Self-Management of Continuous Positive Airway Pressure Settings (ImPRESS)

  • End date
    Apr 30, 2023
  • participants needed
  • sponsor
    VA Office of Research and Development
Updated on 11 July 2022
continuous positive airway pressure


Obstructive sleep apnea (OSA) is a major chronic condition affecting the quality of life of millions of Americans. Per the Institute of Medicine new treatment adherence strategies are needed to help improve the quality of care, reduce social and economic costs, and help those with chronic conditions, including OSA, live healthier and more productive lives through better management of their conditions. Adherence with continuous positive airway pressure (PAP) therapy is disappointingly low, and new methods to increase both the use and efficacy of therapy are needed. Historically, patients have not been formally instructed to adjust their pressure settings on their PAP devices; practically, however, allowing patients to adjust their pressure settings fosters engagement, self-confidence, and control with therapy.


Because of clinical demands, patients are often under-educated and under-supported about the features of their positive airway pressure (PAP) devices. The most engaged patients are ones who understand the details of their device and change the feature settings so that they can maximize the benefits of therapy. Features settings include humidification level, expiratory pressure relief, pressure ramping, mask alert, auto pressure start, among other important comfort features. Historically, patients have not been provided with access to alter or modify therapy pressure settings, which requires physician prescription. Allied medical staff can carry out subsequent pressure setting changes. It is clear that it is difficult for the healthcare system to engage in optimal chronic disease management, and accommodate the needs of sleep apnea patients early in the treatment initialization process, which requires multiple visits/contacts to ensure that patients are maximizing the use of therapy.

The overarching aim of the proposed project is to examine the effect of providing patients with the ability to adjust their PAP pressure levels on therapy adherence and outcomes. To answer these research questions, the proposed randomized, controlled two-group trial of Sleep Apnea Self-Management Program (SM) and SM plus Individualized Pressure Adjustment (IPA) has the following specific aims related to APAP adherence and efficacy, patient-reported outcomes, and utilization: (1) To examine the effect of Individualized Pressure Adjustment (IPA) of settings on treatment adherence and efficacy (i.e., mask leak and residual apnea-hypopnea index); (2) To examine the effect of SM+IPA versus SM on patient self-reported treatment outcomes; and (3) To describe the effects of SM-IPA and SM groups on utilization.

Sleep apnea is one of the most common chronic conditions in the VA. Positive airway pressure (PAP) therapy is the gold-standard therapy for sleep apnea, but adherence with PAP is suboptimal. VA sleep programs are understaffed relative to clinical demand for education and support. While adaption to PAP therapy has traditionally been achieved through sequential visits and pressure changes initiated by providers during office-based care, self-monitoring and individualized pressure adjustment is an important strategy that would empower Veterans to achieve better control of their OSA. The key impacts of this project are significant for both patients (improved outcomes) and the VA (improved staff efficiencies).

While patients have control over a wide range of comfort features on their PAP devices, historically they have not been formally educated and supported to adjust pressure settings. The unique aspect of this study is the focus on individualizing pressure settings to allow for the maximizing therapeutic benefit, including increased PAP adherence. Importantly, this is done within the context of provider oversight.

The proposed study is a 6-month randomized, controlled, non-blinded, single-center study comparing the Sleep Apnea Self-Management Program (SM) to SM plus Individualized Pressure Adjustment (IPA). Both groups will receive the SM protocol to ensure that they receive identical OSA and PAP education and support. Participants in the intervention arm will be provided with additional education and support that will allow them to adjust their PAP pressures.

Positive findings from this study will result in a Toolkit that can be distributed to provide patients and providers with the knowledge necessary to improve the clinical management of OSA.

Condition Obstructive Sleep Apnea
Treatment Sleep Apnea Self-Management Program
Clinical Study IdentifierNCT03536572
SponsorVA Office of Research and Development
Last Modified on11 July 2022


Yes No Not Sure

Inclusion Criteria

The investigators' intent is to recruit a study population that is representative of
patients diagnosed with OSA. To this end, entry criteria are as inclusive as possible and
operationalized as follows
confirmed diagnosis of OSA
being newly prescribed an OSA therapy
having chronic symptoms per screening symptom checklist
fluency in English
receiving medical care at VA San Diego Healthcare System
OSA diagnosis by the investigators' Pulmonary Sleep Program has been and is currently
consistent with published consensus statements50 that therapy is indicated when the
apnea-hypopnea index (AHI, number of apneas + hypopneas per hour of sleep) is either (1)
>30 or (2) 5-30 AND accompanied by documented OSA symptoms, including EDS, impaired
cognition, mood disorders, insomnia, or documented cardiovascular diseases. Because sleep
apnea is of increasing importance in women, the investigators' plan is to oversample women
by 50% so that they represent 15% of the final study sample

Exclusion Criteria

Criteria for exclusion include
cognitive impairment sufficient to cause inability to complete the protocol (e.g
documented MMSE < 24/30)
low health literacy
residence in a geographical area outside of San Diego County (which could make some
fatal comorbidity (life expectancy <6 months as indicated by treating physician)
necessary in-person visits difficult)
significant documented substance/chemical abuse
clinical needs of patient outweighs needs of research study
other participant circumstances or characteristics that, in the opinion of a consensus
of study team, would interfere with the safety of a prospective participant or their
need for treatment (i.e.,:)
No exclusion criteria or any other study design elements will be used directly or
indirectly to restrict study participation by women or members of minority groups. Some
minority groups are thought to have higher OSA prevalence rates than Caucasians, so
assuming they are being screened/diagnosed at the same rates as Caucasians, the
investigators expect minority groups to be included in the study at levels equal to or
higher than the VA San Diego minority composition
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