TY - JOUR
T1 - SleepWell24, a Smartphone Application to Promote Adherence to Positive Airway Pressure Therapy
T2 - Feasibility and Acceptability in a Randomized Controlled Trial
AU - Petrov, Megan E.
AU - Epstein, Dana R.
AU - Krahn, Lois
AU - Todd, Michael
AU - Park, John G.
AU - St. Louis, Erik K.
AU - Morgenthaler, Timothy I.
AU - Hoffmann, Coles M.
AU - Hasanaj, Kristina
AU - Hollingshead, Kevin
AU - Yu, Tsung Yen
AU - Buman, Matthew P.
N1 - Publisher Copyright:
© 2023 Taylor & Francis Group, LLC.
PY - 2024
Y1 - 2024
N2 - Objective: To investigate the feasibility and acceptability of SleepWell24, a multicomponent, evidence-based smartphone application, to improve positive airway pressure therapy (PAP) adherence, among patients with obstructive sleep apnea (OSA) naive to PAP. Methods: In a single-blind randomized controlled trial, SleepWell24, with a companion activity monitor was compared to usual care plus the activity monitor and its associated app. SleepWell24 provides objective feedback on PAP usage and sleep/physical activity patterns, and chronic disease management. Patients were recruited from two sleep medicine centers and followed over the first 60 days of PAP. Feasibility and acceptability were measured by recruitment/retention rates, app usage, differences in post-trial Treatment Evaluation Questionnaire (TEQ) scores, and patient interviews. Exploratory, intent-to-treat logistic and linear mixed models estimated PAP adherence and clinical outcomes. Results: Of 103 eligible participants, 87 were enrolled (SleepWell24 n = 40, control n = 47; mean 57.6y [SD = 12.3], 44.8% female). Retention was ≥95% across arms. There were no significant differences in TEQ scores. SleepWell24 participants engaged with the app on 62.9% of trial days. PAP use was high across both arms (SleepWell24 vs. Control: mean hours 5.98 vs. 5.86). There were no differences in PAP adherence or clinical outcomes. Conclusions: SleepWell24 was feasible and acceptable among PAP-naive patients with OSA. Clinical Trial Registration: NCT03156283https://www.clinicaltrials.gov/study/NCT03156283.
AB - Objective: To investigate the feasibility and acceptability of SleepWell24, a multicomponent, evidence-based smartphone application, to improve positive airway pressure therapy (PAP) adherence, among patients with obstructive sleep apnea (OSA) naive to PAP. Methods: In a single-blind randomized controlled trial, SleepWell24, with a companion activity monitor was compared to usual care plus the activity monitor and its associated app. SleepWell24 provides objective feedback on PAP usage and sleep/physical activity patterns, and chronic disease management. Patients were recruited from two sleep medicine centers and followed over the first 60 days of PAP. Feasibility and acceptability were measured by recruitment/retention rates, app usage, differences in post-trial Treatment Evaluation Questionnaire (TEQ) scores, and patient interviews. Exploratory, intent-to-treat logistic and linear mixed models estimated PAP adherence and clinical outcomes. Results: Of 103 eligible participants, 87 were enrolled (SleepWell24 n = 40, control n = 47; mean 57.6y [SD = 12.3], 44.8% female). Retention was ≥95% across arms. There were no significant differences in TEQ scores. SleepWell24 participants engaged with the app on 62.9% of trial days. PAP use was high across both arms (SleepWell24 vs. Control: mean hours 5.98 vs. 5.86). There were no differences in PAP adherence or clinical outcomes. Conclusions: SleepWell24 was feasible and acceptable among PAP-naive patients with OSA. Clinical Trial Registration: NCT03156283https://www.clinicaltrials.gov/study/NCT03156283.
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U2 - 10.1080/15402002.2023.2289442
DO - 10.1080/15402002.2023.2289442
M3 - Article
C2 - 38032115
AN - SCOPUS:85178390280
SN - 1540-2002
VL - 22
SP - 420
EP - 432
JO - Behavioral Sleep Medicine
JF - Behavioral Sleep Medicine
IS - 4
ER -