[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"WELT corp\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":72},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100615177","welt-rest-welt-randomized-evaluation-of-sleep-therapy-100615177",false,"NCT07289217","WELT-REST: WELT Randomized Evaluation of Sleep Therapy","A Randomized Controlled Decentralized Clinical Pilot Trial to Assess the Effectiveness and Sagety of the Digital Cognitive Behavioral Therapy Intervention SleepQ for Insomnia","WELT-REST","Inclusion Criteria:\n\n* Adult patients ≥18 years old\n* Confirmed current diagnosis of F51.0 Nonorganic insomnia or G47.0 Sleep disorders\n* Possession of a mobile device with internet connection (must be run on iOS software, minimum version 18) with internet connection\n* Sufficient German language proficiency required for the correct use of the intervention and the mobile device\n* Personal e-mail address for registration\n* Willing and able to provide written informed consent\n* Insomnia Severity Index (ISI) socre of 15 or higher, indicating clinically relevant symptoms of insomnia\n* Registered with a GP, sleep specialist or other health care professional\n\nExclusion Criteria:\n\n* Use of a digital interventioan for insomnia treatment in the past 6 months or planned use of comparable digital intervention during the study period\n* PHQ-9 score at screening ≥ 20 and\u002For item 9 f PHQ-9 ≥ 1\n* GAD-7 score at screening ≥ 15\n* Intermittent use and\u002For recent initiation (\\\u003C 3m) or planned use of insomnia specific prescription-only pharmacological therapy\n* Intermittent use and\u002For recent initiation (\\\u003C 3m) or planned use of a psychotropic during the study period which has recognised potential effects on insomnia\n* Participation in CBT or other psychotherapy to treat sleep disorders in the last 6 months (outpatient, inpatient) or planned start during the study period\n* Known history or diagnosis of substance or alchol abuse or dependence within 12 months prior to screening (diagnosis of F10-F19, excluding F17.1 and F17.2)\n* Current or planned participation in other clinical trials during the study period\n* Working in shifts\n* Currently pregnant or planning to become pregnant within the next 3 months\n* Any surgical procedure that was scheduled, planned, or conducted within the timeframe of the study (minor outpatient procedures under local anaesthetic or with no anesthetic are permitted)\n* Diagnosis of epilepsy\n* Presence of serious mental illness, such as (schizophrenia F 20.-, acute transient psychotic disorders F23.-, active manic episode F30.-, bipolar disorder F31.-, severe depression F32.3, F33.3)\n* Other diseases (such as acute or severe cardiac diseases, acute or severe respiratory diseases, acute or severe gastrointestinal diseases), conditions or therapies which, in the opinion of the investigator, could confound the study results or contraindicate participation.\n* Acute suicidal thoughts or intentions within the past 12 months\n* Presence of obstructive sleep apnea, restless legs syndrome, parasomnia, and other sleep behavior problem","ALL","18 Years",{"count":20,"type":21},80,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn whether the SleepQ mobile app can help reduce insomnia symptoms in adults diagnosed with insomnia. The main questions it aims to answer are:\n\n* Does adding the SleepQ app to care as usual (CAU) improve insomnia symptoms after 12 weeks?\n* Does SleepQ also improve depressive symptoms, anxiety, beliefs about sleep and daily functioning?\n\nResearchers will compare CAU + SleepQ to CAU alone to see whether SleepQ provides additional benefits for sleep and well-being.\n\nParticipants will take part remotely from home, be randomly assigned to either SleepQ+CAU or CAU alone, and complete online questionnaires at baseline, week 6, and week 12 about their sleep, mood, and daily functioning.\n\nParticipants in the intervention group will use the SleepQ app for 12 weeks while continuing their usual care.",[27],"Insomnia",[29,30,27,31,32,33,34],"dCBT - I","CBT - I","Cognitive Behavioral Therapy","Sleep Disorder","Digital Therapeutics","Digital CBT - I","NOT_YET_RECRUITING","2025-12-03",{"date":38,"type":39},"2025-12-17","ACTUAL",{"date":41,"type":21},"2025-12",{"date":43,"type":21},"2026-07",{"name":45,"class":46},"WELT corp","INDUSTRY",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},"100569496","digital-cbt-i-for-chronic-insomnia-100569496","NCT06695000","Digital CBT-I for Chronic Insomnia","A Multi-Site, Randomized, Wait-List Controlled Trial to Assess the Effectiveness and Safety of Digital Cognitive Behavioral Therapy for Insomnia (CBT-I) in Patients with Chronic Insomnia","Inclusion Criteria:\n\n* Meets diagnostic criteria for insomnia disorder according to the International Classification of Diseases, 10th Revision (ICD-10), including: F51: Nonorganic sleep disorders; G47: Sleep disorders\n* Has experienced insomnia symptoms for 3 months or longer.\n* Scores 8 or higher on the Insomnia Severity Index (ISI).\n* Oral and written fluency in Korean\n* Owns a smartphone and is independently able to use apps on a smartphone.\n* Voluntarily agrees to participate in this clinical study and provides signed informed consent.\n\nExclusion Criteria:\n\n* Currently receiving non-pharmacological treatments for insomnia (e.g., CBT-I, light therapy, traditional medicine for sleep) within the past 3 months from screening.\n* Diagnosed with other sleep disorders aside from insomnia and currently symptomatic, such as:\n\n  * Obstructive sleep apnea (G47.30)\n  * Sleep behavior disorders\n  * Restless leg syndrome (G28.8)\n  * Narcolepsy (G47.4)\n* Has an active, ongoing physical illness that impedes daily functioning, such as:\n\n  * Congestive heart failure\n  * Chronic obstructive pulmonary disease (COPD)\n  * Acute pain\n  * Neurological disorders (e.g., cerebrovascular disease)\n  * Neurodegenerative disorders (e.g., dementia, multiple sclerosis)\n  * Unstable medical conditions or life expectancy of less than 6 months\n* Adjustments in schedule or dosage of sleep medications, antidepressants, anticonvulsants, anxiolytics, or antipsychotics within the past 3 months, or use of PRN (as needed) prescribed sleep medications.\n* Engaged in shift work.\n* Pregnant individuals or those planning to become pregnant during the study period.\n* Any condition that the investigator believes would make participation in the study not in the best interest of the participant or would preclude successful completion of study activities","19 Years",{"count":57,"type":21},120,[24],"This study evaluates the effectiveness and safety of a digital Cognitive Behavioral Therapy program for Insomnia (CBT-I) in individuals with chronic insomnia. Participants will be randomly assigned to either begin digital CBT-I immediately or join a wait-list.",[61,62],"Insomnia Chronic","Insomnia Disorder","2024-11-15",{"date":65,"type":39},"2024-11-19",{"date":67,"type":21},"2025-01",{"date":69,"type":21},"2026-03",{"name":45,"class":46},5,""]