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.
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.
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:
- Substudy 1: Acceptability by children, three days x four foods for a total of 12 days
- 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.
- Conditions
- Child Malnutrition
- 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 group | Role | What they receive |
|---|---|---|
| LNS + borbor | Experimental | Lipid-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 comparator | CSB++ porridge Receives: Dietary Supplement: LNS snack; Dietary Supplement: Corn-soy blend ++ (CSB++); Dietary Supplement: Sprinkles; Dietary Supplement: LNS + borbor |
| Sprinkles | Active comparator | Sprinkles added to borbor Receives: Dietary Supplement: LNS snack; Dietary Supplement: Corn-soy blend ++ (CSB++); Dietary Supplement: Sprinkles; Dietary Supplement: LNS + borbor |
| LNS snack | Active comparator | LNS 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.
Child's consumption
How much of a given food the children consume
Measured: Within 15 minutes
Secondary outcomes (2)
Child's preference
Mothers' assessment of their child's ranked preference for the food
Measured: 3 days
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.
- First posted6 Oct 2014 (estimated)
- Study startJun 2015
- Primary completionJul 2015
- Study completionJul 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Child MalnutritionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Institut de Recherche pour le Developpement, Cambodia
- Sponsor type
- Other government
- Collaborators
- UNICEF, Department of Fisheries Post-harvest Technologies and Quality Control
- Responsible party
- Principal investigator, Bindi Borg, University of Sydney
- Investigators
- Frank T Wieringa, MD, PhD, Study director, IRDBindi Borg, PhD student, Principal investigator, University of Sydney
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
Study at a glance
From the registry record, last updated by the sponsor on 15 Sep 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Acceptability of a Locally-Produced Multiple Micronutrient-Fortified Lipid-Based Nutrient Supplement (LNS) for Children Under Two Years in Cambodia
- ClinicalTrials.gov ID
- NCT02257437
- Acronym / sponsor ID
- LNS-CAMB-INFANTS
- Conditions
- Child Malnutrition
- 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
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 92 participants (actual)
- Lead sponsor
- Institut de Recherche pour le Developpement, CambodiaOther government
- Collaborators
- UNICEF, Department of Fisheries Post-harvest Technologies and Quality Control
- Study start
- Jun 2015
- Primary completion
- Jul 2015 (actual)
- Study completion
- Jul 2015 (actual)
- First posted
- 6 Oct 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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:
- Substudy 1: Acceptability by children, three days x four foods for a total of 12 days
- 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.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| LNS + borbor | Experimental | Dietary Supplement: LNS snack, Dietary Supplement: Corn-soy blend ++ (CSB++), Dietary Supplement: Sprinkles, Dietary Supplement: LNS + borborLipid-based nutrient supplement (LNS) added to borbor |
| Corn-soy blend ++ (CSB++) | Active comparator | Dietary Supplement: LNS snack, Dietary Supplement: Corn-soy blend ++ (CSB++), Dietary Supplement: Sprinkles, Dietary Supplement: LNS + borborCSB++ porridge |
| Sprinkles | Active comparator | Dietary Supplement: LNS snack, Dietary Supplement: Corn-soy blend ++ (CSB++), Dietary Supplement: Sprinkles, Dietary Supplement: LNS + borborSprinkles added to borbor |
| LNS snack | Active comparator | Dietary Supplement: LNS snack, Dietary Supplement: Corn-soy blend ++ (CSB++), Dietary Supplement: Sprinkles, Dietary Supplement: LNS + borborLNS eaten as snack |
Who may qualify
- Ages
- 9 to 23 months
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (9 listed)
- 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)
Key exclusion criteria (9 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| LNS snackCompact, paste-filled wafer snack containing fish, rice, soy, mungbeans, oil, sugar and multiple micronutrients. | Dietary supplement | Corn-soy blend ++ (CSB++), LNS + borbor, LNS snack, Sprinkles |
| Corn-soy blend ++ (CSB++)Also: Supercereal PlusBlended flour containing soy, corn, milk powder, oil, sugar and multiple micronutrients. | Dietary supplement | Corn-soy blend ++ (CSB++), LNS + borbor, LNS snack, Sprinkles |
| SprinklesMultiple micronutrient powder packaged in sachet added to borbor (traditional white rice porridge). | Dietary supplement | Corn-soy blend ++ (CSB++), LNS + borbor, LNS snack, Sprinkles |
| LNS + borborCompact, paste-filled wafer snack containing fish, rice, soy, mungbeans, oil, sugar and multiple micronutrients added to borbor (traditional white rice porridge). | Dietary supplement | Corn-soy blend ++ (CSB++), LNS + borbor, LNS snack, Sprinkles |
Primary outcome
Child's consumption
Time frame: Within 15 minutes
How much of a given food the children consume
2 secondary outcomes
Child's preference
Time frame: 3 days
Mother's ranking
Time frame: 1 session
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Sep 2016.
- Derived from this study: PubMed 28882910Borg 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Frank T Wieringa, MD, PhD study director
IRD
Bindi Borg, PhD student principal investigator
University of Sydney
1 site in 1 country: see every site and its status.
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.