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OpenTrials
Completed

NCT Number: NCT07599566

Parenting in the Preschool System in Malaysia

This study aims to evaluate the effectiveness of a hybrid human-digital playful parenting programme, "Naungan Kasih-Hybrid (NK-Hybrid)", in Malaysia. The programme is facilitated by teachers from Malaysian preschools for low-income families, consisting of a) one in-person session to introduce caregivers to the programme, b) teacher-facilitated WhatsApp support groups, and c) an interactive chatbot-led parenting programme featured on WhatsApp, called "Naungan Kasih-Text (NKText)". It tests the effectiveness of this package in a cluster-randomised trial, with 50 preschools as clusters, randomly assigned to either the treatment group or a waitlist control group. Findings from this study will provide evidence for the effectiveness of a low-cost and scalable intervention integrating digital modalities with a "light-touch" in-person component to improve educational outcomes in children attending preschools for low-income families, and thereby address social inequalities in Malaysia.

N = 50 Clusters, 772 Primary Caregivers, 304 Secondary Caregivers, and 754 Children. Enrolment reflects participating primary caregivers.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Universiti Putra Malaysia

Kuala Lumpur, Malaysia

About this study

The primary aims of the study are to:

Evaluate the effectiveness of NK-Hybrid on positive parenting at three months post-baseline in comparison to wait-list controls Evaluate the effectiveness of NK-Hybrid on child learning and development, as measured by parent and teacher reports of language and communication, literacy, socioemotional, and numeracy skills, and by direct assessments of literacy and numeracy skills, at approximately 12 months post-baseline in comparison to wait-list controls

Secondary aims of the study include:

Evaluate the sustained effectiveness of NK-Hybrid on positive parenting at approximately 12 months post-baseline.

Evaluate the effectiveness of NK-Hybrid on children's learning, namely their literacy and numeracy skills, in comparison to the control group, at three months post-baseline Evaluate the effectiveness of NK-Hybrid on secondary outcomes - parent involvement in playful learning, child maltreatment (physical and emotional abuse), caregiver anxiety and depression, parenting stress, child externalising symptoms, child learning and development, caregiver financial stress, intimate partner violence, marital health, co-parenting support, father involvement, and gender equitable behaviours - at approximately three months post-baseline and 12 months post-baseline.

Evaluate the intervention costs and cost-effectiveness of NK-Hybrid on primary outcomes of positive parenting and child literacy and numeracy skills.

Evaluate the association between engagement in the NK-Hybrid intervention and primary and secondary outcomes.

Explore potential mediators of positive parenting, child literacy and numeracy skills, child maltreatment, child externalising symptoms, and caregiver depression and anxiety at 12 months post-baseline.

Explore potential moderators of positive parenting, child literacy and numeracy skills, child maltreatment, child externalising symptoms, and caregiver depression and anxiety based on socio-demographics and psychosocial assessments at baseline

In line with the study's primary and secondary objectives, the following hypotheses have been defined a priori and will be evaluated using the methods outlined in this statistical analysis plan.

Hypothesis 1a: Caregivers in the treatment group will show higher levels of positive parenting, in comparison to the control group, at 3 months post-baseline.

Hypothesis 1b: Children in the treatment group will show greater improvements in early learning and development, namely their literacy and numeracy skills, in comparison to the control group, at 12 months post-baseline.

Hypothesis 2a: Caregivers in the treatment group will show higher levels of positive parenting, in comparison to the control group, at 12 months post-baseline.

Hypothesis 2b: Children in the treatment group will show greater improvements in learning, namely their literacy and numeracy skills, in comparison to the control group, at three months post-baseline.

Hypothesis 2c: Caregivers in the treatment group will show lower levels of child maltreatment (physical and emotional abuse), anxiety and depression, parenting stress, child externalising symptoms, financial stress, and intimate partner violence, in comparison to the control group, at 3 months and 12 months post-baseline.

Hypothesis 2d: Caregivers in the treatment group will show higher levels of parent involvement in playful learning, marital health, co-parenting support, father involvement, and gender equitable behaviours in comparison to the control group, at 3 months and 12 months post-baseline.

Hypothesis 3a: The intervention will be more cost-effective than the control condition for the primary outcomes, yielding a cost per unit of effect that supports decision-making by relevant stakeholders.

Hypothesis 3b: Higher engagement with intervention components (i.e., in-person onboarding, NKText, and WhatsApp support groups) will be associated with greater improvements in the aforementioned primary and secondary outcomes.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Preschools (clusters):

  • Registered Ministry of Rural Development (KEMAS) preschool
  • Has a class of 20 or more children aged 4-6 years
  • Selected by KEMAS leadership as available to participate
  • Class teacher is willing to deliver the programme and participates in programme training

Parents/Caregivers:

  • Responsible for a child aged 4-6 years enrolled in a participating KEMAS preschool
  • Aged 18 years or older
  • Has access to a mobile phone compatible with WhatsApp
  • Provides informed consent

Children:

  • Enrolled in a participating KEMAS preschool
  • Aged 4-6 years
  • Parent provides consent
  • Provides verbal assent

Teachers (Facilitators):

  • Registered employee with a KEMAS preschool
  • Aged 18 years or older
  • Diploma/certificate in Early Childhood Education (ECE) or equivalent
  • Provides consent
  • Completed training
  • Available to deliver intervention

Exclusion criteria

  • Parents/caregivers who do not meet inclusion criteria
  • Children who do not meet inclusion criteria

Treatment and study plan

Naungan Kasih Positive Parenting Programme

Behavioral

The programme is facilitated by teachers from Malaysian preschools for low-income families, consisting of a) one in-person session to introduce caregivers to the programme, b) teacher-facilitated WhatsApp support groups, and c) an interactive chatbot-led parenting programme featured on WhatsApp, called "Naungan Kasih-Text".

Primary outcomes

  1. Child early learning and development

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Children's early learning and development (caregiver- and teacher-report) will be measured using 23 items from the National Preschool Standards-Based Curriculum Assessment (Malaysia); scale = 0-2; higher score indicates better outcome.

  2. Positive Parenting

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Positive parenting will be measured using 14 items from the Parenting Young Children Scale (PARYC) (McEachern et al., 2012). (Caregiver Report); (0-6); higher score indicates better outcome.

  3. Child Literacy and Numeracy

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Direct child assessments of child learning and development will be conducted by trained research assistants and assessed using an adapted version of the Remote Assessment of Learning (ReAL) High-Access version (Save the Children International, 2021), specifically the Literacy and Numeracy subscales. 12 domains, total score = mean of % correct for each domain; higher score indicates better outcome.

Secondary outcomes

  1. Parent involvement in playful learning

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Parent involvement in playful learning will be measured using four items from the UNICEF Multiple Indicator Cluster Surveys (MICS) Child Development Module/Family Care Indicators (Kariger et al., 2012). (4 items) (0-8 times in last two weeks) - higher indicates more playful learning activities (better outcome)

  2. Child Maltreatment

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Child maltreatment will be measured using six items from the International Society for the Prevention of Child Abuse and Neglect Child Abuse Screening Tool (Meinck et al., 2018), covering physical violence (two items) and psychological violence (four items). (Parent Report); (0-8 times in last two weeks) - higher indicates more incidence of abuse (worse outcome)

  3. Child externalising symptoms

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Child externalising symptoms will be assessed using 12 items from the externalising subscale of the Child and Adolescent Behavior Inventory (CABI) (Cianchetti et al., 2013); (0-2); higher score indicates worse outcome

  4. Parenting Stress

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Parenting stress will be assessed using six items from the Parenting Stress Scale (Berry & Jones, 2016); (0-5); higher score indicates worse outcome

  5. Anxiety and depression

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Anxiety and depression will be assessed using four items from the Patient Health Questionnaire (PHQ-4) Scale (Kroenke et al., 2009); (0-3); higher score indicates worse outcome

  6. Father involvement with the child

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Father involvement with the child will be assessed using seven items from an adapted version of the Alabama Parenting Questionnaire Involvement Subscale (Frick, 1991); (0-4); higher score indicates better outcome.

  7. Gender equitable behaviours

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Gender equitable behaviours will be assessed using four items informed by measures commonly used in violence prevention research (Abramsky et al., 2020; Doyle et al., 2018); (1-5); higher score indicates better outcome

  8. Co-parenting support

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Co-parenting support will be assessed using six items from the Co-parenting Relationship Scale (Feinberg et al., 2012); (0-3); higher score indicates better outcome.

  9. Marital health/quality

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Marital health/quality will be assessed using five items developed by the research team; (1-5); higher score indicates better outcome

  10. Intimate partner violence

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Intimate partner violence will be assessed using four items adapted from the World Health Organisation study on women's health and domestic violence against women (World Health Organization, 2005); (0-3); higher score indicates worse outcome.

  11. Financial Stress

    Time frame: Baseline, 3-5 months post-baseline, 12-15 months post-baseline

    Financial stress will be assessed using six items adapted from the Financial Self-Efficacy Scale (Lown, 2012); (0-3); higher score indicates worse outcome.

Sponsors and collaborators

Lead sponsor

University of Oxford

Other

Collaborators

  • Universiti Putra Malaysia

Registry information

Official study title

Cluster Randomised Trial of a Hybrid Human-digital Playful Parenting Programme in the Malaysian Preschool System

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
May 20, 2026
Registry last updated
May 27, 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.

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