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ELICIT 2.0: Pilot Study of the Effect of Maternal Protein Supplementation During Lactation on Childhood Growth

Primary Purpose

Growth Failure, Stunting, Malnutrition

Status
Unknown status
Phase
Not Applicable
Locations
Tanzania
Study Type
Interventional
Intervention
Plumpy'Mum
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Growth Failure focused on measuring protein, breast feeding, eggs, Ready-to-eat food, infant, growth, Tanzania

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Maternal age >/= 18 years
  • Current pregnancy or infant </= 3 months

Exclusion Criteria:

  • Maternal inability to adhere to protocol
  • Multiple gestation
  • Significant birth defect
  • Maternal allergy to peanut, milk or soy
  • Lack of breast feeding at enrollment (and lack of intention to continue breast feeding at time of enrollment

Sites / Locations

  • Haydom Lutheran Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Plumpy'Mum

Arm Description

Mother/child dyads will be enrolled at child age 0-3 months and mothers will immediately begin consuming a packet of Plumpy'Mum (or similar protein food product) daily. Plumpy'Mum will be provided by the study team to the mother, who will consume this however she desires (i.e., alone or with other food). Intervention will continue for 3 months. The rational is that Plumpy'Mum consumption will improve the quality of the breast milk the child is consuming, contributing to improved growth over time. Growth will be compared to historical controls from prior studies in the area.

Outcomes

Primary Outcome Measures

Family perception of Plumpy'Mum
Families will be queried about their impression of Plumpy'Mum

Secondary Outcome Measures

Child weight-for-age Z-score (WAZ) after 3 months of Plumpy'Mum use
Child weight for WHO Z-score after 3 months of Plumpy'Mum use compared to historical controls
Child head circumference-for-age Z-score (HCZ) after 3 months of Plumpy'Mum use
Child head circumference for WHO Z-score after 3 months of Plumpy'Mum use compared to historical controls
Child mid-upper arm circumference-for-age Z-score (MUAC-Z) after 3 months of Plumpy'Mum use
Child mid-upper arm circumference Z-score after 3 months of Plumpy'Mum use compared to historical controls
Child length-for-age Z-score (LAZ) after 3 months of Plumpy'Mum use
Child length for WHO Z-score after 3 months of Plumpy'Mum use compared to historical controls
Adverse events
Number of adverse events in intervention arm, compared to historical controls
Maternal weight at 3 months
Maternal weight at 3 months compared to historical controls
Maternal mid-upper arm circumference-for-age Z-score (MUAC) at 3 months
Maternal mid-upper arm circumference at 3 months compared to historical controls

Full Information

First Posted
September 22, 2020
Last Updated
February 23, 2021
Sponsor
University of Virginia
Collaborators
Haydom Lutheran Hospital, Bill and Melinda Gates Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT04565314
Brief Title
ELICIT 2.0: Pilot Study of the Effect of Maternal Protein Supplementation During Lactation on Childhood Growth
Official Title
ELICIT 2.0: Pilot Study of the Effect of Maternal Protein Supplementation During Lactation on Childhood Growth
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
November 12, 2019 (Actual)
Primary Completion Date
March 31, 2022 (Anticipated)
Study Completion Date
August 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia
Collaborators
Haydom Lutheran Hospital, Bill and Melinda Gates Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Haydom Global Health Research Center in north central Tanzania represents an important rural setting for performing high-quality medical research in sub-Saharan Africa. The region around Haydom is agricultural (predominantly maize-based), is resource-poor and has a high degree of stunting among local infants-with 70% stunting by 18 months in the MAL-ED study and 50% in the ELICIT study (for Early Life Interventions for Childhood Growth and Development In Tanzania). While the causes of this stunting are multifactorial, a potential contributor is early-life nutritional deficiencies, including inadequate dietary protein. One likely source of low protein delivery to infants is from low intake among area mothers during lactation, with potential effects on breast milk protein content and child weight gain. The current study is a pilot study assessing our study team's ability to successfully deliver protein-containing food products (a balanced-energy protein supplement) to lactating mother is in the area and assessing whether consumption of these food products improves childhood growth in the 1st year of life. This is a pilot study because of the potential difficulties in distributing these products on a large scale for daily consumption. As such, we aim to demonstrate an effective distribution network, a means of assessing adherence, and measuring endpoints while gathering knowledge regarding community acceptance. The current pilot project will evaluate the effectiveness of distribution and adherence on approximately 100 mother/child dyads. If effective, a future project could involve a large enough sample to be powered to detect reasonable changes in linear growth. . So, while the current proposal is not adequately powered to prove a hypothesis, the hypothesis underlying the study design is that daily protein supplementation delivered as a balanced protein product (Plumpy'mum) to lactating mothers for 3 months during the period from 0-6 months post-natal life will result in an increase in infant length-for-age Z-score (LAZ) by end of treatment. LAZ will be compared to controls from prior studies in the area.
Detailed Description
In severely under-resourced areas of the world, such as the Haydom area in Tanzania (TZ), poor nutrition continues contributes to worsened health-related outcomes including growth and cognitive development. Haydom Global Health Research Center at Haydom Lutheran Hospital in north central Tanzania represents an important rural setting for performing high-quality medical research in sub-Saharan Africa. Through ongoing work in the area around Haydom in the MAL-ED and ELICIT studies, we have been attempting to improve outcomes for children in an area of severe poverty, where there is considerable malnutrition and potential sequelae: 1. Growth deficits: Poor weight gain and linear growth failure in childhood are often seen as surrogates for overall health status; persistently poor growth has implications for future work potential and lower human capital. There was a high degree of stunting in the Haydom site of Tanzanian in the multi-country observational MAL-ED study, which found that the Haydom site had the highest prevalence of stunting among all the MAL-ED sites. This degree of stunting is likely multi-factorial, though one contributor is food availability, as rates of key factors such as birthweight vary significantly according to food availability. An interim analysis of data from our ongoing ELICIT study (for Early Life Interventions for Childhood Developmental delays: Perhaps there is no more important outcome (with the exception of mortality) than the cognitive, social and emotional development of a population, with clear extensions to human capital, economic productivity and quality of life in communities. Indeed, many observational and interventional studies (including the current study) follow growth as an outcome because of its overall association with cognitive development. In MAL-ED assessments, TZ children had fewer words than seen among US children. The reasons for potential developmental delays are multifactorial, but again malnutrition may play an important role. Studies in other developing areas have demonstrated improved cognitive development following delivery of nutrition support. Nutritional Causes of Poor Growth While the causes of the stunting and developmental delays are multifactorial, a potential contributor is early-life nutritional deficiencies, including inadequate dietary protein. One likely source of low protein delivery to infants is from low intake among area mothers during lactation, with potential effects on breast milk protein content and child weight gain. Indeed, the first six months of life represents a critical phase of nutrition for the developing infant, in which all (or nearly all) nutrition is delivered through the mother's breast milk. However, it is not known whether protein supplementation during lactation in this setting would improve childhood growth and reduce stunting-or whether any improvements in growth would continue beyond the period of maternal supplementation. Assessing the potential effect of mothers receiving protein supplementation-using a balanced energy protein supplement-on childhood growth and development would require an approach that incorporates an effective distribution network, a means of assessing adherence, and a thorough knowledge of community acceptance, as well as accurate measures of endpoints on a large enough sample to be powered to detect reasonable changes in linear growth. In order to assess the feasibility of this type of approach on a smaller scale (which could be later be expanded), the current pilot project will evaluate the effectiveness of distribution and adherence on approximately 100 mother/child dyads. If this experimental approach is feasible and shows promise, it is our hope to follow it with a larger study that offers more definitive evidence of efficacy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Growth Failure, Stunting, Malnutrition, Protein Malnutrition
Keywords
protein, breast feeding, eggs, Ready-to-eat food, infant, growth, Tanzania

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Participating mothers nursing children age 0-3 months at enrollment will receive 3 months of treatment with one packet of Plumpy'Mum.
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Plumpy'Mum
Arm Type
Experimental
Arm Description
Mother/child dyads will be enrolled at child age 0-3 months and mothers will immediately begin consuming a packet of Plumpy'Mum (or similar protein food product) daily. Plumpy'Mum will be provided by the study team to the mother, who will consume this however she desires (i.e., alone or with other food). Intervention will continue for 3 months. The rational is that Plumpy'Mum consumption will improve the quality of the breast milk the child is consuming, contributing to improved growth over time. Growth will be compared to historical controls from prior studies in the area.
Intervention Type
Dietary Supplement
Intervention Name(s)
Plumpy'Mum
Intervention Description
Mothers will consume Plumpy'Mum (one packet daily) from enrollment (child age 0-3 months) for 3 months.
Primary Outcome Measure Information:
Title
Family perception of Plumpy'Mum
Description
Families will be queried about their impression of Plumpy'Mum
Time Frame
at 3 months after enrollment
Secondary Outcome Measure Information:
Title
Child weight-for-age Z-score (WAZ) after 3 months of Plumpy'Mum use
Description
Child weight for WHO Z-score after 3 months of Plumpy'Mum use compared to historical controls
Time Frame
3 months
Title
Child head circumference-for-age Z-score (HCZ) after 3 months of Plumpy'Mum use
Description
Child head circumference for WHO Z-score after 3 months of Plumpy'Mum use compared to historical controls
Time Frame
3 months
Title
Child mid-upper arm circumference-for-age Z-score (MUAC-Z) after 3 months of Plumpy'Mum use
Description
Child mid-upper arm circumference Z-score after 3 months of Plumpy'Mum use compared to historical controls
Time Frame
3 months
Title
Child length-for-age Z-score (LAZ) after 3 months of Plumpy'Mum use
Description
Child length for WHO Z-score after 3 months of Plumpy'Mum use compared to historical controls
Time Frame
3 months
Title
Adverse events
Description
Number of adverse events in intervention arm, compared to historical controls
Time Frame
3 months
Title
Maternal weight at 3 months
Description
Maternal weight at 3 months compared to historical controls
Time Frame
3 months
Title
Maternal mid-upper arm circumference-for-age Z-score (MUAC) at 3 months
Description
Maternal mid-upper arm circumference at 3 months compared to historical controls
Time Frame
12 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Maternal age >/= 18 years Current pregnancy or infant </= 3 months Exclusion Criteria: Maternal inability to adhere to protocol Multiple gestation Significant birth defect Maternal allergy to peanut, milk or soy Lack of breast feeding at enrollment (and lack of intention to continue breast feeding at time of enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark D DeBoer, MD, MSc, MCR
Organizational Affiliation
University of Virginia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Haydom Lutheran Hospital
City
Mbulu
State/Province
Manyara
Country
Tanzania

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We will assess platforms for sharing individual participant data following final data analysis.
IPD Sharing Time Frame
Within 1 year after publication of results
IPD Sharing Access Criteria
Contact PI to request

Learn more about this trial

ELICIT 2.0: Pilot Study of the Effect of Maternal Protein Supplementation During Lactation on Childhood Growth

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