Actively Recruiting
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
Eligibility Criteria
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
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
Trial Site Locations
Total: 1 location
1
Sungshin Women's University
Seoul, South Korea, 02844
Actively Recruiting
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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