← Back to Clinical Trials
Recruiting NCT07101302

iCANSleep: Smartphone App-Based Insomnia Treatment for Cancer Survivors

Trial Parameters

Condition Insomnia
Sponsor Memorial University of Newfoundland
Study Type INTERVENTIONAL
Phase N/A
Enrollment 146
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-11-04
Completion 2026-11
All Conditions
Interventions
App-Based Cognitive Behavioural Therapy for Insomnia

Brief Summary

The investigators will answer the question of whether treating insomnia using the mobile-app-based intervention of Cognitive Behavioural Therapy for Insomnia (CBT-I) for cancer survivors ("iCANSleep") can improve symptoms of insomnia in Canadian cancer survivors compared to a waitlist control group. The investigators will recruit 146 people with insomnia who have completed cancer treatment at least 3 months prior to the study.

Eligibility Criteria

Inclusion Criteria: * Cancer survivors * Over 18 years of age * Lives in Canada * Understands English or French fluently * DSM-5 diagnosis of insomnia * ISI score of 8 or higher * Good performance status as indicated by a score of 0-2 on the Eastern Cooperative Oncology Group (ECOG) performance status scale * Access to internet connection * Ownership of smartphone * Fluency using mobile applications. * Individuals with non-hematological malignancies must show no evidence of cancer or clinically stable/inactive disease for a minimum of 3 months prior to enrollment (for individuals with non-metastatic cancer) or be on a stable treatment regimen for the prior 3 months (for individuals with metastatic cancer) to ensure that insomnia is not a direct, acute response to cancer treatment. * Individuals with hematological malignancies must be in remission at the time of recruitment and have completed cancer treatments (e.g., transplant, chemotherapy, immunotherapy, radiotherapy) at least 3 mont

Related Trials