Obstructive Sleep Apnea
Conditions
Keywords
Obstructive Sleep Apnea, Adherence, Chronic Disease, Telemedicine, Continuous Positive Airway Pressure, Mobile Health
Brief summary
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 (such as OSA) live healthier and more productive lives through better management of their conditions. Using an mHealth tool to help deliver the investigators' Self-Management intervention and improve the frequency and quality of patient-provider communications is a central component of that discovery process.
Detailed description
The objective of this proposal is to evaluate a new mobile health (mHealth) system for patients with Obstructive Sleep Apnea syndrome (OSA) that facilitates patient-centered, collaborative management for patients prescribed the first-line treatment, continuous positive airway pressure (CPAP). CPAP adherence rates are disappointingly low. The mHealth system proposed for use in the study is informed by the group's previous interventional efforts, including that of an interactive website intervention for OSA patients prescribed CPAP. Limitations of that intervention included use of an immobile desktop computer for website access and that it was not based on a previously evaluated protocol. The advantages to the proposed mHealth system are the use of a mobile device to allow for increased patient-provider communications and the incorporation of the Sleep Apnea Self-Management Program protocol. The evaluative aspect of this proposal is designed as a randomized, controlled clinical trial-Usual Care (control; UC); Self-Management Care (intervention 1; SM); Self-Management via mHealth (intervention 2; SM-Mobile). The key feature of the SM-Mobile intervention is the use of a mHealth tool that allows for the provision of the Self-Management Program through the utilization of audio/visual conferencing, self-monitoring, and treatment tracking with the patient remotely (i.e., in the non-clinic environment). The overarching aim of the present project is to examine the effect of this patient-centered, collaborative care intervention on improving the quality of care, and increasing CPAP adherence to a clinically meaningful level. The central questions that encompass the conceptual and empirical contours of the study: Does the SM-Mobile intervention have an effect on the patient's experience of care, CPAP adherence, and OSA outcomes relative to Usual Care and Self-Management Care? To answer these research questions, and in the process address fundamental intervention efficacy and cost issues in telemedicine, the proposed randomized, controlled trial aims specifically to achieve the following goals: This project has the following specific aims: Aim 1: To examine the effect of the Self-Management Care delivered by mHealth (SM-Mobile) intervention compared to Usual Care (SM) and Self-Management Care (SM) on level of CPAP adherence. The hypothesis is that participants in SM-Mobile group will exhibit higher levels of CPAP adherence compared to the UC and SM groups over the 2-month intervention period. Aim 2: To examine the effect of the SM-Mobile intervention, compared to Usual Care and Self-Management Care, on the patient's experience of the quality of patient-centered, collaborative care (as measured by the Patient Assessment of Chronic Illness Care and the CAHPS Clinician & Group Survey). The hypothesis is that participants in the SM-Mobile group will experience a greater improvement in patient-centered, collaborative care compared to the UC and SM groups over the 2-month follow-up period. Aim 3: To examine the effect of SM-Mobile, compared to UC and SM, on OSA apnea outcomes (e.g., OSA symptoms and OSA-specific health-related quality of life \[HRQOL\]). The hypothesis is that participants in the SM-Mobile group will experience greater improvements in self-reported OSA symptoms and HRQOL from baseline compared to the UC and SM over the 2-month follow-up period. Aim 4: To perform a basic cost analysis of the SM-Mobile intervention compared to Usual Care, applying a micro-cost methodology of measuring the quantity of inputs used in the production of care and the unit cost of each. This will be a test against the null hypothesis of no significant cost differences between groups.
Interventions
BEHAVIORALUsual Care
standard and typical CPAP educational and support protocol; is the base level education and support that is provided in the other two interventions in this study.
BEHAVIORALSelf-Management Care
Provision of sleep apnea-specific self-management education and support for those who are prescribed CPAP therapy
BEHAVIORALSelf-Management Mobile Care
Provision of sleep apnea-specific self-management education and support for those who are prescribed CPAP therapy via mobile phone
Sponsors
VA Office of Research and Development
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
The project will have a 4-year timeline. Patients and providers at both the VA Pulmonary Sleep Clinic will participate in this prospective randomized clinical trial. Patients will participate by completing written informed consent, agreeing to be randomized, completing a baseline assessment, participating in the study interventional protocol, and completing follow-up assessments up to one-year post-intervention. The intent is to recruit a study population that is fairly representative of the overall VASDHS population of patients diagnosed with OSA. To this end, inclusion criteria are designed to be as inclusive as possible and are operationalized as follows: * age \> 18 years; * confirmed diagnosis of OSA; * being newly prescribed CPAP therapy; and * having chronic symptoms as noted on screening symptom checklist. OSA diagnosis by the Sleep Clinic has been and is currently consistent with published consensus statements49 that CPAP treatment is indicated when the apnea-hypopnea index (AHI, number of apneas + hypopneas per hour of sleep) is either (1) greater than or equal to 15, or (2) between 5 and 15 AND accompanied by documented sleep apnea symptoms, including excessive daytime sleepiness, impaired cognition, mood disorders, insomnia, and documented cardiovascular diseases. Because mild OSA symptoms are at best modestly correlated with AHI, the research study will focus on patients with moderate to severe sleep apnea, and therefore inclusion criteria will require AHI \> 15.
Exclusion criteria
*
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Positive Airway Pressure Adherence | 2 month time point | objective measurement of the amount of time PAP therapy is used at the prescribed pressure |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Usual Care standard and typical PAP educational and support protocol
Usual Care: standard and typical CPAP educational and support protocol; is the base level education and support that is provided in the other two interventions in this study. | 131 |
| Self-Management Care Individualized self-management educational and support protocol
Self-Management Care: Provision of sleep apnea-specific self-management education and support for those who are prescribed CPAP therapy
Usual Care: standard and typical CPAP educational and support protocol; is the base level education and support that is provided in the other two interventions in this study. | 106 |
| Self-Management Mobile Care Individualized self-management educational and support protocol delivered in part by mobile health tool
Self-Management Mobile Care: Provision of sleep apnea-specific self-management education and support for those who are prescribed CPAP therapy via mobile phone
Usual Care: standard and typical CPAP educational and support protocol; is the base level education and support that is provided in the other two interventions in this study. | 111 |
| Total | 348 |
Baseline characteristics
| Characteristic | Usual Care | Total | Self-Management Mobile Care | Self-Management Care |
|---|---|---|---|---|
| Age, Continuous | 53.1 years STANDARD_DEVIATION 14 | 53.1 years STANDARD_DEVIATION 13.6 | 54.3 years STANDARD_DEVIATION 13.5 | 51.7 years STANDARD_DEVIATION 13.2 |
| Race (NIH/OMB) American Indian or Alaska Native | 2 Participants | 6 Participants | 2 Participants | 2 Participants |
| Race (NIH/OMB) Asian | 21 Participants | 52 Participants | 15 Participants | 16 Participants |
| Race (NIH/OMB) Black or African American | 25 Participants | 77 Participants | 32 Participants | 20 Participants |
| Race (NIH/OMB) More than one race | 3 Participants | 7 Participants | 4 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 1 Participants | 4 Participants | 3 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 79 Participants | 202 Participants | 55 Participants | 68 Participants |
| Region of Enrollment United States | 131 Participants | 348 Participants | 111 Participants | 106 Participants |
| Sex: Female, Male Female | 7 Participants | 30 Participants | 13 Participants | 10 Participants |
| Sex: Female, Male Male | 124 Participants | 318 Participants | 98 Participants | 96 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 116 | 0 / 89 | 0 / 91 |
| other Total, other adverse events | 0 / 116 | 0 / 89 | 0 / 91 |
| serious Total, serious adverse events | 0 / 116 | 0 / 89 | 0 / 91 |
Outcome results
Primary
Positive Airway Pressure Adherence
objective measurement of the amount of time PAP therapy is used at the prescribed pressure
Time frame: 2 month time point
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Usual Care | Positive Airway Pressure Adherence | 3.9 Hours | Standard Deviation 2.2 |
| Self-Management Care | Positive Airway Pressure Adherence | 3.9 Hours | Standard Deviation 2.4 |
| Self-Management Mobile Care | Positive Airway Pressure Adherence | 3.8 Hours | Standard Deviation 2.4 |