Sleep Apnea Intervention for Cardiovascular Disease Reduction
This trial is active, not recruiting.
|Condition||obstructive sleep apnea|
|Treatments||conservative medical therapy, active pap with behavioral modification, sham pap, active pap with rt support|
|Sponsor||Brigham and Women's Hospital|
|Collaborator||Beth Israel Deaconess Medical Center|
|Start date||March 2011|
|End date||March 2014|
|Trial size||150 participants|
|Trial identifier||NCT01261390, 2010P002671|
Moderate to severe sleep apnea (a high number of breathing pauses on a sleep study) is a common health problem that is often associated with loud snoring and sleepiness.The medical term for this problem is obstructive sleep apnea (OSA). People with OSA often have an increased risk for developing heart disease or may already have a diagnosis of heart disease.
A clinical research study is being conducted at Brigham and Women's Hospital and Beth Israel Deaconess Medical Center to compare the effects of continuous positive airway pressure (CPAP) to conservative medical therapy with participation in one of four groups:
- CPAP Therapy Group: Standard medical treatment for sleep apnea, with CPAP mask worn during sleep. Participants randomized to either Respiratory Therapist (RT)only or RT with Cognitive Behavioral Therapist.
- Alternative CPAP Group: Different air delivery level from mask than CPAP Therapy Group. RT meetings.
- Conventional Medical Therapy (CMT) Group: Receive one year supply of nasal strips and follow guidelines for how to change sleep habits to minimize apnea.Frequent follow-up support with research coordinator.
A sleep doctor or cardiologist will have indicated that a potential participant is an appropriate candidate to receive CPAP or CMT as acceptable approaches to treat his/her sleep apnea. Participants will be recruited between the ages of 45-75 years who have diagnosed heart disease or between 55-75 years for those who have risk factors for developing heart disease.
This is a 12 month study* to evaluate alternative ways to address the potential for OSA treatment to reduce heart disease and to identify those features that would strengthen a later, large-scale randomized controlled trial.
*For those randomized after December 31, 2012, the study will be 6 months long.
We will test the hypothesis that active treatment for OSA with CPAP reduces CVD morbidity and mortality.
|Endpoint classification||safety/efficacy study|
|Intervention model||parallel assignment|
|Masking||double blind (subject, caregiver, investigator, outcomes assessor)|
Effectiveness of continuous positive airway pressure therapy on cardiovascular disease, using mean 24 hour systolic blood pressure as the trial's primary endpoint.
time frame: 3 years
Recruitment and retention rates of patients with moderate to severe obstructive sleep apnea and cardiovascular disease risk factors or established CVD participating in a controlled trial.
time frame: 3 years
Male or female participants from 45 years up to 75 years old.
Inclusion Criteria: - Obstructive apnea hypopnea index (AHI) ≥ 15 - Age 45-75 years, or 55 to 75 yrs if without established Cardiovascular Disease (CVD) - Ability to provide informed consent, with the patient and physician acknowledging accepting uncertainty on the role of PAP in CVD prevention. - Established CVD,or having diabetes mellitus, defined by one or more of the following: 1. Prior myocardial infarction 2. Coronary artery revascularization procedure (≥4 months before study entry) 3. Angiographically documented stenosis (>70%) of a major coronary artery 4. Prior ischemic stroke without major functional impairment 5. Diabetes mellitus treated with medication or ≥ 2 fasting glucose levels ≥ 126 mg/dl OR Three or more of the following established CVD risk factors: 1. Hypertension treated with medications or systolic BP > 140 or diastolic BP > 90 on ≥ 2 occasions 2. Male sex 3. BMI ≥ 30 4. Total cholesterol > 240 mg/dl or LDL cholesterol > 160 mg/dl or HDL < 45 mg/dl 5. > 10 pack years of smoking Exclusion Criteria: - Diagnosed heart failure with known cardiac ejection fraction of < 35% or NYHA class 3 or 4 status - Less than 4 months since MI, stroke or revascularization procedure - Poorly controlled hypertension (>170/>100) - Prior stroke with functional impairment interfering with ability to complete the protocol - Severe uncontrolled medical problems or medications that may influence measurements or impair ability to participate in the study exams (e.g. oral steroids; chronic opioid use; self- reported chronic kidney disease or, if measured, creatinine > 2.5 mg/dl of GFR < 30; anemia with Hgb < 10, etc.) - Resting oxygen saturation < 90% or nocturnal oxygen saturation <85% for > 10% of the sleep period; - Use of prescribed PAP for sleep apnea within the prior 2 years - Report of inability to spend >6 hrs in bed - Any use of prescribed PAP for sleep apnea - Severe sleepiness defined by an Epworth Sleepiness Score of >14 or report of falling asleep driving in the prior 2 years - Working as a professional driver - Low risk related to having sleep apnea defined by a Berlin Score < 2 - Central sleep apnea, with >50% of respiratory events classified as central apneas - Refusal to consider PAP use after an initial split-night PAP study (pre-randomization) - Concurrent involvement in another research study that will result in a conflict as determined by study doctors
|Official title||A Planning Study: Sleep Apnea Intervention for Cardiovascular Disease Reduction|
|Principal investigator||Susan Redline, MD, MPH|
|Description||In this pilot randomized controlled trial, we will assess the effectiveness of CPAP therapy to reduce the burden of cardiovascular disease (CVD) and CVD risk factors in patients with moderate to severe obstructive sleep apnea (OSA) presenting to a sleep disorders clinic. A total of 700 patients with a new diagnosis of moderate to severe OSA will be recruited from BWH-affiliated sleep disorder clinics, BWH, MGH, and Faulkner Hospital Cardiology Clinics (and similar specialized clinics seeing patients with cardiovascular risk factors, such as endocrinology and hypertensive clinics), Beth Israel Deaconess Medical Center and Joslin Diabetes Center. After completing a 2 week run-in period, randomized participants (approximately 150 participants will be randomized) will undergo baseline and 6 month assessments of key study exposure and outcome variables. Participants will be randomized after completion of Baseline visit. The treatment arms are as follows: The active groups are: - Active CPAP treatment delivered using standard respiratory therapist (RT) adherence education and support - Active CPAP treatment administered using adherence education and support delivered by a RT and enhanced by a behavioral promotion intervention The control arms are: - Sham-CPAP - CMT, alone Participants randomized before December 31, 2012 (n=108) also will undergo 12 month follow-up assessments. Participants will be offered a 12 month supervised conservative medical therapy (CMT) program for OSA over the duration of the study intervention. Subjects would be contacted at bimonthly intervals by alternating phone and office visits to assess safety, identify adverse events, identify health care utilization, and reinforce protocol adherence. At 6 and 12 months, study outcomes will be reassessed by collecting data from sources. Patients randomized after December 31, 2012 will undergo only 6 months of follow-up assessment. Participants will be offered a 6 month supervised conservative medical therapy (CMT) program for OSA over the duration of the study intervention. Subjects would be contacted at bimonthly intervals by alternating phone and office visits to assess safety, identify adverse events, identify health care utilization, and reinforce protocol adherence. At 6 months, study outcomes will be reassessed by collecting data from sources.|
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