针对同时存在的夜尿症和慢性失眠症的认知行为综合疗法的多点可行性研究。

Constance H Fung, Alison J Huang, Alayne D Markland, Michael Schembri, Jennifer L Martin, Donald L Bliwise, Jing Cheng, Cathy A Alessi, Theodore M Johnson, Kathryn L Burgio, Lisa Muirhead, Alison Neymark, Erin Der-Mcleod, Taressa Sergent, Ann Chang, Scott R Bauer, Colette Spencer, Andrew Guzman, Camille P Vaughan
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引用次数: 0

摘要

背景:老年人夜尿(夜间从睡眠中醒来排尿)和慢性失眠经常并存,共同导致睡眠障碍。治疗通常只针对夜尿或失眠,而不是同时解决这些疾病的共同机制:我们进行了一项多地点可行性研究,目的是(方法:我们进行了一项多地点可行性研究:(1)测试并完善了针对同时患有夜尿症和失眠症的老年人的招募、随机化和评估方案;(2)检查了结果测量的初步变化,为未来更大规模的多地点临床试验提供参考。参与者是从门诊诊所招募的 60 岁及以上的男性和女性,在过去 4 周内平均每晚有两次或两次以上的夜尿症发作,并符合慢性失眠症的诊断标准。参与者被随机分配接受失眠和夜尿症的综合认知行为疗法或健康教育对照项目,其中健康教育对照项目包括每周五次由训练有素的执业护士干预人员进行的访问。结果(如夜尿次数)在治疗后一周和随机后四个月进行测量。描述性统计分析了结果的可行性,以指导未来疗效试验的准备工作:在筛选出的 245 名成人中,55% 不符合条件,25% 拒绝参与。在提供知情同意书的 49 名参与者中,61% 接受了随机治疗。在随机抽取的 30 名参与者(平均年龄 70.6 岁,60% 为白人)中,14 人被分配到认知行为综合治疗组,16 人被分配到对照组。所有随机参与者都提供了 4 个月的随访数据。4个月后,与基线相比,综合治疗组的平均夜尿次数减少了0.9次(标准差为1.0次),对照组的平均夜尿次数减少了0.2次(标准差为1.2次):讨论:研究结果表明,从老年人(主要为男性)中招募、随机分配并收集结果数据是可行的,这些老年人被分配到治疗同时存在的失眠和夜尿症的认知行为综合疗法或健康教育对照项目中。
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A multisite feasibility study of integrated cognitive-behavioral treatment for co-existing nocturia and chronic insomnia.

Background: Nocturia (waking from sleep at night to void) and chronic insomnia frequently co-exist in older adults, contributing synergistically to sleep disturbance. Treatments typically target either nocturia or insomnia rather than simultaneously addressing shared mechanisms for these disorders.

Methods: We conducted a multisite feasibility study to: (1) test and refine a protocol for recruitment, randomization, and assessment of older adults with co-existing nocturia and insomnia; and (2) examine preliminary changes in outcome measures to inform a future larger, multisite clinical trial. Participants were men and women aged 60 years and older recruited from outpatient clinics, reporting an average of two or more nocturia episodes per night over the past 4 weeks and meeting diagnostic criteria for chronic insomnia disorder. Participants were randomized to receive either integrated cognitive-behavioral therapy for insomnia and nocturia or a health education control program involving five weekly visits with a trained nurse practitioner interventionist. Outcomes (e.g., nocturia episodes) were measured 1-week post-treatment and 4-month post-randomization. Descriptive statistics examined the feasibility of outcomes to guide preparations for a future efficacy trial.

Results: Of 245 adults screened, 55% were ineligible and 25% declined to participate. Sixty-one percent of 49 participants who provided informed consent were randomized. Of the 30 participants randomized (mean age = 70.6 years, 60% White), 14 were assigned to integrated cognitive-behavioral treatment and 16 to the control group. All randomized participants provided 4-month follow-up data. At 4 months, mean nightly nocturia episodes decreased by 0.9 (SD 1.0) in the integrated treatment group and by 0.2 (SD 1.2) in the control group compared with baseline.

Discussion: Findings demonstrate the feasibility of recruiting, randomizing, and collecting outcome data from older adults (predominantly male) assigned to an integrated cognitive-behavioral therapy for coexisting insomnia and nocturia or a health education control program.

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