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Innovating CBT-I for cancer survivors: study protocol for a randomized controlled optimization trial

Title: Innovating CBT-I for cancer survivors: study protocol for a randomized controlled optimization trial
Authors: Balkind, Emma G.; Willis, Kelcie D.; Bolden, Caleb; Muzikansky, Alona; Gorman, Mark J.; Comander, Amy H.; Haggett, Dana; Wagner, Lynne; Kossowsky, Joe; Park, Elyse R.; Mukhammadov, Timur; Adewumi, Tolulope; L. Hall, Daniel
Source: International Journal of Clinical Trials; Vol. 12 No. 2 (2025): April-June 2025; 127-135 ; 2349-3259 ; 2349-3240
Publisher Information: Medip Academy
Publication Year: 2025
Subject Terms: Insomnia; CBT-I; Survivorship; Cancer; Oncology; Optimization; MOST
Description: Background: Insomnia is a significant issue in 30-50% of cancer survivors. Our pilot randomized controlled trial of synchronous, virtual cognitive behavioral therapy for insomnia (CBT-I) for cancer survivors suggested that a group format or booster sessions may optimize effects on insomnia and daytime functioning. The goal of this project is to conduct a factorial, randomized controlled trial to optimize synchronous, virtual delivery of CBT-I for cancer survivors. Methods: We will conduct a 2×2 factorial trial (N=80) to evaluate the optimal combination of two intervention design components: delivery (individual vs. group) and booster sessions (0 vs 3). The primary outcome is change in insomnia severity (insomnia severity index) from T0 (week 0) to T2 (week 8). The secondary outcomes are acute (T0-T1, week 4) and sustained (T0-T3, week 16) changes in insomnia severity, emotional distress, work-related functioning, use of sleep medications, and subjective and objective sleep metrics (measured with sleep diaries and Fitbit). Exploratory aim 1 is to characterize study participation and sleep outcomes among racial and ethnic minority cancer survivors with insomnia. Exploratory aim 2 is to characterize the acceptability of design components using Likert ratings (very low=1 to very high=5, benchmarks=4 or higher) and exit interviews with open-ended responses with probes. Conclusions: This project will yield multiple deliverables to innovate cancer survivorship care, chiefly an optimized, scalable, virtually delivered intervention that addresses chronic insomnia, one of the most deleterious concerns among the among the steadily increasing number of cancer survivors. Trial Registration: NCT06181643.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
Relation: https://www.ijclinicaltrials.com/index.php/ijct/article/view/863/472; https://www.ijclinicaltrials.com/index.php/ijct/article/view/863
DOI: 10.18203/2349-3259.ijct20251208
Availability: https://www.ijclinicaltrials.com/index.php/ijct/article/view/863; https://doi.org/10.18203/2349-3259.ijct20251208
Rights: Copyright (c) 2025 International Journal of Clinical Trials
Accession Number: edsbas.FA9265D8
Database: BASE