Skip to main content
Clinical Trials/NCT04806009
NCT04806009
Unknown
Not Applicable

Evaluating an Online Mindfulness-Based Intervention for Individuals With Insomnia in China: A Randomized Controlled Trial

Central South University0 sites1,000 target enrollmentJanuary 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Insomnia, Primary
Sponsor
Central South University
Enrollment
1000
Primary Endpoint
change of sleep quality
Last Updated
5 years ago

Overview

Brief Summary

Insomnia has significantly negative impact on work, quality of life, psycho-somatic health on individuals and imposes substantial economic burdens on society. Mindfulness-based interventions (MBIs) have shown its efficacy in the treatment of insomnia, however the effect of online MBIs need more studies to verify. This study aims to compare the effectiveness of an online MBI named 'Mindful Living With Insomnia (MLWI)' to online CBI-I for insomnia.

Detailed Description

This will be an online based, randomized, controlled trial. Investigators will recruit 1000 participants, and will randomize and allocate participants 1:1 to the 'Mindful Living With Insomnia (MLWI)' group (n=500) and the 'CBT-I' group (n=500). The Intervention will involve 12 sessions over 6 weeks course, 2 sessions a week and 0.5 hours per session. The primary outcome will be sleep quality assessed by the Pittsburgh Sleep Quality Index (PSQI), severity of insomnia symptoms assessed by the Insomnia Severity Index (ISI), and sleep parameters recorded using Mi Smart Band. The secondary outcomes include perceived stress, anxiety, depression, and mindfulness. Outcomes will be evaluated at baseline, the end of the intervention period, and at a 3-month follow-up. Analysis of covariance, regression analysis, χ2 test, t-test, Pearson's correlations will be applied in data analysis.

Registry
clinicaltrials.gov
Start Date
January 1, 2022
End Date
March 31, 2023
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Central South University
Responsible Party
Principal Investigator
Principal Investigator

Chen Pan

Principal Investigator

Central South University

Eligibility Criteria

Inclusion Criteria

  • Age between 18 and 59 years old
  • Being able to read and write Chinese
  • PSQI exceeding 5 at screening
  • Being able to access online services
  • Willing to participate in the study

Exclusion Criteria

  • Unable to communicate
  • With somatic disorders
  • With mental disorders except for insomnia disorder
  • Being treated with pharmacotherapy
  • Significant current mindfulness practices (\>15 minutes/ day)

Outcomes

Primary Outcomes

change of sleep quality

Time Frame: Outcomes will be evaluated at baseline, the end of the 6-week Intervention Period, and at a 3-month follow-up

The 19-item Pittsburgh Sleep Quality Index (PSQI) measured sleep quality subjectively and assesses sleep disturbances during the past month on a 4-point Likert scale of 0 -3.A lower global PSQI score indicates better sleep quality.

Secondary Outcomes

  • change of severity of insomnia symptoms(Outcomes will be evaluated at baseline, the end of the 6-week Intervention Period, and at a 3-month follow-up)
  • change of perceived stress(Outcomes will be evaluated at baseline, the end of the 6-week Intervention Period, and at a 3-month follow-up)
  • change of mindfulness(Outcomes will be evaluated at baseline, the end of the 6-week Intervention Period, and at a 3-month follow-up)
  • change of sleep duration and quality(Outcomes will be evaluated at baseline, the end of the 6-week Intervention Period, and at a 3-month follow-up)
  • change of depression(Outcomes will be evaluated at baseline, the end of the 6-week Intervention Period, and at a 3-month follow-up)
  • change of anxiety(Outcomes will be evaluated at baseline, the end of the 6-week Intervention Period, and at a 3-month follow-up)

Similar Trials