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 @ 11:53 PM
Ignite Modification Date:
2025-12-24 @ 11:53 PM
NCT ID:
NCT02534051
Eligibility Criteria:
Inclusion Criteria:
* Inclusion criteria for clinics:
1. location in southwestern Ontario (for proximity to the research team),
2. availability of a clinician willing to serve as the local site lead, and
3. lack of any type of existing clinical care pathway for obese pregnant women
* Inclusion criteria for participants:
1. women with a pre-pregnancy (or in the event of inability to recall, then first measured) BMI \>30 kg/m2
2. with viable singleton pregnancies up to 20 weeks + 6 days gestational age upon first visit to randomized clinic
Exclusion Criteria:
* Women with:
1. a miscarriage or termination of pregnancy after enrollment,
2. twins or higher order multiples or
3. a fetus with a known lethal anomaly.
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT02534051
Study Brief:
Protocol Section:
NCT02534051