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:
2025-12-25 @ 12:55 AM
Ignite Modification Date:
2025-12-25 @ 12:55 AM
NCT ID:
NCT02761967
Eligibility Criteria:
Inclusion Criteria:
* Do not suffer any absolute contraindications according to the American College of Obstetricians and Gynecologists.
* If there is a relative contraindication, participation in the intervention group should be favorable report by participants obstetrician.
* To know how to swim.
* To sign informed consent to participate in research consent.
Exclusion Criteria:
* Absolute contraindications to aerobic exercise during pregnancy.
* Restrictive lung disease.
* Heart disease with hemodynamic consequences.
* Incompetent cervix/cerclage.
* Multiple gestation with preterm labor.
* Persistent bleeding in the second or third trimester bleeding.
* Previa after 26 weeks of gestation.
* Preterm birth during the current pregnancy.
* Rupture of membranes.
* Pregnancy-induced hypertension.
* Relative contraindications to aerobic exercise during pregnancy.
* Severe anemia.
* Cardiac arrhythmia maternal unevaluated.
* Chronic Bronchitis.
* Type I diabetes poorly controlled.
* Extreme morbid obesity.
* Under extreme weight (BMI \<12).
* History of extremely sedentary life style.
* Intrauterine growth restriction in current pregnancy.
* Poorly controlled hypertension / pre-eclampsia.
* Orthopedic limitations.
* Poorly controlled seizure disorders.
* Poorly controlled Thyroid disease.
* Heavy smoker.
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT02761967
Study Brief:
Protocol Section:
NCT02761967