Improving Maternal and Child Health Through Prenatal Fatty Acid Supplementation (NCT02647723) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Improving Maternal and Child Health Through Prenatal Fatty Acid Supplementation
United States168 participantsStarted 2016-01
Plain-language summary
The purpose of the study is to test whether nutritional supplementation during pregnancy is associated with 1) improved maternal health during pregnancy; 2) improved infant birth and neurodevelopmental outcomes, and 3) whether the association between nutritional supplementation during pregnancy and infant outcomes is partially mediated by reductions in maternal perceived stress and stress reactivity during pregnancy.
Who can participate
Age range
18 Years – 34 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:
* Age between 18 and 34
* Household recipient of public assistance (e.g. Medicaid insurance) due to low income
* Low levels of DHA consumption as defined as less than two fish servings per week
Exclusion Criteria:
* Reports of known medial complications
* Regular use of steroid medications, alcohol, cigarettes, or illegal substances (by maternal report)
* Use of blood thinners or anti-coagulants
* Use of psychotropic medications
* Allergy to iodine and/or soy
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
1
Average Change in Perceived Stress Scale (PSS) Score From Visit 1 to Visit 4
Timeframe: 16 months
2
Average Change in Perceived Stress Scale (PSS) Score From Visit 1 to Visit 3