No pain, no gain: An exploratory within-subjects mixed-methods evaluation of the patient experience of sleep restriction therapy (SRT) for insomnia

被引:135
|
作者
Kyle, Simon D. [1 ,2 ]
Morgan, Kevin [3 ]
Spiegelhalder, Kai [4 ]
Espie, Colin A. [1 ,2 ]
机构
[1] Univ Glasgow, Sleep Ctr, Sackler Inst Psychobiol Res, Glasgow G51 4TF, Lanark, Scotland
[2] Univ Glasgow, Inst Neurosci & Psychol, Coll Med Vet & Life Sci, Glasgow G51 4TF, Lanark, Scotland
[3] Univ Loughborough, Clin Sleep Disorders Unit, Loughborough, Leics, England
[4] Univ Freiburg, Med Ctr, Dept Psychiat & Psychotherapy, D-7800 Freiburg, Germany
关键词
Insomnia; Treatment; Patient experience; Qualitative; Side-effects; COGNITIVE-BEHAVIORAL THERAPY; MEDICINE; MODAFINIL; FATIGUE; TRIAL; LIFE; CBT;
D O I
10.1016/j.sleep.2011.03.016
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To explore the patient experience of Sleep Restriction Therapy (SRT) for insomnia, with particular focus on elucidating possible side-effects, challenges to adherence and implementation and perceptions of benefit/impact. Methods: To fully investigate the patient experience of sleep restriction therapy for insomnia we designed a within-subjects mixed-method study, employing sleep and daytime functioning questionnaires, assessments of sleep-restriction-related side-effects, prospective qualitative audio-diaries and post-treatment semi-structured interviews. University of Glasgow Sleep Centre. Eighteen patients with Primary Insomnia (mean age = 42; range 18-64). Patients took part in a 4-week brief sleep restriction intervention, involving two group sessions and two subsequent follow-up phone calls in the home environment. Measurements and results: Sleep diaries and global measures of insomnia severity and sleep quality, as expected, demonstrated robust improvements at both post-treatment and 3-month follow-up (all large effect sizes). Daytime functioning/health-related quality of life variables similarly evidenced strong treatment effects (moderate to large effect sizes). Reported side-effects were common, with >= 50% of patients reporting impairment in 8 out of 12 listed symptoms as a consequence of initiating treatment. The four most common side-effects were 'fatigue/exhaustion' (100%), 'extreme sleepiness' (94%), 'reduced motivation/energy' (89%) and 'headache/migraine' (72%) [Mean number of symptoms per patient = 7.2 (2.4); range 3-11]. Intriguingly, both side-effect frequency and ratings of side-effect interference were associated with baseline to post-treatment improvements in sleep quality. Qualitative real-time audio-diaries during week 1 of treatment and post-treatment interviews provided rich accounts of side-effects associated with acute SRT implementation: general challenges surrounding treatment implementation and adherence/non-adherence; and modifications to sleep parameters, daytime functioning and perceptions of sleep/sleep period. Conclusions: This work has important implications for the delivery of SRT, particularly concerning awareness of possible 'adverse events' and likely implementation/adherence challenges. Findings also pave the way for testable hypotheses concerning possible mechanisms of action involved in sleep restriction treatment. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:735 / 747
页数:13
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