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Clinical Trials in China / NCT07420504
Starting soon Not applicable

A Longitudinal Study of Parental Sleep Intervention for Behavioral Insomnia in Early Childhood

NCT07420504 · tracked via the Priya Life Science China tracker
Sponsor
Children's Hospital of Soochow University
Phase
Not applicable
Started
2026-08
Last updated
2026-07-10

Condition(s) studied

Behavioural Insomnia of Childhood

Investigational drug(s) / intervention(s)

Parental sleep enhancement intervention

Parental sleep enhancement intervention: The sleep intervention toolkit for this project is designed based on relevant research and guidelines. Two structured parental intervention sessions, each lasting 2 hours, will be conducted by qualified paediatricians in an intervention room within the Department of Child Health. The first session will be held within 2 weeks after the baseline evaluation, followed by the second session 2 weeks later. Up to 3 caregivers per child may attend, at least one of whom must be a parent. Each session will accommodate a maximum of three families. Adherence to the intervention will be enhanced through health education on child sleep, sharing each child's sleep status to guide tailored intervention plans, as well as providing timely sleep and developmental reports during the intervention and at each follow-up visit.

Study summary

The global incidence of mental illness among children and adolescents is rising, drawing increasing attention to early risk factors and preventive strategies. Behavioral sleep problems, which affect up to 50% of infants in the local population, are closely linked to impaired self-regulation-a core factor underlying many psychological disorders and a promising target for early intervention. Enhancing self-regulation may not only alleviate sleep problems but also mitigate long-term mental health risks. This study aims to develop an intervention toolkit based on current guidelines and high-quality evidence, integrating parent education with dynamic sleep assessment and longitudinal evaluation of self-regulation in infants. The project seeks to establish the efficacy of this approach, identify moderators of intervention outcomes, and provide an evidence base for personalized sleep interventions in clinical practice.

Eligibility

Sex
ALL
Min age
6 Months
Max age
36 Months
Healthy volunteers
No
Inclusion Criteria: 1. Children aged 6-36 months 2. Diagnosed with behavioural insomnia (sleep latency \> 20 minutes and/or ≥ 2 nighttime awakenings per night, each lasting at least 5 minutes) 3. Daytime functional impairment (eg., excessive sleepiness, inattention, emotional problems) 4. Parental consent for participation Exclusion Criteria: 1. Chronic diseases 2. History of head trauma 3. Other primary sleep disorders (e.g., obstructive sleep disorder, narcolepsy, restless leg syndrome) 4. Developmental delay, epilepsy, or other neurological/metabolic disorders 5. Participation in a new intervention program within the past 4 weeks, and/or initiation of new medication within the past 4 weeks.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Childrens' Hospital of Soochow University Suzhou Jiangsu

More Children's Hospital of Soochow University trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07420504 on ClinicalTrials.gov ↗ ← All trials in China