Clinical Trials in China / NCT07357779
Recruiting
Not applicable
Clinical Efficacy and Health Economic Evaluation of an Intelligent Diagnostic and Treatment Model
NCT07357779 · tracked via the Priya Life Science China tracker
Condition(s) studied
Insomnia
Investigational drug(s) / intervention(s)
Intelligent Diagnostic and Treatment ModelTraditional treatment
Intelligent Diagnostic and Treatment Model: Intelligent CBTI
Traditional treatment: sleep drug treatment
Study summary
The purpose of this study is to evaluate the clinical and cost-effectiveness of an intelligent therapy based on digital cognitive behavioral therapy for insomnia disorders
Eligibility
Inclusion Criteria:
* (1) Clinical diagnosis of insomnia disorder; (2) Cooperate to complete the questionnaire surveys.
Exclusion Criteria:
* (1) Current use of central nervous system stimulants; (2) Use of analgesics, theophylline preparations, steroid medications; (3) Alcohol abuse or regular alcohol intake; (4) Diagnosis of other sleep disorders (e.g., obstructive sleep apnea, rapid eye movement sleep behavior disorder, restless legs syndrome) ; (5) Sleep disorders secondary to organic diseases (e.g., epilepsy, diabetes, renal failure).
Primary outcome measure(s)
- the score of Insomnia Severity Index scale — 6 weeks and 3 months
The total score ranges from 0 to 28, and a higher score indicates higher levels of insomnia severity. A score of 8 or greater is the cut point for clinically possible insomnia
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| the First Hospital of Jilin University | Changchun | Jilin | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07357779 on ClinicalTrials.gov ↗ ← All trials in China