Pilot Study on a Locally Prepared Food Supplement to Support Growth and Brain Health

Malnutrition Clinical Trial

Official title:

Pilot Study on a Locally Prepared Food Supplement to Support Growth and Brain Health

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03319589
• Other study ID #: 1200
• Status: Completed
• Phase: N/A
• First received: March 11, 2016
• Last updated: October 19, 2017
• Start date: March 2016
• Est. completion date: July 2016

Study information

• Verified date: October 2017
• Source: Tufts University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is a randomized controlled pilot for a future larger trial. The goals of this pilot are: a) to assess feasibility of delivering a locally prepared supplement in rural communities, and b) to generate pilot data for sample size estimates needed for a larger trial. The study will test the effect of a supplement prepared locally with local and imported ingredients on changes in standard anthropometric benchmarks of growth, cognition, immune function, hemoglobin and skin carotenoids in young children living in 2 villages in rural Guinea-Bissau. Children in the active intervention village will be compared with assessment-only controls in a separate village having comparable demographic characteristics. As part of the study, we will assess the feasibility of having local commercial bakers prepare the supplement.

Description:

Up to 20 children aged 24-30 months and 20 school children aged 6-6.5 years living in each of 2 villages in the Oio region of Guinea-Bissau (total study population up to 80, with no minimum recruitment number) will be recruited for this study, with ages documented by the official birth record, which all families possess. Villages will be a convenience sample chosen from villages within the network of our local research partner International Partnership for Human Development. Each village in this region has one school and one community health center per village, which will be involved in supplement distribution and some outcome assessments. The villages will be broadly comparable in terms of size, affluence, rates of malnutrition, the presence or absence of a school meal program, and tribal affiliation and religion.

One village will be randomly assigned to receive the locally-prepared biscuit and a daily multivitamin and the other will be randomly assigned to be an assessment-only control site. Because this is a pilot study designed to develop methodology for a future powered trial, and the logistics of local supplement preparation need to be developed in advance of the study, the randomization will occur prior to baseline testing to allow for development of infrastructure for supplement preparation. However the villagers will not be informed of the randomization until after baseline testing is complete.

Following baseline measurements of anthropometry, grip strength, cognition, non-invasive measurements of hemoglobin, and skin carotenoids, participants will receive their intervention for 12 weeks and the same measurements taken at baseline will be repeated during the last study week. Since access for the final assessment to villages may be hampered by the rainy season we also request permission to terminate the trial between 9-12 weeks of supplement consumption depending on weather conditions. Please note that cell phone access to villages is not influenced by local weather, thus communication regarding safety issues with community health workers will remain possible throughout the entire trial.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: July 2016
• Est. primary completion date: June 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 24 Months to 84 Months

Eligibility

Inclusion Criteria:

• Non-malnourished children within the 2 villages chosen for study

• Within the specified age range: 24-36 months for young children and 6-7 years for older children, who will also be enrolled in their local school. In the event that researchers cannot enroll at least 15 participants in each age range in each village, will extend the age range up to 35.99 months for young children and up to 6.99 years for older children.

• The family plans to remain in the village for the duration of the study;

• The child does not have any known food allergies as reported by the mother or guardian.

Exclusion Criteria:

• If any child is identified as malnourished at baseline, defined as a mid-upper arm circumference in the red zone of the paper tape or a weight-for-age or height-for-age z-score of less than or equal to -3.0, the child will be excluded from the study due to malnutrition, and the parents will be advised to take the child to the nearest malnutrition clinic

Related Conditions & MeSH terms

• Malnutrition

Intervention

Dietary Supplement:
• Supplement
locally prepared biscuit with low sugar content (less than 10% weight) designed to facilitate growth and cognitive development

Locations

Country	Name	City	State
United States	Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University	Boston	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
Tufts University	International Partners for Human Development

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in executive cognitive function	Two measures of executive function, working memory and task-switching abilities, will be administered through play-based games by local research team members. "Spin the Pots" and "Reverse Categorization" tasks, modeled after Carlson et al., have been age modified and culturally adopted.	Baseline and end line (12 weeks difference)
Secondary	Supplementation Attendance	community health workers will record attendance of children to consume the supplement.	Through study completion (12 weeks)
Secondary	Sicknesses	Community health workers will record sickness (malaria, stomach issues, fever) if children to consume the supplement are unwell.	Through study completion (12 weeks)
Secondary	Change in hand grip strength	. In the children aged 6-6.5 years, grip strength in both hands will be measured in duplicate using a dynamometer suitable for pediatric populations	Baseline and end line (12 weeks difference)
Secondary	Change in Hemoglobin	Hemoglobin will be measured non-invasively using a standard technique that uses light of different wavelengths directed at the finger	Baseline and end line (12 weeks difference)
Secondary	Change in skin carotenoids	a non-invasive optical measure of carotenoids in tissue, measured by shining light in the palm of the hand	Baseline and end line (12 weeks difference)
Secondary	Change in immune function	In this study we will measure delayed-type hypersensitivity (DTH) response using a standard Mantoux test composed of 3 antigens and a negative control via 4 intradermal skin injections that will be performed at baseline and the end of the study	Baseline and end line (12 weeks difference)
Secondary	Food Product Acceptability	Mothers (for the young children) and school children will be asked on a 4-point scale of '1=not at all' '2=a little', '3=moderately' and '4=very much' how much they enjoy eating the two types biscuits and the multivitamin. Preference for one biscuit over another will be determined by a higher total summed up score. The biscuit with a greater score will be used during the study.	Baseline
Secondary	Mother's Height Change	Height of the mothers measured in cm.	Baseline and end line (12 weeks difference)
Secondary	Mother's Weight Change	Weight of the mothers measured in kg.	Baseline and end line (12 weeks difference)
Secondary	Mother's MUAC change	The weight, height and MUAC of the mothers will also be measured, and family demographic data (family size, number of wives and children and ages) will be collected by questioning the mother.	Baseline and end line (12 weeks difference)
Secondary	Family Demographics Change	Family demographic data (family size, number of wives and children and ages) will be collected by questioning the mother.	Baseline and end line (12 weeks difference)
Secondary	Photographs	Parents (and children, in the case of the school children) will be asked for permission to take photographs of them that illustrate the outcome measurements and supplement consumption, for the purpose of using in presentations on the research.	through study completion, 12 weeks
Secondary	Change in weight	Multiple measurements of weight to ±0.1 kg will be taken using a calibrated digital scale	Baseline and end line (12 weeks difference)
Secondary	Change in height	Duplicate measures of height will be made with an upright stadiometer measuring to 0.1 cm	Baseline and end line (12 weeks difference)
Secondary	Change in circumferences	Duplicate measurements of mid-upper arm circumference (MUAC) will be taken at the midpoint between the acromion process of scapula and olecranon process, and head circumference will be measured in duplicate at the widest diameter, using standardized World Health Organization (WHO) methods.	Baseline and end line (12 weeks difference)
Secondary	Brain Hemoglobin	Near infrared spectroscopy	Endline at up to 12 weeks
Secondary	Brain Oxygenation	Near infrared spectroscopy	Endline at up to 12 weeks
Secondary	Brain Blood Flow	Near infrared spectroscopy	Endline at up to 12 weeks