Actively Recruiting

Phase Not Applicable
Age: 18Years - 26Years
All Genders
Healthy Volunteers
NCT06853106

Digital Sleep Program for College Students with Insomnia

Led by Taipei Medical University · Updated on 2025-02-28

90

Participants Needed

1

Research Sites

170 weeks

Total Duration

On this page

Sponsors

T

Taipei Medical University

Lead Sponsor

N

National Science and Technology Council, Taiwan

Collaborating Sponsor

AI-Summary

What this Trial Is About

This randomized controlled trial (RCT) study aims to evaluate the effectiveness of a digital-based multimodal sleep management program compared to a waitlist control group in improving sleep-related outcomes, including insomnia severity, daytime sleepiness, objective sleep parameters, and sleep reactivity to stress, as well as psychological health indices, such as depression, anxiety, and resilience. Additionally, this study seeks to examine the mediating role of different chronotypes in the effectiveness of the sleep intervention on the outcomes of interest.

CONDITIONS

Official Title

Digital Sleep Program for College Students with Insomnia

Who Can Participate

Age: 18Years - 26Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Registered as a full-time student
  • Aged 18 to 26 years old
  • Experiencing insomnia for at least three months
  • Currently own and use a personal mobile device
  • Ability to read and speak Chinese
  • Not taking hypnotics, sedatives, or antidepressants
  • Not pregnant or lactating
Not Eligible

You will not qualify if you...

  • Using a smartphone model that cannot support the app
  • Currently using other sleep program apps
  • Meeting a STOP-BANG score of 653

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

Taipei Medicine University

Taipei, Taiwan, 11031

Actively Recruiting

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Research Team

P

Pei-Shan Tsai, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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