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Enhancing the Ongoing ECD Scale-up Programme (Saving Bangladeshi Babies Brain (SB3) in Bangladesh

Extending and Enhancing the Ongoing Early Childhood Development (ECD) Scale-up Programme (Saving Bangladeshi Babies Brain (SB3) in Bangladesh

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07472699
Acronym
ECD SB3
Enrollment
2400
Registered
2026-03-16
Start date
2024-08-01
Completion date
2026-12-31
Last updated
2026-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Early Child Brain Development

Brief summary

Background (brief): 1. Burden: Globally 250 million children under 5 years of age in developing countries do not reach their full potential due to poverty, malnutrition, and lack of a stimulating environment. 2. Knowledge gap: The early childhood intervention curriculum 'Reach up & Learn' has been adapted for Bangladesh and were successfully used in 10 trials including two trials integrated with Primary Health Care (PHC) services implemented in Community Clinics. Based on the success of the last two studies, the current programme 'Saving Bangladeshi Babies Brains (SB3)' is conducted in 4 districts. Under this programme, a small cluster randomised controlled trial (cRCT) was conducted and found no benefit on child development. However, the programme involved implementation challanges. Therefore, there is a need to determine the strategies to mitigate the challenges and conduct another round of cRCT to test the effectiveness of the strategies on the child development outcomes. 3. Relevance: Bangladesh Govt acknowledges the need for improving children's development and has agreed to collaborate and implement early childhood development (ECD) activities at large scale. Hypothesis (if any): The Investigators hypothesize that the identified strategies would be effective in improving children's development. Objectives: 1. To identify the potential strategies to promote the quality and fidelity of the SB3 early childhood parenting programme integrated into government health care services. 2. To measure the effectivity of the intervnetion on the cogntion, langauge, motor development, and beahvior of the children and maternal parenting knowledge and quality of stimulation at home. Methods: A mixed-method data collection has been conducted and three potential strategies were identified: raising community awareness, increasing health worker's motivation to deliver a quality programme, and the revised curriculum by replacing mothers' made toys to the supplied toys from the progarmme. These startegies will be piloted. And based on the pilot findings, two strategies will be selected to test the effectiveness on child development using a cluster randomised controlled trial design. In the cluster RCT, there will be two arms : i) intervnetion arm I: regular curriclum, ii) intervnetion arm II: revised curriculum and iii) Unique control. Twenty unions from each programme running district will be randomly selected and then randomly allocated to intervention arm I & II . A four non-programme running districts located at the border of the programme districts will be selected as unique control. The children will be tested at the beginning and the end of the 6 months of intervention. Outcome measures/variables: The primary outcomes are children's cognition, and language development and the secondary outcomes are children's behaviour and growth, maternal knowledge on child care and their practices, home stimulation and maternal depressive symptoms.

Interventions

Intervention Arm 1: Pschosocial stimulation intervention using toys made by the programme.

BEHAVIORALCombined

Intervention Arm 2: Psychosocial stimulation intervnetion using toys made by mothers.

Sponsors

International Centre for Diarrhoeal Disease Research, Bangladesh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Months to 24 Months
Healthy volunteers
Yes

Inclusion criteria

* Moderately and severely malnourished children aged 6-24 months of both sexes and whose parents agree to participate in the programme. * Mid-upper arm circumference (MUAC)\<13.5cm will be used to define malnutrition * Maternal education qualification less than 8th grade * Monthly family income BDT\<15000

Exclusion criteria

* Children with MUAC≥13.5 cm * Those whose parents do not consent to participate

Design outcomes

Primary

MeasureTime frameDescription
LanguageFrom enriollment to after 6 months intervention.Children's language will be assessed using the psychometric tool named "Bayley Scale of Infant and Toddler Development Version-IV'. Language subscale contains two components: receptive and expressive test.
Cognitive developmentFrom enrollment to the end of intervention after 6 monthsThe primary outcomes are children's cognition, which will be assessed using the psychometric tool named "Bayley Scale of Infant and Toddler Development Version-IV'. The cognition scales include a series of developmental play tasks based on different abilities like memory, problem solving skill, number concepts, etc.

Secondary

MeasureTime frameDescription
Children's weightFrom enrollment to the end of intervention after 6 monthsWeight measurement in Kg
Children's lengthFrom enrollment to the end of intervention after 6 monthsLength in Cm
Home stimulationFrom enrollment to the end of intervention after 6 monthsChildren's home stimulation will be assessed using Family Care Indicator (FCI)
Maternal depressionFrom enrollment to the end of intervention after 6 monthsMaternal depressive symptoms will be assessed using the shortened version Centre for Epidemiological Studies-Depression scale
Maternal knowledge on child caring practicesFrom enrollment to the end of intervention after 6 months.Maternal knowledge on child caring practices will be assessed using a structured questionnaire.
Children's BehaviorFrom enrollment to the end of intervention after 6 monthsChildren's behavior will be assessed using the Wolke's Behavior Rating Scale during the cognitive and language assessment period.

Countries

Bangladesh

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026