Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 6:49 PM
Ignite Modification Date:
2025-12-24 @ 6:49 PM
NCT ID:
NCT00088257
Eligibility Criteria:
Women were eligible for participation in Project Viva if they:
1. Were \<22 weeks pregnant
2. Planned to receive prenatal care at one of the selected clinics
3. Planned to deliver at one of the two study hospitals
4. Were able to answer questions in English
Women were ineligible if they:
1. Planned to terminate their pregnancy
2. Planned to move from the local area before the end of the follow-up period
3. Were pregnant with multiples (twins, triplets, etc)
Project Viva mother-child pairs were eligible for this study if they had provided maternal dietary date during pregnancy and a cord blood sample at delivery on which lymphocyte proliferation had been measured.
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT00088257
Study Brief:
Protocol Section:
NCT00088257