A Randomised Controlled Trial of the Effects of Cognitive Behavioural Therapy and Bright Light Therapy for Insomnia in Adolescents With Evening Chronotype

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Insomnia is prevalent in adolescents. Together with an increase of evening preference (i.e. evening chronotype) in adolescent, sleep disturbance in adolescents are associated with a constellation of adverse outcomes. Insomnia and evening chronotype in adolescents are also found to predict the development of mental health problems and negative health-related outcomes in young adulthood. While cognitive behavioural therapy for insomnia (CBT-I) and bright light therapy were evidenced to be effective in managing sleep problems in adults, there is limited evidence to support their efficacy in children and adolescents. To address the limitations in the existing literature, this study aims to conduct a randomised controlled trial to examine the effects of CBT-I and light therapy on insomnia and mood symptoms, and other clinical and daytime symptoms, as well as overall functioning in adolescents with insomnia (particularly sleep onset insomnia) and evening chronotype.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Maximum Age: 24
Healthy Volunteers: f
View:

• Chinese aged 12-24 years old;

• Predominant complaint of difficulty in initiating sleep at least three times a week and for at least 3 months;

• Show clinically significant impairment / distress;

• Having a score of \>= 9 on the Insomnia Severity Index (ISI) ;

• Classified as evening chronotype based on the score of reduced Horne-Östberg Morning-Eveningness Questionnaire (rMEQ; i.e. \<12) and having a sleep onset time of 11:15pm or later for 12 year olds, 11:30pm or later for 13-14 year olds, and 12:00am or later for 15 years or above at least 3 nights per week for the past 3 month as confirmed by a 7-day sleep diary;

• Written informed consent of participation into the study is given by the participant and his/her parent or guardian (for those aged under 18);

• Being able to comply with the study protocol.

Locations
Other Locations
Hong Kong Special Administrative Region
Sleep Research Clinic and Laboratory, Department of Psychology, The University of Hong Kong
RECRUITING
Hong Kong
Contact Information
Primary
Shirley X Li, DClinPsy
shirley.li@hku.hk
39177035
Time Frame
Start Date: 2023-03-01
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 150
Treatments
Experimental: CBT-I + Bright Light
n = 50
Active_comparator: CBT-I + Placebo Light
n = 50
No_intervention: Wait-list Control
n = 50
Related Therapeutic Areas
Sponsors
Collaborators: Chinese University of Hong Kong, Flinders University, University of Oxford
Leads: The University of Hong Kong

This content was sourced from clinicaltrials.gov