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Clinical Trials/NCT02839148
NCT02839148CompletedNot Applicable

Assessment of Maternal Perception Regarding Childhood Stunting and Development of a Tool to Assess Appetite in Children

International Centre for Diarrhoeal Disease Research, Bangladesh1 site in 1 country390 target enrollmentStarted: April 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
390
Locations
1
Primary Endpoint
Assessment of appetite score of stunted children aged 12-18 months compared to non-stunted children

Study Overview

Brief Summary

This study will provide a tool for researchers to measure important outcomes in relation to trial of intervention to reduce or prevent stunting.

Hypothesis: We assume that appetite score will be associated with improvement in growth and development parameters of children given the nutrition and psychosocial stimulation intervention

Objectives:

To explore maternal perception regarding childhood stunting To develop and validate an appetite measuring tool To assess the appetite status of young children To examine the relationship between appetite score, growth and development, potential biomarkers of appetite, child food intake and intestinal inflammation of the children.

Methods: In the first phase, a qualitative study will be conducted to explore maternal perception regarding childhood stunting and to develop a tool- the "Early Childhood Appetite and Satiety Tool"(ECAST) using mixed method approach (qualitative and quantitative). In the second phase, a community-based trial will be conducted with 50 stunted children of aged 12-18 months, living in urban slums of Dhaka, and 50 age-sex matched control children (non-stunted).

Detailed Description

The stunted children will receive an intervention package which includes food supplementation (FS) with one egg and 150 ml of whole milk supplementing the usual home diet, 6 days a week for 3 months; psychosocial stimulation (PS) for 6 months, and routine clinical care monthly for 6 months. The control children will receive routine clinical care but no FS and PS. Routine clinical care includes micronutrients powder, de-worming, health and nutrition education and immunization. All children will be assessed for appetite score (ECAST score) and anthropometry-at baseline then monthly for 6 months; food intake at baseline then monthly for 3 months, and cognitive development using Bayley Scales of Infant and Toddler Development, third version (Bayley-III) on enrolment and at 3 and 6 months of enrolment. Blood samples will be collected to examine gut hormones, complete blood count and haemoglobin percentage.

Stool samples will be collected for routine examination and stool biomarkers. Urine sample will be collected for screening urinary tract infection. All the specimens will be collected at baseline and at 3 and 6 months of enrollment.

Outcome measures/variables:

The primary outcome:

Assessment of appetite score of stunted children aged 12-18 months compared to non-stunted children.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
6 Months to 5 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •50 stunted children (LAZ<-2) aged 12-18 months
  • •50 non-stunted (LAZ≥-2) aged 12-18 months

Exclusion Criteria

  • •Severe acute malnutrition (SAM)
  • •Chronic illness
  • •Congenital anomaly/developmental delay/oromotor dysfunction

Arms & Interventions

Dietary supplementation

Experimental

In case of dietary supplementation, we will provide milk and egg 6 days a week for 3 months to stunted children.

Intervention: Food supplementation (Dietary Supplement)

psychosocial stimulation

Experimental

In case of psychosocial stimulation, we well provide PS weekly for first month, fortnightly for 2nd and 3rd months and then monthly for next 3 months. The total number of visits will be 11 over a period of 6 months.

Intervention: Food supplementation (Dietary Supplement)

Outcomes

Primary Outcomes

Assessment of appetite score of stunted children aged 12-18 months compared to non-stunted children

Time Frame: 4 months

Secondary Outcomes

  • Association of appetite score with growth and development child food intake(15 months)
  • Association of appetite score with growth and potential biomarkers of appetite(15 months)
  • Association of appetite score with growth and intestinal inflammation of the children(15 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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