Chronic Insomnia
Conditions
Keywords
Digital cognitive behavior therapy for insomnia, Chronic Insomnia
Brief summary
The goal of this clinical trial is to explore whether cognitive behavioral intervention for insomnia(CBT-I) realized through audio, video, and articles on smartphone apps(ForSleep developed by the investigators) can improve the sleep quality of insomnia patients. The main question it aims to answer is: Does CBT-I delivered via smartphone apps improve sleep quality evaluated by scales in patients with insomnia? Investigators will compare the treatment group receiving the CBT-I intervention via smartphone apps to a control group receiving relaxation training to see if there are significant improvements in sleep quality. Participants will be asked to: Use an app(ForSleep) designed for CBT-I to follow a structured therapy program. Complete daily sleep diaries and periodic scales to track their sleep quality.
Detailed description
All participants sign the informed consent form online. The study is an online, single-blind, parallel-group, superiority randomized experiment of digital CBT-I(dCBT-I). The randomization is performed using stratified random sampling to ensure non-significant differences in age, gender, and basic sleep quality between the two groups. The screening, informed consent, assessments, allocation to conditions, delivery of the interventions, scale evaluations, and follow-ups are all carried out online. WeChat chatting groups for daily notification and communication are set up respectively. The experiment lasts 5 (and more) weeks included 3 weeks of intervention and 2 weeks of follow-up. All participants are required to keep sleep diaries. They self-evaluate via Insomnia Severity Index (ISI), Dysfunctional Beliefs and Attitudes about Sleep (DBAS), Sleep Hygiene Index (SHI), and Epworth Sleepiness Scale (ESS) to assess insomnia severity, sleep-related cognition, and behaviors at 5 time points. The first 3 times are at the first day, after 7 days and 14 days, before starting each new session. After 3-week program, the above scales are retaken during days 22\ 25 and days 36\ 39 as follow-ups. The evaluating time is different on account of individual rate of progress to accomplish the 3-week program. Digital cognitive behavioral therapy is delivered using an app developed by Fudan University. Digital intervention is structured into 3 sessions with a 7-days course in each session. The intervention group undertook 3 weeks of tasks which consisted of cognitive, behavioral, and relaxation parts of CBT-I and typically lasted 15 minutes per day. Two pieces of relaxing music are recommended daily to the control group instead of the standard relaxation practice. All participants have access to 30 relaxing music and articles on sleep hygiene that are made available in the app.
Interventions
BEHAVIORALdCBT-I
A digital cognitive behavioral intervention course that addresses multiple aspects such as basic sleep knowledge, sleep hygiene, sleep behaviors, improving negative cognition, and improving emotions. The intervention is delivered through video, audio, and text formats.
BEHAVIORALRelaxing music
Participants can freely listen relaxing music
Sponsors
Jia Xiu
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* Age 18-65 years old * Insomnia Severity Index Scale (ISI) score of 8\ 21 * Proficient in the use of smartphones * Chinese native speaker
Exclusion criteria
* Those with other combined sleep problems, such as apnoea syndrome, restless leg syndrome, etc. * Women during pregnancy * risky jobs that require high concentration, such as working at heights, long-distance driving, etc. * previous or current diagnosis of severe neurological disorders such as epilepsy * previous or current diagnosis of mental illness such as depression, bipolar disorder, schizophrenia, obsessive-compulsive disorder, etc. * history of drug or alcohol abuse * a significant negative risk of suicide * serious physical illness (e.g., cardiovascular, hepatic, renal, etc.)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pittsburgh Sleep Quality Index Scale(PSQI) | baseline(before the intervention); intervention stage(every week during 3-week intervention); follow-up stage(every week during 2-week follow-up) | A scale that evaluates sleep quality, the scale scores range from 0 to 21, and lower scores mean a better outcome |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Dysfunctional Beliefs and Attitudes about Sleep Scale(DBAS) | baseline(before the intervention); intervention stage(every week during 3-week intervention); follow-up stage(every week during 2-week follow-up) | A scale that evaluates the sleep attitude, the scale scores range from 0 to 64, and lower scores mean a better outcome |
| Sleep Hygiene Index Scale(SHI) | baseline(before the intervention); intervention stage(every week during 3-week intervention); follow-up stage(every week during 2-week follow-up) | A scale that evaluates sleep hygiene, the scale scores range from 0 to 52, and lower scores mean a better outcome |
| The Insomnia Severity Index Scale(ISI) | baseline(before the intervention); intervention stage(every week during 3-week intervention); follow-up stage(every week during 2-week follow-up) | A scale that evaluates the severity of insomnia, the scale scores range from 0 to 28, and lower scores mean a better outcome |
| Epworth Sleepiness Scale(ESS) | baseline(before the intervention); intervention stage(every week during 3-week intervention); follow-up stage(every week during 2-week follow-up) | A scale that evaluates sleepiness, the scale scores range from 0 to 24, and lower scores mean a better outcome |
Countries
China
Outcome results
None listed