Can text messages fight anemia? new trial tests digital nutrition for teens
NCT ID NCT07493772
First seen Jun 27, 2026 · Last updated Sep 18, 2026 · Updated 3 times
Summary
This study tests whether adding digital nutrition education—via SMS or group sessions—to daily micronutrient supplements can lower anemia rates in 1,200 adolescents aged 15-19 in Dar es Salaam, Tanzania. All participants get supplements and basic nutrition info; some also receive weekly texts or in-person digital group sessions. The goal is to see if these extra nudges improve supplement use and reduce anemia over 9 months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- multiple micronutrient supplements (MMS) and digital nutrition education (SMS/WhatsApp messages and group sessions)
- What this could lead to
- If successful, this approach could offer a low-cost, scalable way to reduce anemia and improve nutrition among adolescents in low-resource settings.
- What could go wrong
- This is a behavioral intervention trial, not a drug test. Results may be limited by adherence to supplements or engagement with digital messages, and may not apply outside Tanzania.
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 1,200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2027
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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15 to 19 years
- 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: * Aged 15-19 years at enrollment. * Resident in the Dar es Salaam HDSS coverage area. * Has access to at least one phone (own or shared within the household; feature phone or smartphone). * Demonstrates basic literacy skills sufficient to understand simple written messages. * Has capacity to provide informed consent (for those ≥18 years) or assent (for those \<18 years, with parental/guardian consent). Exclusion Criteria: * Currently pregnant. * Enrolled in the ARISE-NUTRINT trial. * Currently taking iron and folic acid or multiple micronutrient tablets for anemia outside this study. * Known to have HIV infection at the time of screening. * More than one eligible adolescent per household: if multiple adolescents meet criteria in a household, one will be randomly selected to participate.
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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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Dar Health and Demographic Surveillance System Area
Dar es Salaam, Tanzania
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