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临床试验/NCT05166980
NCT05166980已完成不适用

Study of Multiply-fortified Salt Among Women of Reproductive Age and Preschool Children in India

University of California, San Francisco1 个研究点 分布在 1 个国家目标入组 1,389 人开始时间: 2022年10月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
1,389
试验地点
1
主要终点
Change in serum folate

研究概览

简要总结

Micronutrient (MN) deficiencies are highly prevalent in India, particularly among women of reproductive age (WRA) and preschool aged children (PSC). MN fortification of a staple food or condiment can be an effective strategy for improving the MN status of nutritionally vulnerable populations, as the approach is cost-effective, utilizes existing delivery systems, can deliver multiple MNs simultaneously, and does not require behavior change by the population. Salt is a particularly attractive vehicle for multiple MN fortification in India, as it is universally consumed in fairly consistent amounts; and 93% of households already use adequately iodized salt.

The overall goal of this study is to evaluate the nutritional impact of quintuply-fortified salt with iron in the form of FePP (FePP-Q5S, i.e. salt fortified with iron in the form of ferric pyrophosphate plus ethylenediaminetetraacetic acid as an enhancer of absorption; zinc in the form of zinc oxide; vitamin B12; folic acid; and iodine) vs. quintuply-fortified salt with iron in the form of eFF (eFF-Q5S i.e. salt fortified with iron in the form of encapsulated ferrous fumarate; zinc in the form of zinc oxide, vitamin B12, folic acid, and iodine) vs. iodized salt (IS) for the improvement of micronutrient status among nonpregnant WRA and preschool-aged children (12-59 months of age) in Punjab, India.

Enrolled women (and their affiliated households) will be randomized to receive 1 kg of their assigned study salt per month for 12 months, and will be instructed to use the study salt in place of their usual salt. Blood and urine samples will be collected from participant WRA and PSC at enrollment, 6 months and at the end of the 12-month intervention period. The change in the mean concentration of various MN biomarkers will be considered primary outcomes. Stool samples will also be collected from a subgroup of women and children to assess changes in the gut microbiome over the intervention period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

Study salts will be packaged in color-coded, polyethylene bags.

入排标准

年龄范围
12 Months 至 49 Years(Child, Adult)
性别
All
接受健康志愿者
是

入选标准

  • •for women of reproductive age:
  • •18-49 years of age;
  • •Not currently pregnant (self-reported);
  • •Not severely anemia (defined as a hemoglobin concentration < 8 g/dL);
  • •Not planning to become pregnant within the next year;
  • •Permanent resident of the study village with no plans to move or travel outside the village for more than 4 weeks over the next 12 months;
  • •No serious health problems that requires regular visits to a health facility;
  • •Willingness to use refined salt provided by the study as a primary source of household discretionary salt.

排除标准

  • •for women of reproductive age:
  • •Age <18 or > 49 years of age;
  • •Pregnant at the time of enrollment (self report) or planning to become pregnant within the next year;
  • •Severely anemic (i.e. hemoglobin concentration < 8 g/dL);
  • •Not a permanent resident of the study area;
  • •Planning to leave the study area for at least one month over the study period;
  • •Serious health problem that interferes with eating practices and/or requires hospitalization;
  • •Unwilling to use refined salt provided by the study as the primary source of the household's discretionary salt.
  • •Inclusion criteria for preschool children:
  • •Child 12-59 months of age at the time of enrollment;
  • •Child's mother or primary female caregiver has been enrolled into the parent trial;
  • •Not severely anemic (defined as a hemoglobin concentration < 7 g/dL);
  • •Child's family is a permanent resident of the study village with no plans to move or travel outside the village for more than 4 weeks over the next 12 months;
  • •No serious medical problems that interfere with the child's eating practices;
  • •Child's mother or primary female caregiver is willing to use refined salt provided by the study as the primary source of the household's discretionary salt for the course of the study.
  • •Exclusion criteria for preschool children:
  • •Child age < 12 or > 59 months of age;
  • •Child's mother has not been enrolled in the parent trial;
  • •Severely anemic (i.e. hemoglobin concentration < 7 g/dL);
  • •Child's family is not a permanent resident of the study village and/or has plans to travel outside the village for more than 4 weeks over the next 12 months;
  • •Serious health problem that interferes with the child's eating practices;
  • •Child's mother or primary female caregiver is unwilling to use refined salt provided by the study as the primary sources of the household's discretionary salt for the course of the study.

研究组 & 干预措施

FePP-Q5S

Experimental

Salt fortified with iron in the form of ferric pyrophosphate (at 1.3 mg of iron per gram of salt) plus ethylenediaminetetraacetic acid (EDTA) as an enhancer of absorption, zinc in the form of zinc oxide (at 1.4 mg of zinc per gram of salt), vitamin B12 (at 0.6 ug of vitamin B12 per gram of salt), folic acid (at 52 ug per gram of salt) and iodine (at 30 mg of iodine per gram of salt). Mean intake of discretionary salt among women of reproductive age in the study area is 4.6 grams per day. Therefore, the FePP-Q5S will deliver an average of 6.0 mg of iron, 6.4 mg of zinc, 2.8 ug of vitamin B12, 241 ug of folic acid, and 138 mg of iodine to each participating woman per day.

干预措施: Mutiply-fortified salt (Dietary Supplement)

eFF-Q5S

Experimental

Salt fortified with iron in the form of encapsulated ferrous fumarate (at 1.3 mg of iron per gram of salt), zinc in the form of zinc oxide (at 1.4 mg of zinc per gram of salt), vitamin B12 (at 0.6 ug of vitamin B12 per gram of salt), folic acid (at 52 ug per gram of salt) and iodine (at 30 mg of iodine per gram of salt). Mean intake of discretionary salt among women of reproductive age in the study area is 4.6 grams per day. Therefore, the eFF-Q5S will deliver an average of 6.0 mg of iron, 6.4 mg of zinc, 2.8 ug of vitamin B12, 241 ug of folic acid, and 138 mg of iodine to each participating woman per day.

干预措施: Mutiply-fortified salt (Dietary Supplement)

Iodized Salt

Active Comparator

Iodized salt containing 30 mg of iodine per gram of salt. Mean intake of discretionary salt among women of reproductive age in the study area is 4.6 grams per day. Therefore, the iodized salt will deliver an average of 138 mg of iodine to each participating woman per day.

干预措施: Iodized salt (Dietary Supplement)

结局指标

主要结局

Change in serum folate

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in mean serum folate concentration

Change in urinary iodine

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in mean urinary iodine concentration

Change in serum vitamin B12

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in mean serum vitamin B12 concentration

Change in methylmalonic acid

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in mean concentration of methylmalonic acid

Change in plasma zinc

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in mean plasma zinc concentration

Change in serum ferritin

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in inflammation-adjusted mean serum ferritin concentration

Change in soluble transferrin

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in inflammation-adjusted mean soluble transferrin concentration

Change in holo-transcobalamin

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in mean holo-transcobalamin concentration

Change in serum thyroglobulin

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in mean serum thyroglobulin concentration

Change in hemoglobin

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in mean hemoglobin concentration

Change in red blood cell folate

时间窗: Enrollment to 12 months (i.e. end of intervention period)

Change in mean red blood cell folate concentration

次要结局

  • Change in gut microbiota(Enrollment to 12 months (i.e. end of intervention period))
  • Change in nail zinc(Enrollment to 12 months (i.e. end of intervention period))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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