Efficacy of Cognitive Behavioural Therapy for Insomnia and Bright Light Therapy in Adolescents With ADHD and Comorbid Insomnia and Evening Chronotype: A Randomised, Assessor Blind, Parallel-group Trial
Efficacy of Cognitive Behavioural Therapy for Insomnia and Bright Light Therapy in Adolescents With ADHD and Comorbid Insomnia and Evening Chronotype: A Randomised, Assessor Blind, Parallel-group Trial
Attention-deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder characterised by persistent inattention, hyperactivity, and impulsivity. In adolescents and young people, ADHD is commonly accompanied by insomnia and circadian delay. These co-occurring sleep and circadian disturbances may negatively affect daytime functioning and overall clinical outcomes. Although cognitive behavioural therapy for insomnia (CBT-I) is considered the first-line treatment for insomnia, and bright light therapy may help address circadian issues, their efficacy in adolescents with ADHD and comorbid insomnia and eveningness remains unexplored. This study aims to evaluate whether CBT-I, with or without bright light therapy, improves insomnia, sleep, and circadian as well as other clinical outcomes, and cognitive functioning in youths with ADHD and whether these interventions can also lead to improvements in mood and other clinical symptoms, as well as cognitive functioning.
Inclusion criteria:
An adolescent who meets the following criteria will be eligible for taking part in this study:
Exclusion criteria:
An adolescent who meets one or more of the following criteria will be excluded from the study:
shirley.li@hku.hk39177035
An assessor-blind, three-arm, parallel-group, randomised controlled trial will be conducted in youths with ADHD, comorbid insomnia, and evening chronotype. Eligible participants will be randomised to one of three conditions: CBT-I plus bright light therapy, CBT-I plus placebo light therapy, or a waiting-list control group.
The active intervention will consist of six weekly group-based CBT-I sessions, with daily morning light treatment beginning from the second week of intervention. Participants in the bright light therapy group will receive active blue-green light treatment delivered by light therapy glasses, whereas those in the CBT-I only group will receive placebo light therapy delivered via the same device. Assessments will be conducted at baseline and post-treatment for all the study participants, and additionally 1-month follow-up and 6-month follow-up for those in the two active intervention groups to evaluate the immediate and maintenance effects of the treatment. Outcome measures will include self-reported, clinician-rated, and objective assessments of sleep, circadian rhythm, arousal, ADHD symptoms, mood symptoms, cognitive functioning, and other daytime functioning outcomes.
shirley.li@hku.hk+852 3917-7035