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Child MalnutritionNCT02257437

Acceptability of a Multiple Micronutrient-Fortified Lipid-Based Nutrient Supplement for Children Under Two in Cambodia

A study testing LNS snack, Corn-soy blend ++ (CSB++) and Sprinkles in people with Child Malnutrition, run by Institut de Recherche pour le Developpement, Cambodia at 1 site in Cambodia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this trial is to evaluate the acceptability of the LNS to women and their children aged 12-17 months in comparison to Corn Soy Blend++, and Sprinkles added to borbor (white rice porridge, which is the traditional weaning food in Cambodia). Read more about this study

Who is it for?
Ages 9 to 23 monthsHealthy volunteers can take part
Conditions the study is for
Child Malnutrition
What is being tested?
LNS snack, Corn-soy blend ++ (CSB++) and Sprinkles
Could I receive a placebo?
No, everyone receives an active treatment
How many people
92 participants
Where
1 siteCambodia
Study dates
Jun 2015to Jul 2015
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 9 to 23 months
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Children aged 9-23 months and their caregivers
  • Have been eating solids for at least three months
  • Singletons
  • Normally nourished or only moderately malnourished (MUAC >115mm, WHZ score >-3)
  • Healthy (no ill-health in past three days)
  • No known food intolerances
Show all 9Show fewer
  • Have not been using Sprinkles, CSB++ or similar supplementary foods or supplements
  • Informed signed consent of mother
  • Mothers are healthy

Who cannot join

  • Children <9 months or >23mths
  • Not yet eating solid food for at least three months
  • Twins/multiples
  • Severely malnourished (MUAC< 115mm, WHZ score<3, bipedal pitting oedema).
  • Oedema and/or any medical complications at recruitment or illness requiring referral, or any ill health in past three days.
  • Known intolerances
Show all 9Show fewer
  • Children enrolled in Sprinkles, CSB++ or similar program
  • No informed signed consent of caregiver
  • Medical complications or illness requiring referral at time of recruitment or previous two weeks

Trial locations and contacts

1 site in 1 country.

Cambodia1 site
  • IRD Cambodia

    Phnom Penh

Other trials in Cambodia

About this study

Official title: Acceptability of a Locally-Produced Multiple Micronutrient-Fortified Lipid-Based Nutrient Supplement (LNS) for Children Under Two Years in Cambodia

The purpose of this trial is to evaluate the acceptability of the LNS to women and their children aged 12-17 months in comparison to Corn Soy Blend++, and Sprinkles added to borbor (white rice porridge, which is the traditional weaning food in Cambodia). Acceptability will be assessed through a sensory test for caregivers, and by measuring children's consumption.

Read the detailed description

BACKGROUND:

In Cambodia, progress in combatting malnutrition has stalled. In 2010, 40% of all children under five (and 49% of 4-5 year-olds) were stunted, 11% were wasted, and 28% were underweight, indicating, respectively, chronic and acute malnutrition, and a combination of the two. Stunting is partially attributed to poor complementary feeding, which remains inadequate for achieving growth outcomes and micronutrient status.

Malnutrition can be prevented and treated with supplementary foods. These foods usually contain a source of protein and lipids such as powered milk, soy or peanuts, and multiple micronutrients. They can be prepared as a fortified blended product, such as Corn-Soy Blend++ (CSB++), that is mixed with water to make a porridge, or ready-to-use supplementary foods (RUSFs). The latter are usually lipid-based nutrient supplements (LNSs) which are often pastes such as the peanut-based Plumpy'Nut™. These energy-dense supplementary foods contain both macro and micronutrients and are used to prevent and treat malnutrition by promoting improved linear growth, weight gain and micronutrient status among children. Until recently, prevention of malnutrition has relied on fortified blended products. The new RUSFs are also proving effective, as they are higher energy and have a longer shelf life, and since they require no preparation, are convenient. Another common nutrition intervention is multiple micronutrient supplements such as Sprinkles. These are individually-packed powders that can be added to food. However, micronutrients are more likely to achieve growth outcomes when they are combined with energy, for example, in lipid-based nutrient supplements and there is no evidence that micronutrient powders alone contribute to growth.

Until June 2014, the United Nations World Food Program (WFP) used CSB++ (now called Supercereal Plus) to prevent malnutrition in Cambodia. Sprinkles are also being distributed, though not widely, to prevent micronutrient deficiencies. These products that have been recently or are currently used are relatively expensive to procure and ship to Cambodia and in the case of Sprinkles, are not as effective as foods that contain macronutrients. Moreover, CSB++ was not very well accepted in practice, and WFP has phased it out. Therefore, UNICEF and the Cambodian Ministry of Health are looking for a locally-produced product containing macro and micronutrients to prevent malnutrition in Cambodia. Locally-produced products are more likely to be acceptable and cheaper than imported products.

Regardless of how effective a product may be, it is vital to determine its acceptability in a given setting, in other words, will a child eat the product and will a caregiver feed it to them. Acceptability to children can be measured by how much they eat and how readily, while acceptability to caregivers is measured in terms of their sensory perception of the food, that is, of the smell, colour, and taste.

TRIAL DESIGN AND METHODOLOGY:

Therefore, this trial will evaluate the acceptability of the LNS to women and their children aged 9-23 months in comparison to CSB++, Sprinkles added to borbor.

The trial is a cluster randomised, incomplete block, 4 x 4 crossover design that aims to establish the superiority (i.e. the greater acceptability) of the novel LNS (as a snack or mixed with borbor), in comparison to CSB++, and Sprinkles added to borbor. The allocation ratio is 1:1. The study will take place in two parts over two weeks:

  1. Substudy 1: Acceptability by children, three days x four foods for a total of 12 days
  2. Substudy 2: Acceptability by mothers, 13th day

The study will be conducted in peri-urban Phnom Penh. The study will be conducted in four test-feeding sites such as pagodas or health centres. Participants will be recruited for convenience from villages close to the four sites. The four test-feeding sites will be randomly allocated to begin on one of the foods. All children in a given site will be eating the same food at the same time for three consecutive days.

Upon consent and enrolment, baseline data will be collected from the participants. This will include demographics, morbidity, anthropometry (weight, height, mid-upper arm circumference), and dietary data (breastfeeding, food frequency and dietary diversity).

Mothers will be asked to bring their child to their designated test-feeding site for the following 12 days. They will be asked not to feed their child for the preceding hour, if possible. The same food will be given three days in a row, to allow averaging of results and reduce the effect of chance findings.

Children will receive the four foods, namely, the LNS added to borbor, CSB++ porridge, Sprinkles added to borbor, and the LNS snack, for three days each over twelve days. Children in each group will taste each food in a different sequence (to balance for carry-over effects). The mothers will be asked to feed their child for 15 minutes or until the child refuses to eat any more. The amount of food consumed will be measured each time the child eats. Each mother will be asked to assess how she thinks her child liked the food, taking into account the amount eaten and the child's reactions and emotional state during feeding.

On the 13th day, mothers will be asked to come to the test-feeding site, alone if possible, to rank the foods. For the sensory test, the foods will be presented one at a time. No weighing is necessary and mothers will not be expected to eat a whole cup. Between foods, the mother will be asked to rinse her mouth out with water. Mothers will rate each food with respect to colour, smell, taste, preparation process, and their overall opinion. The foods will then be presented at the same time and mothers will then be asked to rank them. Finally, on the 14th day, a smaller number of mothers (8-12) from each site will be asked to stay for a focus group discussion related to infant feeding practices and reasons for preference ranking.

Being tested
LNS snack, Corn-soy blend ++ (CSB++), Sprinkles, LNS + borbor
Keywords
Ready-to-use supplementary food (RUSF), Lipid-based nutrient supplement (LNS), Multiple micronutrients (MMN), Complementary feeding, Home fortification, Acceptability, Infant and young child feeding (IYCF), Cambodia, Cross-over studies
Medical subject headings
Child Nutrition Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • LNS snackDietary supplement

    Compact, paste-filled wafer snack containing fish, rice, soy, mungbeans, oil, sugar and multiple micronutrients.

  • Corn-soy blend ++ (CSB++)Dietary supplement

    Also called Supercereal Plus

    Blended flour containing soy, corn, milk powder, oil, sugar and multiple micronutrients.

  • SprinklesDietary supplement

    Multiple micronutrient powder packaged in sachet added to borbor (traditional white rice porridge).

  • LNS + borborDietary supplement

    Compact, paste-filled wafer snack containing fish, rice, soy, mungbeans, oil, sugar and multiple micronutrients added to borbor (traditional white rice porridge).

Study groups in NCT02257437
Study groupRoleWhat they receive
LNS + borborExperimentalLipid-based nutrient supplement (LNS) added to borbor
Receives: Dietary Supplement: LNS snack; Dietary Supplement: Corn-soy blend ++ (CSB++); Dietary Supplement: Sprinkles; Dietary Supplement: LNS + borbor
Corn-soy blend ++ (CSB++)Active comparatorCSB++ porridge
Receives: Dietary Supplement: LNS snack; Dietary Supplement: Corn-soy blend ++ (CSB++); Dietary Supplement: Sprinkles; Dietary Supplement: LNS + borbor
SprinklesActive comparatorSprinkles added to borbor
Receives: Dietary Supplement: LNS snack; Dietary Supplement: Corn-soy blend ++ (CSB++); Dietary Supplement: Sprinkles; Dietary Supplement: LNS + borbor
LNS snackActive comparatorLNS eaten as snack
Receives: Dietary Supplement: LNS snack; Dietary Supplement: Corn-soy blend ++ (CSB++); Dietary Supplement: Sprinkles; Dietary Supplement: LNS + borbor

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Child's consumption

    How much of a given food the children consume

    Measured: Within 15 minutes

Secondary outcomes (2)
  1. Child's preference

    Mothers' assessment of their child's ranked preference for the food

    Measured: 3 days

  2. Mother's ranking

    Mother's ranked preference for the food

    Measured: 1 session

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Oct 2014 (estimated)
  2. Study startJun 2015
  3. Primary completionJul 2015
  4. Study completionJul 2015

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
92 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02257437
Sponsor's protocol ID
LNS-CAMB-INFANTS
Status last verified
Sep 2016
First submitted
2 Oct 2014
Last updated
15 Sep 2016
Results posted
No
Data monitoring committee
No

Publications

  • Borg B, Mihrshahi S, Griffin M, Chamnan C, Laillou A, Wieringa FT. Crossover trial to test the acceptability of a locally produced lipid-based nutrient supplement (LNS) for children under 2 years in Cambodia: a study protocol. BMJ Open. 2017 Sep 6;7(9):e015958. doi: 10.1136/bmjopen-2017-015958.

    PubMed 28882910

Questions about this trial

What is this clinical trial studying?

A study testing LNS snack, Corn-soy blend ++ (CSB++) and Sprinkles in people with Child Malnutrition, run by Institut de Recherche pour le Developpement, Cambodia at 1 site in Cambodia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Sep 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Cambodia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Child's consumption (time frame: Within 15 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02257437, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Sep 2016.

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