Actively Recruiting

Phase Not Applicable
Age: 6Months - 24Months
All Genders
Healthy Volunteers
NCT05806450

Development of Sleep Intervention for Parent and Child

Led by Sungshin Women's University · Updated on 2025-05-14

190

Participants Needed

1

Research Sites

120 weeks

Total Duration

On this page

Sponsors

S

Sungshin Women's University

Lead Sponsor

N

National Research Foundation of Korea

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study aims to develop and test the intervention program to help manage parental thoughts in parents with child sleep problems.

CONDITIONS

Official Title

Development of Sleep Intervention for Parent and Child

Who Can Participate

Age: 6Months - 24Months
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Child's primary nighttime caregiver (mothers or fathers) of full-term, healthy, singleton, 6 to 24 months old
  • Caregiver participants aged between 19 to 65 years
  • The caregiver who is a native speaker of Korean (a person who is able to listen, speak, and write in Korean, and does not have any difficulties in understanding the Korean language)
  • Residents of South Korea
  • Sleep arrangements without restriction for using an auto-videosomnography device: (1) parent-child sleep separately (one should not change the sleep arrangement only for the participation in the study); (2) if parents and child share a bed, the child's own space should be large enough for the videosomnography camera to capture child body solely.
  • Be available on devices with the camera (e.g., tablets, personal computers) for the online intervention/session
Not Eligible

You will not qualify if you...

  • Child's gestational age before 37 weeks or after 42 weeks
  • Children with developmental disability
  • Caregiver participant (or partner) who is currently working the night shift or night duty
  • Caregiver participant who has a history of sleep disorders besides insomnia
  • Caregiver participant who has lifetime bipolar disorder, schizophrenia spectrum, and other psychotic disorders, alcohol, caffeine, or other substance substance-related disorders, neurocognitive disorders, thyroid-related disorders, or epilepsy
  • Caregiver participant who is currently experiencing a major depressive disorder, panic disorder (only if 64 4 nocturnal panic attacks in the past month), or post-traumatic stress-related problems
  • Caregiver participant who is using medications or substances that directly affect sleep
  • Caregiver participant who is currently getting cognitive behavioral therapy for insomnia (CBTi)
  • Pregnant women

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

Sungshin Women's University

Seoul, South Korea, 02844

Actively Recruiting

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Research Team

S

Sooyeon Suh, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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