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Hill-Rom WAVE for Positional Obstructive Sleep Apnea at Home

Not Applicable
Terminated
Conditions
Sleep Apnea, Obstructive
Interventions
Device: Wave 4.3
Registration Number
NCT03971721
Lead Sponsor
Ohio State University
Brief Summary

1. Determine the effects of a mattress support (Wave 4.3) that promotes the avoidance of supine airway position at home on the apnea-hypopnea index (AHI) in patients with positional obstructive sleep apnea (OSA).

2. Determine the effects of Wave 4.3 on subjective measures of sleepiness and daytime function in patients with positional OSA.

3. Determine the effects of Wave 4.3 on subjective measures of sleep quality in patients with positional OSA.

Detailed Description

This is a preliminary single-arm study. The study will last up to 4 weeks including the screening period. Subjects will sleep using the mattress support at home for two consecutive weeks.

Outcome measures will include: AHI derived from HSAT (primary outcome), oxygen desaturation index (ODI), Epworth Sleepiness Scale (ESS) score, Functional Outcomes of Sleep Questionnaire (FOSQ), Visual Analog Scale (VAS) and questionnaire assessments of sleep quality, and actigraphic sleep measures. Subjects will also keep a sleep diary every night for the duration of the study. Subjects will be asked about their bed partners' report on snoring and witnessed apneas.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
3
Inclusion Criteria

  • • 18-75 years of age

    • Willing and able to give informed consent

    • Able to speak and understand English

    • Previous sleep study prior to enrollment done based on previous clinical evaluation by the subject's treating physician in the course of usual clinical care:

      1. overall AHI 5-40 events/hr.
      2. at least 10% time spent in the supine and 10% time in the non-supine positions.
      3. APOC I and APOC II
      4. central respiratory events < 50% of the total number of apneas and hypopneas

    • Using at least a queen-sized mattress when sleeping at home

    • Patients who meet the above criteria who have been prescribed CPAP or dental device but are non-adherent to treatment will be enrolled in the study. CPAP non-adherence will be defined as average nightly use < 4hrs/night based on a download of the CPAP machine, or self- acknowledged discontinuation or non-regular of CPAP use.

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Exclusion Criteria

  • • Incapable of giving informed consent

    • Under the age of 18

    • Active titration of medication

    • Pregnancy, lactation (will be screened with urine pregnancy test)

    • Self-reported Substance abuse (current)

    • Excessive alcohol consumption

      • Excessive alcohol use is defined as:
      • More than 3 glasses of wine a day
      • More than 3 beers a day
      • More than 60 mL of hard liquor a day

    • Use of home oxygen

    • Presence of severe daytime sleepiness defined as an Epworth sleepiness scale score > 16 or a prior history of falling asleep while driving

    • Presence of cardiac pacemaker or automatic implantable cardioverter-defibrillator (AICD).

    • Unstable medical problem such as uncontrolled hypertension.

    • Body Mass Index (BMI) >45 kg/m2

    • Any other clinically significant condition that, in the opinion of the investigators, might put the subject at risk of harm during the study or might adversely affect the interpretation of the study data.

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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Wave Mattress SupportWave 4.3The mattress support will be delivered at the subject's home by professional staff of the sponsor (Hill-Rom) in the presence of the research coordinator or investigator. The subject will sleep on mattress support for the duration of study participation.
Primary Outcome Measures
NameTimeMethod
Apnea-Hypopnea Index Difference Between Two Nights2 nights

Apnea-Hypopnea Index derived from Home Sleep Test. The apnea-hypopnea index (AHI) is the combined average number of apneas and hypopneas that occur per hour of sleep between two nights. AHI\<5 is indicative of no sleep apnea, AHI 5-15 is indicative of mild sleep apnea, AHI 15-30 is indicative of moderate sleep apnea, AHI\>30 is indicative of severe sleep apnea. The minimum AHI is 0, and there is no maximum. A higher score means a worse outcome. Subscales are not used to compute the value. The difference was calculated based on the value at night 1 minus the value at night 2 (converted to a positive value if the difference created a negative value). The mean value was calculated by adding the difference based on the total number of participants.

Secondary Outcome Measures
NameTimeMethod
Epworth Sleepiness ScoreCompleted at Visit 1 and Visit 4 (~5 minutes)

A subjective measure of sleepiness on average based on the total score. The score ranges from a minimum of 0 to a maximum of 24. A higher score means a worse outcome. Subscales are not used to compute the value. The difference was calculated based on the value at visit 1 minus the value at visit 4 (converted to a positive value if the difference created a negative value). The mean value was calculated by adding the difference based on the total number of participants.

Functional Outcomes of Sleep Questionnaire ScoreCompleted at Visit 2 and Visit 4 (~5 minutes)

A subjective measure of sleepiness on daytime function with an average of the total score. The score ranges from a minimum of 0 to a maximum of 20. A higher score means a better outcome. Subscales are not used to compute the value. The difference was calculated based on the value at visit 2 minus the value at visit 4 (converted to a positive value if the difference created a negative value). The difference was calculated based on the value at visit 2 minus the value at visit 4 (converted to a positive value if the difference created a negative value). The mean value was calculated by adding the difference based on the total number of participants.

Visual Analog Scale ScoreCompleted at Visit 2 and Visit 4 (~5 minutes)

A subjective measure of sleepiness with the average of the total score. The score ranges from a minimum of 0 to a maximum of 100. A higher score means a better outcome. Subscales are not used to compute the value. The difference was calculated based on the value at visit 2 minus the value at visit 4 (converted to a positive value if the difference created a negative value). The mean value was calculated by adding the difference based on the total number of participants.

Oxygen Desaturation Index Difference Between Two Nights2 nights

Oxygen Desaturation Index calculated based on the average between two nights measured. Desaturation episodes are generally described as a decrease in the mean oxygen saturation of ≥4% (over the last 120 seconds) that lasts for at least 10 seconds. ODI values can range from 0 to greater than 30. A higher score means a worse outcome. Subscales are not used to compute the value. The difference was calculated based on the value at night 1 minus the value at night 2 (converted to a positive value if the difference created a negative value). The mean value was calculated by adding the difference based on the total number of participants.

Trial Locations

Locations (1)

The Ohio State University

🇺🇸

Columbus, Ohio, United States

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