CompletedNot Applicable

Mobile Messaging for Improved Nutrition

Senegal488 participantsStarted 2022-06-10

Plain-language summary

This project will examine the impact of an infant and young child feeding (IYCF) voice messaging intervention delivered to mothers and fathers in Senegal on the consumption of a minimum acceptable diet and anemia prevalence in their children.

Who can participate

Age range

6 Months – 23 Months

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Exclusion criteria

Does not meet study inclusion criteria

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Number of Children Who Consume a Minimum Acceptable Diet

Timeframe: At study completion, an average of 4 months after baseline

Anemia Prevalence of Children

Timeframe: At study completion, an average of 4 months after baseline

Change in Percentage of Children Consuming a Minimum Acceptable Diet Between Baseline and Endline

Timeframe: Between baseline and study completion, an average of 4 months after baseline

Change in Percentage of Children With Anemia Between Baseline and Endline

Timeframe: Between baseline and study completion, an average of 4 months after baseline

Trial details

NCT IDNCT05374837

SponsorRutgers, The State University of New Jersey

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-15

Results submitted2024-05-21

View on ClinicalTrials.gov More Diet, Healthy trials

What they're measuring

Number of Children Who Consume a Minimum Acceptable Diet

Timeframe: At study completion, an average of 4 months after baseline

Anemia Prevalence of Children

Timeframe: At study completion, an average of 4 months after baseline

Change in Percentage of Children Consuming a Minimum Acceptable Diet Between Baseline and Endline

Timeframe: Between baseline and study completion, an average of 4 months after baseline

Change in Percentage of Children With Anemia Between Baseline and Endline

Timeframe: Between baseline and study completion, an average of 4 months after baseline