- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03615937
KeySteps@JC - Early Child Intervention (KSJC)
KeySteps@JC - Early Child Intervention for Underprivileged Families in Hong Kong
Study Overview
Status
Conditions
Detailed Description
Socioeconomic disadvantage permeates multiple levels of environmental contexts in which children are raised, including the family environment and schools. Disparities in life outcomes can be observed in early childhood and developmental gaps widen over time. Continued exposure to adverse conditions propagates the developing child on an increasingly risky trajectory. This study aims to mitigate the adverse effect of socioeconomic disadvantage on children and their families.
This is a clustered randomised controlled study recruiting 32 kindergartens in two underprivileged districts (16 in each district) in Hong Kong. District is a blocking factor. Within each district, 8 kindergartens will be randomised in comprehensive intervention group while the remaining 8 will be in health support group. The families in the comprehensive intervention will receive a holistic package of interventions, including child interactive intervention, family empowerment, and health support. The families in the health support group will only receive health support intervention.
In addition, a stepped wedge cluster randomised control trial design will be used to deliver and evaluate the health intervention package (health seminars/workshops, dental check-up/treatment, visual check-up/treatment). The schematic diagram of the design is shown in the figure below.
Another randomisation will be conducted to determine the sequence in which the health intervention takes place. 4 KGs will be provided with the health intervention in each month sequentially from Nov 2018 to Jun 2019 (totally 8 months). The randomisation should ideally be stratified by district (SSP/TSW) and the original group allocation (Comprehensive/Health). In other words, in each month, 1 KG from SSP Comprehensive, 1 from SSP Health, 1 from TSW Comprehensive, 1 from TSW Health will receive the health intervention package.
In analysis, the time exposed to intervention (e.g. Gp1 exposed to 8 months at Jun 2018) will be used to evaluate the effect of the intervention. Since the time exposed to intervention (i.e. the starting time of the intervention) is randomised, internal validity should be ensured. In addition, the stratification of district and the original group allocation should eliminate the influence of these factors.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Hong Kong, Hong Kong
- The University of Hong Kong
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- K1 children [~3 years], with a selected Pre-Nursery group [~2 years], and their families attending participating kindergartens.
Kindergartens located at Sham Shui Po and Tin Shui Wai districts in Hong Kong based on the following criteria:
- Full-day program
- Pre-Primary Education Voucher Scheme
- Basic school facilities (minimally >1 classroom and a basic activity room available)
- Average school tuition fee in the past 5 years (<HKD 40,000)
- Proportion of teachers with early childhood education bachelor degrees or above. Teachers of participating children will be their facilitators/assessors in this study.
Exclusion Criteria:
- Children and families from non-participating kindergartens; children below and above K1 (except for a selected Pre-Nursery group).
- Non-English/Chinese speaking subjects.
- Teachers of non-participating children and kindergartens.
- Non-consenting subjects.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Comprehensive Intervention
This is a holistic package of interventions, including:
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The Child Interactive Intervention will be delivered through a Dialogic Reading Program, which is an individual/group level intervention component for both families and kindergartens.
The original Dialogic Reading Program aims to enhance children's literacy and oral language skills by using the specific technique of shared book reading developed by Whitehurst and colleagues (1988).
However, this project will expand from the original Dialogic Reading Program template to include alignment with local kindergarten curriculum and themed interactive activities that help build social competence and emotional maturity in children, in addition to cognitive skills.
Family empowerment in this project can be conceptualized across three main pillars: 1) adaptive parenting; 2) adaptive extended family environment; and 3) familial resources.
Typically, adaptive parenting is translated into positive parenting programs for primary caregivers, and the rest of the family environment involves extended caregivers.
However, families from disadvantaged environments encounter many hurdles that hinder effective parenting and relationship nurturing, and parents' mental wellbeing are also consistently impacted by competing demands.
A new model of Community Hub will be implemented and there will be two hubs established in two respective districts.
The Community Hubs act as an alternative venue to implement service delivery of intervention packages, such as activity sessions in the Child Interactive Intervention, Parenting Program, and mentor-mentee experience exchange, which provide families institutional flexibility and extended support while internalizing new practices.
There will also be health education, consultation support and developmental assessments.
The Hubs will play the roles of promoting and interweaving play-based learning into the lives of families frequently faced with competing demands and a lack of resources, and enable a protracted network for parents.
This intervention package aims at providing a better physical and social kindergarten environment to maximize developmental reach and expedite timely interception and feedback without adding burden to teachers and frontline service professionals.
Health seminars and interactive workshop will be provided to the families.
Screen for common child health problems (e.g.
dental and visual) will also be conducted.
A support hotline and website will be established for the participants.
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Active Comparator: Health Support
This is a control arm with only health components. 1. Health education, screening, and support |
Health seminars and interactive workshop will be provided to the families.
Screen for common child health problems (e.g.
dental and visual) will also be conducted.
A support hotline and website will be established for the participants.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Child development
Time Frame: Three years after start of intervention
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Full scale score of Hong Kong Early Child Development Scale (HKECDS); The HKECDS includes items from the following eight subscales: Personal, Social and Self-Care (7 items), Language Development (13 items), Pre-academic Learning (27 items), Cognitive Development (10 items), Gross Motor (12 items), Fine Motor (9 items), Physical Fitness, Health and Safety (7 items), and Self and Society (10 items).
The items are scored on a 0/1 basis.
The subscale items can be summed to a total score.
Higher score indicate better developmental outcomes.
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Three years after start of intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Physical health and well-being
Time Frame: Three years after start of intervention
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Aggregated score based on physical and health assessments such as body height and weight, blood pressure, spirometry, ultrasound measured bone density, and skin prick test using principal component analysis
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Three years after start of intervention
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Socio-emotional development
Time Frame: Three years after start of intervention
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Aggregated score based on validated tools such as Strength and Difficulties Questionnaires and Chinese Early Development Instrument using principal component analysis
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Three years after start of intervention
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Neurocognitive development
Time Frame: Three years after start of intervention
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Aggregated score based on validated tools such as Hong Kong Early Child Development Scale and Parents' Evaluation of Developmental Status using principal component analysis
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Three years after start of intervention
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Parental Capacity and Parenting Practices
Time Frame: Three years after start of intervention
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Aggregated score based on validated tools such as Parent-child Conflict Tactics Scale using principal component analysis
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Three years after start of intervention
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Parenting and developmental literacy
Time Frame: Three years after start of intervention
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Aggregated score based on validated tools such as Parent-Child Interaction Scale, Parenting Styles and Dimensions Questionnaire using principal component analysis
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Three years after start of intervention
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Parental mental health and emotion processing
Time Frame: Three years after start of intervention
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Aggregated score based on validated tools, such as General Self-Efficacy Scale, Connor Davidson Resilience Scale using principal component analysis
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Three years after start of intervention
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School readiness
Time Frame: Three years after start of intervention
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Total scale score of the Chinese Early Development Instrument using principal component analysis
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Three years after start of intervention
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Patrick Ip, The University of Hong Kong
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- KeySteps@JC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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