CompletedNot Applicable

The Effect of Maternal Dadiah Supplementation During Pregnancy on Child Growth and Gastrointestinal Health Outcomes

Indonesia52 participantsStarted 2020-08-20

Plain-language summary

The aim of our study is to assess the effect of giving dadiah as a supplement to pregnant women on improving the growth and digestive health of children.

Who can participate

Age range

20 Years – 35 Years

Sex

FEMALE

See this in plain English?

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

Inclusion Criteria: * Women with10-20 weeks gestation * Women give voluntary informed consent * Women willing to give exclusive breastfeeding * Women live in an area under study, registered, and visit antenatal care at targeted public health centers * Women plan to deliver babies in the area under study Exclusion Criteria: * Women having a medical history of HIV/AIDS, TBC, Hepatitis B. * Women with multiple pregnancies * Women having obesity, and/or another high-risk pregnancy (hypertension, preeclampsia, diabetes, bleeding history) * Received antibiotic treatment or intentionally consumes probiotic products during the preceding 4 weeks. (If the subject was on antibiotics before the beginning of the study or probiotics, a washout period of 2 weeks is required.)

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

Infant fecal gut microbiota proportion

Timeframe: three months

Breast milk gut microbiota proportion

Timeframe: three months

Level of infant fecal secretory Immunoglobulin A

Timeframe: three months

Level of breastmilk secretory Immunoglobulin A

Timeframe: three months

Trial details

NCT IDNCT05140928

SponsorAndalas University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-09-09

View on ClinicalTrials.gov More Gastrointestinal Microbiome trials

Who can participate

Age range

20 Years – 35 Years

Sex

FEMALE

See this in plain English?

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