The effect of group-based cognitive behavioural therapy for insomnia in patients with rheumatoid arthritis: a randomized controlled trial

医学 随机对照试验 物理疗法 失眠症 多导睡眠图 人口 认知行为疗法 内科学 精神科 呼吸暂停 环境卫生
作者
K. M. Latocha,Katrine Løppenthin,Mikkel Østergaard,Poul Jennum,Merete Lund Hetland,Henrik Røgind,Tine Lundbak,Julie Midtgaard,Robin Christensen,Bente Appel Esbensen
出处
期刊:Rheumatology [Oxford University Press]
卷期号:62 (3): 1097-1107 被引量:12
标识
DOI:10.1093/rheumatology/keac448
摘要

Abstract Objectives The primary objective was to compare the effect of cognitive behavioural therapy for insomnia (CBT-I) to usual care on sleep efficiency, measured by polysomnography (PSG) immediately after the intervention at week 7. Secondary objectives included comparing the longer-term effect on sleep- and RA-related outcomes at week 26. Methods In a randomized controlled trial using a parallel group design, the experimental intervention was 6 weeks’ nurse-led group-based CBT-I; the comparator was usual care. Analyses were based on the intention-to-treat (ITT) principle; missing data were statistically modelled using repeated-measures linear mixed effects models adjusted for the level at baseline. Results The ITT population consisted of 62 patients (89% women), with an average age of 58 years and an average sleep efficiency of 83.1%. At primary end point, sleep efficiency was 88.7% in the CBT-I group, compared with 83.7% in the control group (difference: 5.03 [95% CI −0.37, 10.43]; P = 0.068) measured by PSG at week 7. Key secondary outcomes measured with PSG had not improved at week 26. However, for all the patient-reported key secondary sleep- and RA-related outcomes, there were statistically highly significant differences between CBT-I and usual care (P < 0.0001), e.g. insomnia (Insomnia Severity Index: −9.85 [95% CI −11.77, −7.92]) and the RA impact of disease (RAID: −1.36 [95% CI −1.92, −0.80]) at week 26. Conclusion Nurse-led group-based CBT-I did not lead to an effect on sleep efficiency objectively measured with PSG. However, CBT-I showed improvement on all patient-reported key secondary sleep- and RA-related outcomes measured at week 26. Trial registration ClinicalTrials.gov, https://clinicaltrials.gov, NCT03766100.
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