Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07420504

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

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.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

6 month–36 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Childrens' Hospital of Soochow University

Suzhou, Jiangsu, China

Location contact

Tingyu Rong, Doctor

CONTACT

[email protected]

86+0512-80691135

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children aged 6-36 months
  • Diagnosed with behavioural insomnia (sleep latency > 20 minutes and/or ≥ 2 nighttime awakenings per night, each lasting at least 5 minutes)
  • Daytime functional impairment (eg., excessive sleepiness, inattention, emotional problems)
  • Parental consent for participation

Exclusion criteria

  • Chronic diseases
  • History of head trauma
  • Other primary sleep disorders (e.g., obstructive sleep disorder, narcolepsy, restless leg syndrome)
  • Developmental delay, epilepsy, or other neurological/metabolic disorders
  • Participation in a new intervention program within the past 4 weeks, and/or initiation of new medication within the past 4 weeks.

Treatment and study plan

Parental sleep enhancement intervention

Behavioral

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.

Primary outcomes

  1. Sleep efficiency (SE) measured by Actigraphy

    Time frame: Baseline, 1 month, 6 months and 12 months

    Sleep efficiency is defined as the percentage of total sleep time (sleep period determined by the actigraphy) to the total time spent in bed (from the time children go to bed to the time they finally get up in the morning). A higher percentage reflects more continuous and higher-quality sleep. As SE is closely related to SOL and nighttime awakings, it is selected as the primary outcome of the current study.Through the built-in accelerometer and other sensors, the actigraphy can be used to monitor an individual's activity level and sleep situation, thereby analysing the child's sleep patterns such as sleep efficiency. The team technician will export the relevant sleep indicators recorded by the actigraphy and calculate relevant outcome measures. Moreover, the actigraphy is validated with parental records of sleep diaries.

Secondary outcomes

  1. Sleep onset latency (SOL) measured by Actigraphy

    Time frame: Baseline, 1 month, 6 months and 12 months

    In this study, SOL serves as the indicator of sleep initiation difficulty, with a threshold exceeding 20 minutes indicating prolonged sleep onset. Improvement in SOL (i.e., shortened latency) following the intervention will suggest enhanced self-regulation capacity and reduced reliance on parental assistance at bedtime. Moreover, the actigraphy is validated with parental records of sleep diaries.

  2. Wake after sleep onset (WASO) measured by Actigraphy

    Time frame: Baseline, 1 month, 6 months, and 12 months

    Wake after sleep onset (WASO) is defined as the total duration of wakefulness between initial sleep onset and final morning awakening. Longer WASO indicates poorer nighttime sleep quality. Improvements (reductions) following intervention indicate better sleep consolidation. Moreover, the actigraphy is validated with parental records of sleep diaries.

  3. The number of nighttime awakenings (NW) measured by Actigraphy

    Time frame: Baseline, 1 month, 6 months and 12 months

    The number of nighttime awakenings (NW) refers to the total number of awakening events lasting more than 5 minutes per night. A frequency of two or more awakenings per night may indicate poor nighttime sleep quality. This indicator will be reported to assess the degree of fragmentation of nighttime sleep. Improvements (reductions) following intervention indicate better sleep consolidation. Moreover, the actigraphy is validated with parental records of sleep diaries.

  4. Subjective sleep quality measured by the Brief Infant Sleep Questionnaires (BISQ)

    Time frame: Baseline, 1 month, 6 months, and 12 months

    BISQ is a parent-reported instrument designed to screen for sleep problems in infants and toddlers. This study will use the standardised Chinese version, which covers multiple aspects of early childhood sleep, including sleep onset conditions, total sleep duration, nighttime awakenings, co-sleeping, and overall sleep patterns.

  5. Subjective sleep quality measured by the Infant/Toddler Sleep Assessment Scale (ISAS/TSAS)

    Time frame: Baseline, 1 month, 6 months, and 12 months

    ISAS and TSAS were developed and validated by the Provincial Research Working Group of Chinese Infant and Toddler Sleep Assessment Scale for children aged 4-11 months and 12-35 months, respectively. Total scores, derived from all items, reflect sleep quality, with responses rated on a four-point Likert scale of 1 to 4. Higher scores indicate poorer sleep quality.

  6. Self-regulation ability measured by the Age and Stage Questionnaires: Social and Emotional-2 (ASQ:SE-2)

    Time frame: Baseline, 1 month, 6 months, and 12 months

    The ASQ:SE-2 is an internationally recognised developmental screening tool for assessing social-emotional development in children aged 1 to 72 months.

    The questionnaire assesses a child's development across 7 specific behavioural dimensions:

    • Self-Regulation: ability to calm or settle themselves.
    • Compliance: ability to follow rules and respond to limits.
    • Social-Communication: use of gestures, sounds, and words to interact with others.
    • Adaptive Functioning: ability to manage daily routines like eating, sleeping, and toileting.
    • Autonomy: ability to act independently and demonstrate self-confidence.
    • Affect: expression of feelings and emotions.
    • Interpersonal interaction: ability to engage with parents, other adults and children.

    A higher score indicates more concerning behaviours.

Other outcomes

  1. Maternal excessive daytime sleepiness measured by the Epworth Sleepiness Scale (ESS)

    Time frame: Baseline, 1 month, 6 months, and 12 months

    Maternal daytime sleepiness will be assessed using the Epworth Sleepiness Scale (ESS), an 8-item self-reported questionnaire employing a 4-point Likert scale of 0 to 3. It measures how likely a person is to doze off or fall asleep in 8 common, sedentary situations of daily life. Higher scores indicate greater daytime sleepiness, with a score of 10 or above indicating excessive daytime sleepiness.

  2. Maternal mental health measured by the World Health Organisation Five Well-Being Index (WHO-5)

    Time frame: Baseline, 1 month, 6 months and 12 months

    Maternal mental health will be assessed using the World Health Organization Five Well-Being Index (WHO-5), a 5-item self-reported questionnaire employing a 6-point Likert scale of 0 to 5. These items reflect positive mood, vitality, and general interests over the preceding 14 days. Higher scores indicate greater well-being.

  3. Maternal parenting stress measured by the Parenting Stress Index-Short Form (PSI-SF)

    Time frame: Baseline, 6 months and 12 months

    Maternal parenting stress will be assessed using the Parenting Stress Index-Short Form (PSI-SF), a 36-item parent-reported questionnaire consisting of three subscales including parental distress, parent-child dysfunctional interaction, and difficult child. The total score ranges from 36 to 180. A score of 85 or less indicates a normal level of parental stress. A score between 86 and 90 represents a critically high level. A score greater than 90 suggests a high level of parental stress, and a score of 99 or above indicates an extremely high level of parental stress.

  4. Maternal occupational stress measured by the Chinese Version of Copenhagen Psychosocial Questionnaire (COPSOQ)

    Time frame: Baseline and 12 months

    Maternal occupational stress will be assessed using the short version of the Copenhagen Psychosocial Questionnaire (COPSOQ), a 44-item self-reported questionnaire consisting of eight subscales. Higher scores in the job demands and job insecurity subscales reflect greater occupational stress, whereas higher scores in the personal impact and development, interpersonal relationships and leadership, and job satisfaction subscales indicate lower levels of occupational stress.

  5. Maternal life satisfaction measured by the Satisfaction With Life Scale (SWLS)

    Time frame: Baseline and 12 months

    Maternal life satisfaction will be assessed using the Satisfaction With Life Scale (SWLS), a 5-item self-reported questionnaire employing a 7-point Likert scale of 1 to 7. Higher scores indicate greater perceived life satisfaction.

  6. Mother-child relationship measured by the Postpartum Bonding Questionnaire (PBQ)

    Time frame: Baseline and 12 months

    Mother-child bonding will be assessed using the Postpartum Bonding Questionnaire (PBQ), a 25-item self-reported questionnaire employing a 6-point Likert scale of 0 to 5. Higher scores indicate greater impairment in the mother-child relationship.

  7. Family functioning measured by the Family APGAR Index (APGAR)

    Time frame: Baseline and 12 months

    Maternal satisfaction with family functioning will be assessed using the Family APGAR Index (APGAR), a 5-item self-reported questionnaire employing a 3-point Likert scale of 0 to 2. Scores range from 0 to 10, with higher scores indicating better family functioning (0-3 = highly dysfunctional, 4-6 = moderately dysfunctional, 7-10 = highly functional).

  8. Child temperament measured by the Carey Children Temperament Questionnaire Series

    Time frame: Baseline and 12 months

    Child temperament will be assessed using age-appropriate version of scales, including the Revised Infant Temperament Questionnaire (RITQ) for infants aged 5 to 11 months, and the Toddler Temperament Scale (TTS) for children aged 1 to 3 years. Both questionnaires assess nine subscales: rhythmicity, adaptability, approach, intensity, mood, activity, threshold, distractibility, and persistence.

  9. Child neurodevelopment measured by the Chinese Developmental Scale for Children Aged 0-6 years (CDSC-II)

    Time frame: Baseline, 6 months and 12 months

    Child neurodevelopment will be assessed using the Chinese Developmental Scale for Children Aged 0-6 Years (2nd Edition) (CDSC-II). This scale evaluates five subscales: gross motor, fine motor, adaptive ability, language, and social behaviour, comprising a total of 261 items across 28 age-in-months groups. The development quotient will be used to determine subscale-specific and overall development status, with lower scores signifying developmental vulnerability.

Sponsors and collaborators

Lead sponsor

Children's Hospital of Soochow University

Other

Registry information

Official study title

Efficacy of Parental Sleep Intervention on Infants and Toddlers With Behavioural Insomnia: A Longitudinal Follow-up Study

Acronym: SuSleep

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Feb 19, 2026
Registry last updated
Jul 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.