Actively Recruiting

Phase Not Applicable
Age: 12Years - 24Years
All Genders
NCT07399964

Effects of CBT-I on Impulsivity and Risk Taking in Youths With Insomnia

Led by The University of Hong Kong · Updated on 2026-02-10

124

Participants Needed

1

Research Sites

127 weeks

Total Duration

On this page

Sponsors

T

The University of Hong Kong

Lead Sponsor

C

Chinese University of Hong Kong

Collaborating Sponsor

AI-Summary

What this Trial Is About

Insomnia is prevalent in adolescents. Impulsive behaviours and excessive risk-taking have been linked to the manifestation of psychopathology in youths. Previous research based on behavioural and neurophysiological measures has found that individuals with insomnia demonstrated impaired inhibitory control, which is associated with detrimental outcomes such as substance abuse and self-harm. Existing evidence has shown some positive effects of cognitive behavioural therapy for insomnia (CBT-I) on insomnia symptoms and daytime functioning in youths. Given the link between insomnia and impulsivity reported in previous research, and sleep as a highly modifiable factor, we are conducting this randomised controlled trial to examine the impact of CBT-I in improving impulsivity and risk-taking in youth with insomnia.

CONDITIONS

Official Title

Effects of CBT-I on Impulsivity and Risk Taking in Youths With Insomnia

Who Can Participate

Age: 12Years - 24Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Chinese individuals aged 12 to 24 years old
  • Written informed consent provided by participant and parent/guardian if under 18
  • Willing to comply with the study protocol
  • Diagnosed with insomnia disorder according to DSM-V criteria
  • Insomnia Severity Index (ISI) score of 9 or higher
Not Eligible

You will not qualify if you...

  • Current diagnosis of substance abuse or dependence
  • History of manic or hypomanic episodes, schizophrenia spectrum disorders, neurodevelopmental disorders, organic mental disorders, or intellectual disabilities
  • Medical conditions known to affect sleep quality (e.g., eczema, gastro-oesophageal reflux disease)
  • Clinically diagnosed sleep disorders other than insomnia (e.g., narcolepsy, sleep-disordered breathing, restless leg syndrome)
  • Regular use of medications affecting sleep (including hypnotics, steroids, melatonin, Traditional Chinese Medicine)
  • Clinically significant suicidality (suicidal ideation with plan or attempt)
  • Currently receiving psychological treatment for insomnia
  • Hearing or speech deficits
  • Night shift work

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sleep Research Clinic and Laboratory, Department of Psychology, The University of Hong Kong

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

S

Shirley Xin LI, DClinPsy, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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