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Completed

NCT Number: NCT06481423

Digital Management of Sleep Health

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University

Shanghai, Shanghai Municipality, 200433, China

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.)

Treatment and study plan

dCBT-I

Behavioral

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.

Relaxing music

Behavioral

Participants can freely listen relaxing music

Primary outcomes

  1. Pittsburgh Sleep Quality Index Scale(PSQI)

    Time frame: 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 outcomes

  1. Dysfunctional Beliefs and Attitudes about Sleep Scale(DBAS)

    Time frame: 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

  2. Sleep Hygiene Index Scale(SHI)

    Time frame: 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

  3. The Insomnia Severity Index Scale(ISI)

    Time frame: 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

  4. Epworth Sleepiness Scale(ESS)

    Time frame: 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

Sponsors and collaborators

Lead sponsor

Jia Xiu

Other

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Jul 1, 2024
Registry last updated
Jun 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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