Intervention Design and Trial Protocol: Mindfulness-based Exposure for PAP-associated Claustrophobia

被引:2
作者
Gawrysiak, Michael J. [1 ,2 ]
Baime, Michael [2 ]
King, Tonya S. [3 ]
Watach, Alexa J. [4 ]
McPhillips, Miranda, V [4 ,5 ]
Kolanowski, Ann [6 ]
Schutte-Rodin, Sharon [2 ]
Sawyer, Amy M. [4 ,5 ,7 ]
机构
[1] West Chester Univ Penn, Dept Psychol, W Chester, PA USA
[2] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Penn State Coll Med, Dept Publ Hlth Sci, Hershey, PA USA
[4] Univ Penn, Ctr Sleep & Circadian Neurobiol, Philadelphia, PA 19104 USA
[5] Univ Penn, Sch Nursing, Philadelphia, PA 19104 USA
[6] Penn State Univ, Coll Nursing, University Pk, PA 16802 USA
[7] Corporal Michael J Crescenz Vet Affairs Med Ctr, Philadelphia, PA USA
关键词
mindfulness; obstructive sleep apnea (OSA); positive airway pressure (PAP); claustrophobia; exposure therapy; treatment adherence; POSITIVE AIRWAY PRESSURE; OBSTRUCTIVE SLEEP-APNEA; INSOMNIA SEVERITY INDEX; ADHERENCE; THERAPY; ANXIETY; DEPRESSION; NONADHERENCE; ACCEPTANCE; INVENTORY;
D O I
10.1177/0193945920924608
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
Positive airway pressure (PAP) associated claustrophobia is common among obstructive sleep apnea patients and plays a prominent role in low adherence and treatment failure. As there are no evidence-based interventions for PAP-associated claustrophobia, the objective of the present research is to pilot test Mindfulness-based Exposure for PAP-associated Claustrophobia, in sleep apnea adults that present with treatment non-adherence and claustrophobia. This approach combines Mindfulness-based Stress Reduction with exposure-based treatment components to target this treatment-associated claustrophobia. The present article outlines the mindfulness exposure intervention design and methods and reports the pilot trial study protocol. Trial findings are intended to: (a) develop a preliminary effect size of the intervention on PAP-associated claustrophobia; (b) explore differences in treatment adherence by group (intervention vs control); and (c) establish feasibility for expanded protocol implementation, delivery, and participant acceptability of the intervention to support subsequent design of a fully powered randomized controlled trial.
引用
收藏
页码:261 / 272
页数:12
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