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Comparative Effectiveness Research to Enhance Outcomes in African-Americans With Obstructive Sleep Apnea

Primary Purpose

Obstructive Sleep Apnea

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Portable monitoring
Polysomnography
Home portable monitoring
Laboratory portable monitoring
Sponsored by
University of Illinois at Chicago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Obstructive Sleep Apnea focused on measuring OSA, portable monitoring, home diagnosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male and Female African-Americans (age ≥18 years)
  2. Berlin Questionnaire
  3. Ability to understand written and verbal English

Exclusion Criteria:

  1. Past treatment of OSA (medical, dental, or surgical)
  2. Other primary sleep disorder(s) by history
  3. Active uncontrolled medical conditions/immobility
  4. Current drug or significant alcohol use
  5. No current residential address or contact phone number

Sites / Locations

  • Sleep Science Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

OSA testing

Arm Description

Cross-over design, single group/arm Interventions: polysomnography with simultaneous portable monitoring and home portable monitoring administered to each participant in random order.

Outcomes

Primary Outcome Measures

Apnea Hypopnea Index (AHI)
AHI is the number of abnormal respiratory events (apneas and hypopneas) per hour of sleep. AHI on home portable monitor (PM) compared to AHI on laboratory polysomnography (PSG).

Secondary Outcome Measures

Technical Failure Rate
home PM tests that failed to provide technically adequate data for diagnosis. Technical failure(s) were tests where estimated total sleep time (TST) was ≤ 2 hours or portable monitor data of interpretable quality was less than 4 hours per recording.

Full Information

First Posted
November 22, 2013
Last Updated
May 20, 2014
Sponsor
University of Illinois at Chicago
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT01997723
Brief Title
Comparative Effectiveness Research to Enhance Outcomes in African-Americans With Obstructive Sleep Apnea
Official Title
Comparative Effectiveness Research to Enhance Outcomes in African-Americans With Obstructive Sleep Apnea
Study Type
Interventional

2. Study Status

Record Verification Date
May 2014
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Illinois at Chicago
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Obstructive Sleep Apnea (OSA) is under-diagnosed and is associated with increased cardiovascular morbidity and mortality. Laboratory-based overnight polysomnography (PSG) is the gold standard in clinical practice to diagnose OSA but has availability, cost, and resource limitations. In the last decade, an alternative diagnostic strategy, Portable Monitoring (PM) has emerged with the goal of reducing expense and delays in clinical management. In contrast to PSG, PM maybe performed unattended in homes, utilize different neurophysiologic and cardiorespiratory parameters, and may synthesize these data differently. PM is feasible and is approved by Centers for Medicare and Medicaid Services (CMS) in the United States. However, the diagnostic utility of PM in minority and underserved populations is not defined. African-Americans are more severely affected by hypertension and cardiovascular disease (CVD) than other ethnic groups and OSA is more common in this population. OSA is a treatable cause of hypertension. Despite this the impact of timely interventions for OSA on health outcomes and risk reduction specific to African Americans is unknown. Purpose of this research: In view of the vulnerability of this population and the potential for improvement in healthcare access for OSA with home-based diagnosis, this study aims to establish the feasibility and identify the potential advantages and limitations of home-based diagnosis of OSA in a high-risk urban African-American population including veterans with frequently limited access to healthcare. Hypothesis: The investigators hypothesize that home-based PM is not inferior to standard laboratory-based PSG in effectively diagnosing OSA in urban African Americans.
Detailed Description
Hypothesis: The investigators hypothesize that home-based PM is not inferior to standard laboratory-based PSG in effectively diagnosing OSA in urban African Americans. The specific aims of this project are: Primary Aims: Aim 1. To compare the validity of a comprehensive and current PM technology to standard in-laboratory full PSG 1a) to measure and compare diagnostic accuracy of home-based PM with laboratory-PSG b) to measure and compare diagnostic accuracy of simultaneous laboratory-based PM with laboratory-PSG Aim 2. To test the reliability and examine the applicability of PM in the home-setting a) to compare diagnostic accuracy of home-based PM with laboratory-based PM 2b) to examine factors associated with technical reliability (data failure rate) of home-based PM 2c) to compare patient satisfaction and preference of testing in home-setting to laboratory-setting

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnea
Keywords
OSA, portable monitoring, home diagnosis

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
OSA testing
Arm Type
Experimental
Arm Description
Cross-over design, single group/arm Interventions: polysomnography with simultaneous portable monitoring and home portable monitoring administered to each participant in random order.
Intervention Type
Device
Intervention Name(s)
Portable monitoring
Other Intervention Name(s)
WatchPAT200, Itamar medical Inc.
Intervention Description
A device applied over 1 arm (on the wrist and finger), worn overnight by patients to detect OSA.
Intervention Type
Other
Intervention Name(s)
Polysomnography
Intervention Description
One attended diagnostic sleep study.
Intervention Type
Device
Intervention Name(s)
Home portable monitoring
Intervention Description
Portable monitoring with WP200 device - applied by participants once at home.
Intervention Type
Device
Intervention Name(s)
Laboratory portable monitoring
Intervention Description
Portable monitoring with WP200 device - applied by technologist once in the laboratory simultaneously with polysomnography.
Primary Outcome Measure Information:
Title
Apnea Hypopnea Index (AHI)
Description
AHI is the number of abnormal respiratory events (apneas and hypopneas) per hour of sleep. AHI on home portable monitor (PM) compared to AHI on laboratory polysomnography (PSG).
Time Frame
4 days
Secondary Outcome Measure Information:
Title
Technical Failure Rate
Description
home PM tests that failed to provide technically adequate data for diagnosis. Technical failure(s) were tests where estimated total sleep time (TST) was ≤ 2 hours or portable monitor data of interpretable quality was less than 4 hours per recording.
Time Frame
4 days
Other Pre-specified Outcome Measures:
Title
Percentage of Participants Who Prefer Home Testing Over Laboratory Testing
Description
Participants indicated which test (PM or PSG) they preferred.
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and Female African-Americans (age ≥18 years) Berlin Questionnaire Ability to understand written and verbal English Exclusion Criteria: Past treatment of OSA (medical, dental, or surgical) Other primary sleep disorder(s) by history Active uncontrolled medical conditions/immobility Current drug or significant alcohol use No current residential address or contact phone number
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bharati Prasad, MD
Organizational Affiliation
University of Illinois at Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sleep Science Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
25126034
Citation
Garg N, Rolle AJ, Lee TA, Prasad B. Home-based diagnosis of obstructive sleep apnea in an urban population. J Clin Sleep Med. 2014 Aug 15;10(8):879-85. doi: 10.5664/jcsm.3960.
Results Reference
derived

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Comparative Effectiveness Research to Enhance Outcomes in African-Americans With Obstructive Sleep Apnea

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