- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07599566
Parenting in the Preschool System in Malaysia
Cluster Randomised Trial of a Hybrid Human-digital Playful Parenting Programme in the Malaysian Preschool System
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.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
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.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
-
-
-
Kuala Lumpur, Malezja
- Universiti Putra Malaysia
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Opis
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
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Zapobieganie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Pojedynczy
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: Intervention Group
Intervention group participants will receive one in-person onboarding session, NKText - a self-guided chatbot providing parenting support, and facilitated WhatsApp support groups.
|
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".
|
|
Brak interwencji: Control Group
The control group will not receive the intervention until after the completion of the intervention period and the final follow-up data collection.
Throughout the study period, participants in all groups may access any other interventions, programs, or services that are not part of the study intervention.
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Child early learning and development
Ramy czasowe: 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.
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Positive Parenting
Ramy czasowe: 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.
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Child Literacy and Numeracy
Ramy czasowe: 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.
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Parent involvement in playful learning
Ramy czasowe: 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)
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Child Maltreatment
Ramy czasowe: 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)
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Child externalising symptoms
Ramy czasowe: 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
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Parenting Stress
Ramy czasowe: 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
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Anxiety and depression
Ramy czasowe: 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
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Father involvement with the child
Ramy czasowe: 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.
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Gender equitable behaviours
Ramy czasowe: 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
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Co-parenting support
Ramy czasowe: 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.
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Marital health/quality
Ramy czasowe: 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
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Intimate partner violence
Ramy czasowe: 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.
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
|
Financial Stress
Ramy czasowe: 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.
|
Baseline, 3-5 months post-baseline, 12-15 months post-baseline
|
Współpracownicy i badacze
Sponsor
Współpracownicy
Publikacje i pomocne linki
Przydatne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- R94406/RE001
- 10.17605/OSF.IO/AZ3NY (Identyfikator rejestru: Prospectively registered on Open Science Framework on 17/08/24; ClinicalTrials.gov entry retrospective and consistent.)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Ramy czasowe udostępniania IPD
Kryteria dostępu do udostępniania IPD
Typ informacji pomocniczych dotyczących udostępniania IPD
- PROTOKÓŁ BADANIA
- SOK ROŚLINNY
- ICF
- ANALITYCZNY_KOD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .
Badania kliniczne na Zachowanie dziecka
-
Stanford UniversityNational Cancer Institute (NCI)ZakończonyNawracający rak wątrobowokomórkowy | Child-Pugh Klasa A | Child-Pugh Klasa BStany Zjednoczone, Japonia
-
Centre Hospitalier Universitaire DijonZakończonyChild-Pugh Rak wątrobowokomórkowyFrancja
-
Ohio State University Comprehensive Cancer CenterVarian Medical SystemsZakończonyChild-Pugh Klasa A | Rak wątrobowokomórkowy stopnia IIIA | Rak wątrobowokomórkowy w stadium IIIB | Rak wątrobowokomórkowy stopnia IIIC | Rak wątrobowokomórkowy w stadium IVA | Rak wątrobowokomórkowy w stadium IVB | Child-Pugh Klasa BStany Zjednoczone
-
Boehringer IngelheimNie dostępnyChoroby płuc, śródmiąższowe (w populacjach pediatrycznych) | Śródmiąższowa choroba płuc wieku dziecięcego (chILD)
-
MindRank AI LtdJeszcze nie rekrutacjaZaburzenia czynności wątroby (łagodne i umiarkowane, klasa A i B wg Child-Pugh) | Niewydolność wątroby (MeSH ID: D048550)Chiny
-
CatalYm GmbHRekrutacyjnyChild-Pugh Rak wątrobowokomórkowy | Nieoperacyjny lub przerzutowy rak wątrobowokomórkowy | Niepowodzenie leczenia pierwszej linii obejmującego zatwierdzony związek anty-PD-(L)1Włochy, Niemcy
-
Roswell Park Cancer InstituteMerck Sharp & Dohme LLCZakończonyZaawansowany rak wątrobowokomórkowy dorosłych | Child-Pugh Klasa A | Rak wątrobowokomórkowy III stopnia | Rak wątrobowokomórkowy stopnia IIIA | Rak wątrobowokomórkowy w stadium IIIB | Rak wątrobowokomórkowy stopnia IIIC | Rak wątrobowokomórkowy IV stopnia | Rak wątrobowokomórkowy w stadium IVA | Rak wątrobowokomórkowy...Stany Zjednoczone
-
AstraZenecaZakończonyRak żołądka | Zaawansowane nowotwory lite | Guz lity | Child-Pugh A do B7 Zaawansowany rak wątrobowokomórkowy | NSCLC z mutacją EGFR i/lub ROS | Rak z przerzutami do płucRepublika Korei