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Could a simple packaging change help more children get the nutrients they need?
NCT ID NCT07129109
First seen Jul 10, 2026 · Last updated Jul 10, 2026
Summary
This study tests whether giving caregivers a weekly bulk container (7-day supply) versus daily single-use sachets (1-day supply) of a nutrient supplement improves how much children actually consume. About 500 caregivers of children aged 6-24 months in northern Ghana will try both packaging types for one month each. Researchers will measure adherence and ease of use to guide future nutrition programs.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- small-quantity lipid-based nutrient supplements (SQ-LNS)
- What this could lead to
- If one packaging format works better, it could make it easier for caregivers to give children the full dose, helping reduce malnutrition more effectively in low-resource settings.
- What could go wrong
- This is a small implementation study focused on packaging, not a test of the supplement itself. Results may not apply to other regions or programs.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 505 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Primary caregiver of a child aged 6-24 months attending growth monitoring and promotion (GMP) services at one of the participating health facilities * Willing and able to provide informed consent * Plans to remain in the area for the duration of the study period * Agrees to participate in surveys and/or interviews related to supplement use Exclusion Criteria: * Caregiver of a child with a diagnosed severe illness requiring hospitalization * Caregiver under the age of 18
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Sixteen health facilities in the Northern Region of Ghana (exact sites TBD)
Tamale, Ghana
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