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| ID | Type | Description | Link |
|---|---|---|---|
| 112NECHR | Other Identifier | National Ethics Committee for Health Research, Cambodia |
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| Name | Class |
|---|---|
| Sackler Institute for Nutrition Science | OTHER |
| Bill and Melinda Gates Foundation | OTHER |
| Helen Keller International | OTHER |
| NCHADS - Ministry of Health of Cambodia |
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Beriberi is a potentially fatal disease caused by vitamin B1 (thiamine) deficiency that still occurs in Southeast Asia despite near eradication elsewhere. Mothers with a diet low in thiamine produce thiamine-poor milk, putting their infants at a high risk of developing thiamine deficiency and beriberi. There is also a growing body of evidence suggesting thiamine deficiency not severe enough to cause clinical symptoms may negatively effect cognitive development and functioning of the infant. Since human milk should be the sole source of nutrition for babies during the first six months, maternal thiamine intake must be improved to combat this disease.
The investigators' recent study of thiamine-fortified fish sauce in Cambodia showed that fortification could increase maternal and infant thiamine status'. However, centrally produced fish sauce may not reach the poorest communities who make their own fish sauce, and fish sauce is not consumed in all regions where we find thiamine deficiency. Salt, by contrast, is a common condiment in most regions of the world and has proven to be a successful global fortification vehicle for iodine.
Suboptimal maternal thiamine intake puts exclusively breastfed infants at risk of low thiamine status, impaired cognitive development, and infantile beriberi, which can be fatal. Thiamine fortification of salt is a potentially low-cost and sustainable means of combating suboptimal thiamine status; however knowledge gaps must be filled before thiamine fortification can proceed. In this study, mothers will consume thiamine supplements in order to model the thiamine dose required to optimize human milk thiamine concentrations for the prevention of beriberi. Other thiamine biomarkers will be assessed, and usual salt intake will be measured. Finally, the investigators will assess the effects of early-life thiamine exposure on infant neuro-cognitive development.
(see full protocol)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Negative Control | Placebo Comparator | placebo; 0 mg thiamine |
|
| EAR Group | Experimental | 1.2 mg thiamine as thiamine hydrochloride |
|
| Double EAR Group | Experimental | 2.4 mg thiamine as thiamine hydrochloride |
|
| Positive Control | Experimental | 10 mg thiamine as thiamine hydrochloride |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| thiamine (as thiamine hydrochloride) | Dietary Supplement | Opaque capsules containing varying amounts of thiamine hydrochloride and cellulose filler. All thiamine is delivered as thiamine hydrochloride, calculated using a 1.271 correction factor (ratio of molecular weights of thiamine hydrochloride and thiamine). |
| Measure | Description | Time Frame |
|---|---|---|
| Human milk total thiamine concentration | To estimate the dose on the dose response curve where additional maternal intake of thiamine (oral dose) no longer meaningfully increases human milk total thiamine concentration at 24 weeks postpartum. | 24 weeks postpartum |
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| Measure | Description | Time Frame |
|---|---|---|
| Infant thiamine diphosphate concentrations (ThDP) | To estimate the dose on the dose response curve where additional maternal intake of thiamine (oral dose) no longer meaningfully increases infant thiamine diphosphate concentrations (ThDP) 24 weeks postnatally, and assess whether this depends on the presence/absence of a genetic hemoglobin disorder. | 24 weeks postnatal |
Inclusion Criteria:
Mothers of a newborn who:
Exclusion Criteria:
Mothers of a newborn who:
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| Name | Affiliation | Role |
|---|---|---|
| Kyly C Whitfield, PhD | Mount Saint Vincent University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Helen Keller International | Kampong Thom | Kapmong Thom Province | Cambodia |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 39699595 | Derived | Baldwin DA, Measelle J, Gallivan L, Sanchirico A, Weinstein N, Bala A, Chan K, Gallant J, Borath M, Kroeun H, Wieringa FT, Green TJ, Whitfield KC. Language processing in breastfed infants at risk of thiamine deficiency benefits from maternal thiamine supplementation. Dev Psychol. 2025 Aug;61(8):1427-1440. doi: 10.1037/dev0001829. Epub 2024 Dec 19. | |
| 33829271 |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Aug 14, 2019 | Sep 20, 2019 | Prot_SAP_001.pdf |
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| ID | Term |
|---|---|
| D013832 | Thiamine Deficiency |
| ID | Term |
|---|---|
| D014804 | Vitamin B Deficiency |
| D001361 | Avitaminosis |
| D003677 | Deficiency Diseases |
| D044342 | Malnutrition |
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| ID | Term |
|---|---|
| D013831 | Thiamine |
| ID | Term |
|---|---|
| D013844 | Thiazoles |
| D013457 | Sulfur Compounds |
| D009930 | Organic Chemicals |
| D001393 | Azoles |
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| OTHER |
| Ministry of Planning, Cambodia | UNKNOWN |
| South Australian Health and Medical Research Institute | OTHER |
| Institut de Recherche pour le Developpement | OTHER_GOV |
| University of Oregon | OTHER |
Randomized placebo controlled, double-blinded, four-parallel arm, multicentre trial
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double-blinded
|
| Human milk total thiamine concentrations | To estimate the dose on the dose response curve where additional maternal intake of thiamine (oral dose) no longer meaningfully increases human milk total thiamine concentration at 4 and 12 weeks postpartum. | 4 and 12 weeks postpartum |
| Infant transketolase activity | To estimate the dose on the dose response curve where additional maternal intake of thiamine (oral dose) no longer meaningfully increases infant transketolase activity at 24 weeks postnatally, and assess whether this depends on the presence/absence of a genetic hemoglobin disorder. | 24 weeks postnatal |
| Maternal ThDP (dose response) | To estimate the dose on the dose response curve where additional maternal intake of thiamine (oral dose) no longer meaningfully increases maternal ThDP at 24 weeks postpartum, and assess whether this depends on the presence/absence of a genetic hemoglobin disorder. | 24 weeks postpartum |
| Maternal transketolase activity (dose response) | To estimate the dose on the dose response curve where additional maternal intake of thiamine (oral dose) no longer meaningfully increases maternal ETKac at 24 weeks postpartum, and assess whether this depends on the presence/absence of a genetic hemoglobin disorder. | 24 weeks postpartum |
| Human milk total thiamine concentrations | To test for differences between the 4 randomized groups on human milk total thiamine at 4, 12, and 24 weeks postpartum. | 4, 12, and 24 weeks postpartum |
| Maternal ThDP (by arm) | To test for differences between the 4 randomized groups on maternal ThDP at 24 weeks postpartum, and assess whether this depends on the presence/absence of genetic hemoglobin disorder. | 24 weeks postpartum |
| Maternal transketolase activity (by arm) | To test for differences between the 4 randomized groups on maternal ETKac at 24 weeks postpartum and assess whether this depends on the presence/absence of a genetic hemoglobin disorder. | 24 weeks postpartum |
| Household salt intake | To estimate usual household salt intake from mean fortnightly salt disappearance (weight lost, in g). | within 2 and 24 weeks postpartum |
| Salt intake of household members | To estimate salt intake among a subset of 100 lactating women, their male partners (if applicable), and their children 24-59 months (if applicable) using observed weighed salt intake records. | within 2 and 24 weeks postpartum |
| Sodium intake of women | To estimate sodium intake using 24 hr urinary sodium concentrations among a subset of 100 lactating women. | within 2 and 24 weeks postpartum |
| Mullen scores | To test for differences between the 0 & 10 mg randomized groups on Composite Mullen and the 5 subscales of the Mullen at 24 and 52 weeks postnatally. Score notes for Mullen Scales of Early Learning Gross Motor Scale: Raw score range: 0-36 (higher scores reflect better performance) Visual Reception Scale: Raw score range: 0-50 (higher scores reflect better performance) Fine Motor Scale: Raw score range: 0-49 (higher scores reflect better performance) Receptive Language Scale: Raw score range: 0-48 (higher scores reflect better performance) Expressive Language Scale: Raw score range: 0-50 (higher scores reflect better performance) All raw scores are converted to age-adjusted T-scores (provided by manual). An optional Early Learning Composite Score can be calculated by summing the T-scores of all but the Gross Motor Scale. | 24 and 52 weeks postnatal |
| Visual paired comparison | To test for differences between the 0 & 10 mg randomized groups on Visual Paired Comparison Novelty Score and the attention and processing speed subscales at 24 and 52 weeks postnatally. Score notes for Visual Paired Comparison task Scale ranges: An overall novelty score is calculated that averages across all face and pattern trials, and is a percentage reflecting the percent of time infants' looked at the novel item during the test phase, calculated as the duration looking to the novel item divided by the sum of the duration of looking to the novel item plus the duration looking to the familiar item. Sub-scales: Two sub-scales are calculated: the novelty score averaged across face trials, and the novelty score averaged across pattern trials. The total scale composite averages the novelty score across the two sub-scales. For all scales, he range is 0-100%, and higher novelty scores indicate better outcomes. | 24 and 52 weeks postnatal |
| Language Preference Task | To test for differences between the 0 & 10 mg randomized groups on the Language Preference Task Score at 24 weeks postnatally. | 24 weeks postnatal |
| Oculomotor scores | To test for differences between 0 & 10 mg randomized groups on oculomotor scores at 24 weeks postnatally. Score notes for the Oculomotor Test: The proposed oculomotor test is not a single, published instrument, but instead, combines several standard screening items. Strabismus: absent or present; score: 0-1 Nystagmus: absent or present; score: 0-1 Amblyopia: absent or present; score 0-1 Saccade:
Smooth pursuit:
Total oculomotor score (optional): sum of all scored exam items: range 0-9 | 24 weeks postnatal |
| Inflammation | To determine the effect of inflammation, as measured by C-reactive protein (CRP) and α-1-acid-glycoprotein (AGP) on maternal ThDP at 2 and 24 weeks postpartum, and infant ThDP at 24 weeks postnatal. | 24 weeks postnatal |
| Gallant J, Chan K, Green TJ, Wieringa FT, Leemaqz S, Ngik R, Measelle JR, Baldwin DA, Borath M, Sophonneary P, Yelland LN, Hampel D, Shahab-Ferdows S, Allen LH, Jones KS, Koulman A, Parkington DA, Meadows SR, Kroeun H, Whitfield KC. Low-dose thiamine supplementation of lactating Cambodian mothers improves human milk thiamine concentrations: a randomized controlled trial. Am J Clin Nutr. 2021 Jul 1;114(1):90-100. doi: 10.1093/ajcn/nqab052. |
| 31292183 | Derived | Whitfield KC, Kroeun H, Green T, Wieringa FT, Borath M, Sophonneary P, Measelle JR, Baldwin D, Yelland LN, Leemaqz S, Chan K, Gallant J. Thiamine dose response in human milk with supplementation among lactating women in Cambodia: study protocol for a double-blind, four-parallel arm randomised controlled trial. BMJ Open. 2019 Jul 9;9(7):e029255. doi: 10.1136/bmjopen-2019-029255. |
| D009748 |
| Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
| D006573 |
| Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D011743 | Pyrimidines |