Development of Sleep Intervention for Parent and Child

NCT ID: NCT05806450

Last Updated: 2025-05-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

190 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-10

Study Completion Date

2025-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Pediatric sleep problems are common and persistent, which result in negative outcomes without appropriate intervention. Behavioral sleep interventions (BSI) are evidence-based sleep training methods for improving pediatric sleep. However, parental factors (e.g., parental dysfunctional beliefs about child sleep) can interfere with the implementation of BSI. For example, being too worried or having misperceptions about infant sleep may interfere with the parent's ability to successfully and persistently implement BSIs. Therefore, parental thoughts and beliefs should be considered as an important target in the context of pediatric sleep interventions. This study aims to develop a cognitive intervention that identifies and targets parental misperceptions about child's sleep, and test the efficacy of the intervention through a randomized controlled trial.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Behavioral Insomnia of Childhood

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Intervention condition

Structured online intervention consists of three weekly sessions of cognitive therapy and psychoeducation about child sleep

Group Type EXPERIMENTAL

Intervention

Intervention Type BEHAVIORAL

Structured online intervention consists of three weekly sessions of cognitive therapy and psychoeducation about child sleep

Active control condition

Psychoeducation about basic sleep structure and sleep hygiene

Group Type ACTIVE_COMPARATOR

Active control condition

Intervention Type OTHER

Psychoeducation about basic sleep structure and sleep hygiene

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Intervention

Structured online intervention consists of three weekly sessions of cognitive therapy and psychoeducation about child sleep

Intervention Type BEHAVIORAL

Active control condition

Psychoeducation about basic sleep structure and sleep hygiene

Intervention Type OTHER

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Sleep Intervention for Mother and BAby (SIMBA)

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 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

Exclusion Criteria

* 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 ≥ 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
Minimum Eligible Age

6 Months

Maximum Eligible Age

24 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Research Foundation of Korea

OTHER

Sponsor Role collaborator

Sungshin Women's University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Sooyeon Suh

Associate professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Sooyeon Suh, PhD

Role: PRINCIPAL_INVESTIGATOR

Sungshin Women's University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Sungshin Women's University

Seoul, , South Korea

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

South Korea

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Sooyeon Suh, PhD

Role: CONTACT

+82-2-920-7215

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

NRF-2021S1A5A2A03061721

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Digital CBT-I for Chronic Insomnia
NCT06695000 NOT_YET_RECRUITING NA
Helping Young Children Sleep
NCT01729715 COMPLETED NA
Cognitive-Behavior Therapy for Insomnia
NCT00869934 COMPLETED PHASE4
Sleep Interventions and Neurocognitive Outcomes
NCT05987007 NOT_YET_RECRUITING NA