Skip to content

E-aid Cognitive Behavioral Therapy for Insomnia Disorder to Prevent Acute Insomnia from becoming Chornic : A Randomized Controlled Trial

E-aid Cognitive Behavioral Therapy for Insomnia Disorder to Prevent Acute Insomnia from becoming Chornic : A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066448
Enrollment
Unknown
Registered
2022-12-06
Start date
2022-12-15
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Insomnia disorder

Interventions

Treatment group :E-aid Cognitive Behavior Therapy
Control group :E-aid Sleep Hygiene Education I

Sponsors

Nanfang Hospital, Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: A.meeting the criteria of brief insomnia disorder according to the 5th edition of the Diagnostic and Statistical Manual of Mental Disorders (DMS-5); B.patients with stable physical diseases, psychiatric disorders, and sleep disorders, including those taking medication (e.g., blood pressure medications, antidepressants, benzodiazepines, etc.), were allowed to continue with their current treatment regimen (Treat As Usual, TAU) but did not change the type or dose of medication during the first 2 weeks of enrollment; C.18 to 60 years old; D.the study protocol can be understood and followed; E.written informed consent can be provided online; F.have and know how to use smart terminals (e.g. smartphones, tablets, computers, etc.).

Exclusion criteria

Exclusion criteria: A. a current diagnosis of any other uncured physical diseases, mental disorders or sleep disorders ; B. current psychological treatment with insomnia disorder; C. rotating shift-work, night work or frequent cross-time zone fliers (e.g.international flight crew); polysomnography(PSG) revealed sleep apnea syndrome (Apnea-Hypopnea Index [AHI] >= 15 beats/hour) or periodic limb movement disorder (Periodic Limb Movement Index [PLMI] >= 15 times/hour). E. pregnant or lactating women; F. other circumstances not suitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Incidence of chronic insomnia;Polysomnography, PSG;

Secondary

MeasureTime frame
Insomnia Severity Index;Ford Insomnia Response to Stress Test;Dysfunctional Beliefs and Attitudes on Sleep-16 items;Sleep Hygiene and Practices Scale;Glasgow Sleep Effort Scale;Dysfunctional Beliefs and Attitudes on Sleep - 16 items;Morning and Evening Questionnaire -5 items;Epworth Sleepiness Scale;PHQ-9;General Anxiety Disorder-7;sleep dairy;Self-administered economic cost questionnaire;Work Productivity And Activity Impairment Questionnaire , WPAI;Five-level version of the EuroQol five-dimensional, EQ-5D-5L;ActiGraph;gut microbes;hair;hair;Blood;General demographic questionnaire;Pre-sleep Arousal Scale;

Countries

China

Contacts

Public ContactBin Zhang

Nanfang Hospital, Southern Medical University

zhang73bin@hotmail.com+86 13527807502

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026