Journal
CANCER
Volume 128, Issue 7, Pages 1532-1544Publisher
WILEY
DOI: 10.1002/cncr.34066
Keywords
cancer; insomnia; randomized controlled trial; survivorship; virtual interventions
Categories
Funding
- American Cancer Society (Massachusetts General Hospital Institutional Research Grant)
- National Center for Complementary and Integrative Health [K23AT010157]
- National Cancer Institute [K24CA197382]
- National Heart, Lung, and Blood Institute Research Training Program in Sleep, Circadian, and Respiratory Neurobiology through the Division of Sleep Medicine at Harvard Medical School and Brigham and Women's Hospital [T32HL007901]
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The study adapted and assessed the feasibility, acceptability, and preliminary effects of synchronous, virtual CBT-I for cancer survivors. The Survivorship Sleep Program (SSP) showed large, clinically significant improvements in insomnia severity and positive effects on other sleep metrics, suggesting its efficacy in reducing insomnia severity among cancer survivors.
Background For cancer survivors, insomnia is prevalent, distressing, and persists for years if unmanaged. Cognitive behavioral therapy for insomnia (CBT-I) is an effective treatment yet can be difficult to access and may require modification to address survivorship-specific barriers to sleep. In this 2-phase study, the authors adapted and assessed the feasibility, acceptability, and preliminary effects of synchronous, virtual CBT-I adapted for cancer survivors (the Survivorship Sleep Program [SSP]). Methods From April to August 2020, cancer survivors with insomnia (N = 10) were interviewed to refine SSP content and delivery. From October 2020 to March 2021, 40 survivors were recruited for a randomized controlled trial comparing 4 weekly SSP sessions with enhanced usual care (EUC) (CBT-I referral plus a sleep hygiene handout). Feasibility and acceptability were assessed by enrollment, retention, attendance, fidelity, survey ratings, and exit interviews. Insomnia severity (secondary outcome), sleep quality, sleep diaries, and fatigue were assessed at baseline, postintervention, and at 1-month follow-up using linear mixed models. Results The SSP included targeted content and clinician-led, virtual delivery to enhance patient centeredness and access. Benchmarks were met for enrollment (56% enrolled/eligible), retention (SSP, 90%; EUC, 95%), attendance (100%), and fidelity (95%). Compared with EUC, the SSP resulted in large, clinically significant improvements in insomnia severity (Cohen d = 1.19) that were sustained at 1-month follow-up (Cohen d = 1.27). Improvements were observed for all other sleep metrics except sleep diary total sleep time and fatigue. Conclusions Synchronous, virtually delivered CBT-I targeted to cancer survivors is feasible, acceptable, and seems to be efficacious for reducing insomnia severity. Further testing in larger and more diverse samples is warranted.
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