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Intervention for Chronic Insufficient Sleep in Young Adult Cancer Patients and Survivors

StatusNot Yet Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 3 months later Sep 30, 2027 → Dec 31, 2027
See other at-risk trials from Medstar Health Research Institute

Record History

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  1. Start date: Sep 1, 2026 to Jan 4, 2027
    • Primary completion pushed from Sep 30, 2027 to Dec 31, 2027
    • Eligibility criteria expanded, about 9 words
    • Secondary endpoints: details revised at 5 of 5 entries
  2. Start date: Jan 1, 2026 to Sep 1, 2026
    • Primary completion moved earlier from May 31, 2028 to Sep 30, 2027
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Young adult cancer survivors (YACS) commonly experience chronic insomnia due to many factors such as cancer related symptoms, effects of anti-cancer therapies, co-morbid mood disorders, and/or other psychosocial and economic stressors. Cognitive behavioral therapy for insomnia (CBT-I) is the gold standard for insomnia management but remains challenging to deliver to patients due to limited numbers of trained therapists, inconvenient scheduling availability, or prohibitive therapy costs. To address this critical gap in young adult cancer survivorship, the investigators propose to develop and test efficacy of the More Sleep Hours Electronic Education Program (More SHEEP), a novel system of smart speaker, smart lighting, and specialized Wi-Fi router that delivers AI-driven CBT-I to patients at home.
Trial Details
NCT Number NCT07318545
Lead Sponsor Medstar Health Research Institute
Collaborators: National Cancer Institute (NCI)
Conditions
(from sponsor)		 Cancer
Related terms Neoplasms
Enrollment 74 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov