{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["de Ruiter MHT"],"funding":["Fonds NutsOhra"],"pagination":["441-450"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5918490"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["22(2)"],"pubmed_abstract":["<h4>Purpose</h4>The Sleep Position Trainer (SPT) is a new option for treating patients with positional obstructive sleep apnea (POSA). This study investigated long-term efficacy, adherence, and quality of life during use of the SPT device compared with oral appliance therapy (OAT) in patients with POSA.<h4>Methods</h4>This prospective, multicenter trial randomized patients with mild to moderate POSA (apnea-hypopnea index [AHI] 5-30/h) to SPT or OAT. Polysomnography was performed at baseline and after 3 and 12 months' follow-up. The primary endpoint was OSA severity; adherence, quality of life, and adverse events were also assessed.<h4>Results</h4>Ninety-nine patients were randomized and 58 completed the study (29 in each group). Median AHI in the SPT group decreased from 13.2/h at baseline"],"journal":["Sleep & breathing = Schlaf & Atmung"],"pubmed_title":["Durability of treatment effects of the Sleep Position Trainer versus oral appliance therapy in positional OSA: 12-month follow-up of a randomized controlled trial."],"pmcid":["PMC5918490"],"funding_grant_id":["Project 1104-031"],"pubmed_authors":["de Lange J","de Ruiter MHT","de Vries N","Benoist LBL"],"additional_accession":[]},"is_claimable":false,"name":"Durability of treatment effects of the Sleep Position Trainer versus oral appliance therapy in positional OSA: 12-month follow-up of a randomized controlled trial.","description":"<h4>Purpose</h4>The Sleep Position Trainer (SPT) is a new option for treating patients with positional obstructive sleep apnea (POSA). This study investigated long-term efficacy, adherence, and quality of life during use of the SPT device compared with oral appliance therapy (OAT) in patients with POSA.<h4>Methods</h4>This prospective, multicenter trial randomized patients with mild to moderate POSA (apnea-hypopnea index [AHI] 5-30/h) to SPT or OAT. Polysomnography was performed at baseline and after 3 and 12 months' follow-up. The primary endpoint was OSA severity; adherence, quality of life, and adverse events were also assessed.<h4>Results</h4>Ninety-nine patients were randomized and 58 completed the study (29 in each group). Median AHI in the SPT group decreased from 13.2/h at baseline","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 May","modification":"2026-05-04T23:18:40.176Z","creation":"2019-03-26T23:34:24Z"},"accession":"S-EPMC5918490","cross_references":{"pubmed":["28913630"],"doi":["10.1007/s11325-017-1568-4"]}}