CPAP Therapy Support for Stroke and Sleep Apnea

Stroke and CPAP Outcome Study 3 Randomized Controlled Trial

Recruiting N/A Interventional Study
Stroke Patients CPAP OSA - Obstructive Sleep Apnea
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
250 (estimated)
Sponsor
University of Washington · Other
Who this trial is looking for

This trial is looking for stroke patients who have obstructive sleep apnea. Participants will receive support for using a CPAP machine during their rehabilitation.

Are You a Good Fit for This Trial?
Rules you out Active sedation that interferes with OSA testingRisk of aspiration from CPAP use

You may be able to join if

  • I am 18 years or older
  • I have had a stroke within the last 30 days
  • I can provide consent in English or Spanish

You may not be able to join if

  • I cannot provide consent in English or Spanish
  • I am currently in prison
  • I am pregnant
  • I use ventilators or high amounts of oxygen
  • I used CPAP in the 14 days before my stroke
  • I have serious lung conditions that limit CPAP use
  • I had a stroke due to tumors or blood vessel issues
  • I have had recent cranial or spinal surgery

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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About This Trial
The SCOUTS 3 study aims to test the effectiveness of an intensive CPAP (Continuous Positive Airway Pressure) therapy support program compared to usual care in stroke patients with obstructive sleep apnea (OSA) during inpatient rehabilitation (IPR). The study is a multicenter randomized controlled trial (RCT) involving recruitment of about 250 participants across two institutions and randomization…
Trial Locations
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Eligibility Criteria
Inclusion criteria include: 1. Age 18 years or older 2. Head CT or brain MRI demonstrating an acute ischemic infarction or intraparenchymal hemorrhage within past 30 days 3. Person providing consent (patient or legally authorized representative (LAR)) able to be consented in English or Spanish. Ex…
Contacts

Belqeis Abatiyow, BS

2067446067

babatiyo@uw.edu

CONTACT

Sandeep Khot, MD, MPH

2067448028

skhot@uw.edu

CONTACT