychological factors appear to contribute to a low acceptance of CPAP. The SHiQ COSAQ project will examine the impact on sleep function, quality of life and cognition of using CPAP, and establish whether the benefit of using CPAP is outweighed by the inconvenience of using it. People with quadriplegia have extremely high rates of sleep apnoea after injury which is undoubtedly limiting their rehabilitation. Successful treatment may improve acute, sub-acute and community outcomes for this group and demonstrate significant cost-utility.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying A prospective, randomised controlled trial of auto-titrating Continuous positive airway pressure treatment for Obstructive Sleep Apnoea after acute Quadriplegia. You may be eligible if you are adults aged 18 and older with acute, traumatic quadriplegia. Participation typically involves medical assessments, possible treatment with the study intervention, and follow-up visits to track your health.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Three months of nightly, nocturnal continuous positive airway pressure and usual care. The devices are auto-titrating, therefore the amount of pressure delivered is that which is sufficient to maintai

Three months of nightly, nocturnal continuous positive airway pressure and usual care. The devices are auto-titrating, therefore the amount of pressure delivered is that which is sufficient to maintain a patent upper airway during sleep. Usual care is all other care provide to those with acute tetraplegia. This may include treatment for low lung volumes and retention of lung secretions.


Locations(2)

British Columbia, Canada

Multiple, United Kingdom

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ACTRN12605000799651