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Prevention of Insomnia in At-risk Youth

NCT05451524 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 204

Last updated 2025-07-10

No results posted yet for this study

Summary

This study aims to conduct a randomized controlled trial in comparing cognitive behavioral insomnia prevention program with the active control group in youths who are at risk of insomnia. The results of this study will allow us to take this potential efficacious prevention program to scale and reduce the associated burden of insomnia in the future.

Conditions

Interventions

BEHAVIORAL

Insomnia prevention program

Youths in the intervention group will receive 4 weekly insomnia prevention program. Each session will last for about 60-90 mins.

BEHAVIORAL

General health education

Youths in the control group will be provided with group-based general health education with same dosage (4 weeks) as intervention group.

Sponsors & Collaborators

  • Chinese University of Hong Kong

    lead OTHER

Principal Investigators

  • NGAN YIN CHAN, PhD · Chinese University of Hong Kong

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
15 Years
Max Age
24 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-07-01
Primary Completion
2026-04-15
Completion
2026-07-15

Countries

  • Hong Kong

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05451524 on ClinicalTrials.gov