[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100600731":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":27,"centralContacts":33,"locations":39,"responsibleParty":55,"collaborators":37,"id":58,"slug":59,"hasResults":60,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":64,"eligibilityCriteria":65,"healthyVolunteers":60,"sex":66,"minAge":67,"maxAge":37,"enrollmentInfo":68,"targetDuration":37,"studyType":71,"phases":72,"briefSummary":74,"conditions":75,"keywords":78,"overallStatus":41,"whyStopped":37,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},{"fullName":5,"class":6},"Memorial University of Newfoundland","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Immediate Treatment","EXPERIMENTAL","The immediate treatment group will begin the app-based insomnia intervention immediately after enrolling.",[13],"Behavioral: App-Based Cognitive Behavioural Therapy for Insomnia",{"label":15,"type":10,"description":16,"interventionNames":17},"Waitlist Control","The waitlist control group will begin the app-based intervention after a waiting period of 8 weeks after enrolling.",[13],[19],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":24},"BEHAVIORAL","App-Based Cognitive Behavioural Therapy for Insomnia","The iCANSleep app is based on an established CBT-I protocol. The core features of the iCANSleep app include 1) a modified CBT-I protocol for cancer survivors and 2) daily sleep diaries. Core components of CBT-I treatment to be implemented include sleep restriction, stimulus control, cognitive restructuring, and psychoeducation. These components will be modified into 7-weekly modules.",[9,15],[25,26],"Cognitive Behavioural Therapy for Insomnia","CBT-I",[28,31],{"name":29,"affiliation":5,"role":30},"Sheila N Garland","PRINCIPAL_INVESTIGATOR",{"name":32,"affiliation":5,"role":30},"Rachel M Lee",[34],{"name":29,"role":35,"phone":36,"phoneExt":37,"email":38},"CONTACT","1 (709) 864-8035",null,"icansleepapp@gmail.com",[40],{"facility":5,"status":41,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"RECRUITING","St. John's","Newfoundland and Labrador","A1B 3X9","Canada","CA",{"type":48,"coordinates":49},"Point",[50,51],-52.70931,47.56494,{"lat":51,"lon":50},[54],{"name":29,"role":35,"phone":36,"phoneExt":37,"email":38},{"type":30,"investigatorFullName":56,"investigatorTitle":57,"investigatorAffiliation":5,"oldNameTitle":37,"oldOrganization":37},"Sheila Garland","Associate Professor of Psychology and Oncology at Memorial University of Newfoundland","100600731","icansleep-smartphone-app-based-insomnia-treatment-for-cancer-survivors-100600731",false,"NCT07101302","iCANSleep: Smartphone App-Based Insomnia Treatment for Cancer Survivors","iCANSleep: A Randomized Controlled Trial of a Smartphone App-Based Insomnia Treatment for Cancer Survivors","iCANSleep","Inclusion Criteria:\n\n* Cancer survivors\n* Over 18 years of age\n* Lives in Canada\n* Understands English or French fluently\n* DSM-5 diagnosis of insomnia\n* ISI score of 8 or higher\n* Good performance status as indicated by a score of 0-2 on the Eastern Cooperative Oncology Group (ECOG) performance status scale\n* Access to internet connection\n* Ownership of smartphone\n* Fluency using mobile applications.\n* Individuals with non-hematological malignancies must show no evidence of cancer or clinically stable\u002Finactive 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.\n* 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 months prior.\n\nExclusion Criteria:\n\n* Presence of a sleep disorder other than insomnia that is not adequately treated (e.g., untreated sleep apnea)\n* Presence of a psychological disorder that is currently untreated or would impair the ability to participate (e.g., bipolar disorder)\n* Major sensory deficit (e.g., blindness)\n* Previous experience receiving CBT-I.\n* The use of medications prescribed for sleep (e.g., hypnotics, sedatives, or antidepressants) will be tracked and adjusted for in the statistical analysis.","ALL","18 Years",{"count":69,"type":70},146,"ESTIMATED","INTERVENTIONAL",[73],"NA","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.",[76,77],"Insomnia","Cancer",[79,76,80],"Cancer Survivor","Mobile Application","2026-02-18",{"date":83,"type":84},"2026-02-20","ACTUAL",{"date":86,"type":84},"2025-11-04",{"date":88,"type":70},"2026-11",{"name":5,"class":6},1]