- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03891589
Optimized Complementary Feeding With or Without Home Fortification Prevents Decrease of Micronutrient and Growth
March 24, 2019 updated by: Kadek Tresna Adhi, Udayana University
Promotion of Optimized Complementary Feeding With or Without Home Fortification (Taburia) Prevents the Decrease of Nutrient Intake, Level of Micronutrient, and Anthropometric Indices, Also Digestive Health Among Under-Five Children
Malnourished among under-five children characterized by growth faltering is a public health concern in Indonesia.
It requires serious action from the governments because of the prevalence of underweight, stunting, and wasting are increasing.
These impacts are irreversible resulting in the low quality of future human resources.
Several studies showed that growth faltering among under-five children starts at age six months when the amount of breastmilk reduced, complementary feeding initiated, and risk for infection is increased.
A rapid growth phase also causes growth faltering at age 6-24 months.
The inadequate amount and low quality of food during this period can also lead to reducing nutritional status.
The Indonesian Government released a national policy in 2013 to address undernutrition among under-five children called the Indonesia President Regulation No. 42/2013 regarding national movements on the acceleration of nutritional programs to address micronutrients deficiency among under-five children by providing micronutrient powder (MNP) (called Taburia) for children aged 6 - 59 months.
Our literature review documented that there is no study ever conducted to evaluate the effectiveness of MNP (Taburia) in improving the weight and height of the children.
Moreover, behavioral modification interventions to promote food diversification to improve nutrient intake and to prevent micronutrient deficiency are also never conducted.
Based on the rationale and study concept, the following hypotheses are 1).
Promotion of optimized complementary feeding along with or without multi-micronutrient powder or MNP (namely taburia) can prevent reductions in nutrient intake and density; serum ferritin and zinc levels; and anthropometric z-score index compared to controls, and 2) provision of MNP can prevent reductions in nutrient intake and density; serum ferritin and zinc levels; and anthropometric z-score index compared to controls.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Our study consists of two phases.
The first phase was to develop a combination model of Complementary Feeding Recommendation (CFR) or optimized Complementary Feeding (CF) with or without MNP home fortification (Taburia) by using a Linear Programming approach.
The objective of this stage was to address the nutrient gaps.
Also, nutrient analysis of Taburia by employing an LP approach will provide adequate dosing of Taburia to added to local CF.
Several studies have documented that MNP supplementation associated with a reduced bacterial population in digestive systems (Lactobacillus dan Bifidobacterium spp) and induced inflammation on the intestines.
These conditions reduce the absorption capacity of digestive systems leading to nutrient deficiency among under-five children.
Findings from the first phase were an optimized model of CF with or without MNP (Taburia) as an intervention media in the second phase of our study, which evaluates the effectiveness of a combination of CFRs and MNP fortification using an LP approach.
This intervention group compared to (1) optimal Complementary Feeding (CF) with MNP one sachet per week, (2) optimized CF group alone, (3) Provision MNP alone three sachets per week, and (4) control group.
Several indicators to be evaluated were (1) nutrient intake and density; (2) z-score of anthropometric index; (3) micronutrient status; (4) digestive health status (relative population of DNA Bifidobacterium and Lactobacillus spp).
Study Type
Interventional
Enrollment (Actual)
215
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Bali
-
Bangli, Bali, Indonesia, 80614
- Susut District
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
6 months to 11 months (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Under-five children aged 6-11 months (baseline) with normal nutritional status based on weight for height/length z-score (more than -2 SD based on the World Health Organization (WHO) Growth standard (2006))
- Resided in the study location
- Parent or carer agreed to participate in the study and have signed informed consent.
Exclusion Criteria:
- Children with poor nutritional status (<-2SD based on WHZ)
- Families refusing to participate
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Optimized CF with Taburia
The intervention groups consisted of promotion of optimized complementary feeding with home fortification (taburia) one sachet per week
|
These programs were a process of providing information or knowledge to mother of the children consisting of information on initiation of complementary feeding, variety, and frequency of food, nutrient requirements and diet pattern for children (the amount and types of food), and benefits of Taburia.
All this information provided through class-based activities and group discussion by using leaflet and food model conducted by the researchers.
Education materials developed based on CFR models from our previous study by applying the LP approach.
There was also a demonstration on administering complementary feeding (demo and cooking class) to improve skills of the mother on food from selection, design, handling and preparing, based on requirements of the children.
This activity conducted through training once per month for the first four months of the intervention.
Components of complementary feeding promoted in this study are based on CFR using LP approach from our previous research.
Taburia is a multivitamin and mineral fortification to provide sufficient amount of nutrient for optimal growth and development of children aged 6-59 months.
Every sachet of Taburia prepared to fulfill minimum nutrient requirements for children aged 6-59 months.
Each sachet is one gram in weight and contains vitamin A (417 mcg), B1 (0.5 mg), B2 (0.5 mg), B3 (5.0 mg), B6 (0.5 mg), B12 (1 mcg), D3 (5 mcg), E (6 mg), K (20 mcg), C (30 mcg), folic acid (150 mcg), pantothenic acid (3 mcg), Iodium (50 mcg), Iron (10 mg), Zn (5 mg) and Selenium (20 mcg).
One sachet of Taburia given to the subject by adding it to their breakfast and must be finished.
The frequency of Taburia consumption per week follows the finding of the LP analysis from the previous study.
Taburia intervention complemented by health education related to benefits, administration of Taburia, and its side effects.
Compliance will be evaluated directly by the researcher based on empty Taburia sachet and conducted every month.
|
Experimental: Optimized CF only
The intervention groups consisted of promotion of optimized complementary feeding without home fortification (taburia)
|
These programs were a process of providing information or knowledge to mother of the children consisting of information on initiation of complementary feeding, variety, and frequency of food, nutrient requirements and diet pattern for children (the amount and types of food), and benefits of Taburia.
All this information provided through class-based activities and group discussion by using leaflet and food model conducted by the researchers.
Education materials developed based on CFR models from our previous study by applying the LP approach.
There was also a demonstration on administering complementary feeding (demo and cooking class) to improve skills of the mother on food from selection, design, handling and preparing, based on requirements of the children.
This activity conducted through training once per month for the first four months of the intervention.
Components of complementary feeding promoted in this study are based on CFR using LP approach from our previous research.
|
Experimental: Taburia
The intervention groups consisted of provision taburia home fortification three sachet per week
|
Taburia is a multivitamin and mineral fortification to provide sufficient amount of nutrient for optimal growth and development of children aged 6-59 months.
Every sachet of Taburia prepared to fulfill minimum nutrient requirements for children aged 6-59 months.
Each sachet is one gram in weight and contains vitamin A (417 mcg), B1 (0.5 mg), B2 (0.5 mg), B3 (5.0 mg), B6 (0.5 mg), B12 (1 mcg), D3 (5 mcg), E (6 mg), K (20 mcg), C (30 mcg), folic acid (150 mcg), pantothenic acid (3 mcg), Iodium (50 mcg), Iron (10 mg), Zn (5 mg) and Selenium (20 mcg).
One sachet of Taburia given to the subject by adding it to their breakfast and must be finished.
The frequency of Taburia consumption per week follows the finding of the LP analysis from the previous study.
Taburia intervention complemented by health education related to benefits, administration of Taburia, and its side effects.
Compliance will be evaluated directly by the researcher based on empty Taburia sachet and conducted every month.
|
No Intervention: Control
No intervention but gave a standard education from primary health center
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from baseline nutrient intake at 6 months
Time Frame: Before intervention and after six month periode intervention
|
Data related to nutrient intake nutrient before and after the intervention measured using a 24-hour recall and a food frequency questionnaire and collected through a structured interview.
Also, data related to compliance, side effects, and acceptability of MNP home fortification (Taburia) evaluated directly by the research team during the intervention period.
Nutrient composition in-home fortification (Taburia) also includes in analysis Nutrisurvey software.
|
Before intervention and after six month periode intervention
|
Change from baseline nutrient density at 6 months
Time Frame: Before intervention and after six month periode intervention
|
Data related to nutrient density before and after the intervention measured using a 24-hour recall and a food frequency questionnaire and collected through a structured interview.
Nutrient density is calculated from intake ratio or total nutrient obtained from the diet divided by total energy from the diet per 100 kcal.
Dietary data measured using a food scale (Tanita KD-160) as well as household measurements such as glass, plate, spoon, bowl, and others.
|
Before intervention and after six month periode intervention
|
Change from baseline level of serum ferritin at 6 months
Time Frame: Before intervention and after six month period intervention
|
Serum ferritin level measured by the Enzyme-linked immunosorbent assay (ELISA) kit (Bioassay Technology Laboratory) Cat.
No. E1702Hu and expressed in units of μg/ml.
|
Before intervention and after six month period intervention
|
Change from baseline Level of zinc serum at 6 months
Time Frame: Before intervention and after six month period intervention
|
The serum zinc level measured using the GBC 933 AA type atomic absorption spectrophotometer (AAS) with a wavelength of 213.9 nm and expressed in units of μmol/L.
|
Before intervention and after six month period intervention
|
Change from baseline z-score anthropometry indices at 6 months
Time Frame: Carried out routinely every month for six months, starting at the beginning before and at the end of the intervention.
|
Weight and height of the children measured before the intervention and will be followed by regular measurement every month until the end of the intervention period.
These data analyzed using the WHO Anthro 2005 software to calculate z-score anthropometric index (weight for age, length for age, weight for height) and presented as z-score to determine the nutritional status of our samples.
Body weight measured using a digital EBSC infant weigher with the accuracy of 0.01 kg and using a standing digital weigher (CAMRY) with an accuracy of 0.01 kg for children who already can stand up.
Length or height measured using a length board (SECA 210) with an accuracy of 0.01 cm.
|
Carried out routinely every month for six months, starting at the beginning before and at the end of the intervention.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hemoglobin level
Time Frame: Measured at the end or after six month period of intervention
|
Hemoglobin level was carried out to determine the anemia status in children under five with the Flowcytometry method expressed in g/dL.
|
Measured at the end or after six month period of intervention
|
Change from baseline infection status (hs-CRP level) at 6 month
Time Frame: Before intervention and after six month period intervention
|
The hs-CRP level is an examination to measure the concentration of C-reactive protein which is more sensitive, measured by the enzyme-linked immunosorbent assay (ELISA) kit (Bioassay Technology Laboratory) Cat.
No. E1805Hu and expressed in mg/L units.
|
Before intervention and after six month period intervention
|
Gut microbiota
Time Frame: Measured at the end or after six month period of intervention
|
The relative proportion of digestive tract bacterial DNA is the relative proportion of the DNA population of Bifidobacterium and Lactobacillus spp bacteria compared to the controls analysed using the qPCR method.
|
Measured at the end or after six month period of intervention
|
Helminth status
Time Frame: Measured at the end or after six month period of intervention
|
The helminthiasis was carried out using the Kato-Katz method
|
Measured at the end or after six month period of intervention
|
Dietary diversity
Time Frame: After six month period of intervention
|
The food diversity score is calculated by summing the number of food groups consumed by individual respondents during the 24-hour recall period.
Scoring is done by giving a score of one if consuming and a score of 0 if not consuming one type of food contained in a food group that has been determined by FAO.
|
After six month period of intervention
|
Adherence to home fortification (taburia)
Time Frame: Carried out routinely every month for six months until the end of the intervention.
|
Adherence with the provision of taburia is the adherence of the mother or caregiver in giving taburia to the subject during the intervention program and is monitored directly by the researcher and field worker by collecting the number of sachets spent each month.
The provision of taburia is given once a month as many as four sachets for group optimized CF with taburia and 12 sachets for group taburia only.
|
Carried out routinely every month for six months until the end of the intervention.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Kadek T Adhi, Udayana University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2018
Primary Completion (Actual)
April 1, 2018
Study Completion (Actual)
October 31, 2018
Study Registration Dates
First Submitted
March 14, 2019
First Submitted That Met QC Criteria
March 24, 2019
First Posted (Actual)
March 27, 2019
Study Record Updates
Last Update Posted (Actual)
March 27, 2019
Last Update Submitted That Met QC Criteria
March 24, 2019
Last Verified
March 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UdayanaU_01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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