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 @ 10:02 PM
Ignite Modification Date:
2025-12-24 @ 10:02 PM
NCT ID:
NCT02791932
Eligibility Criteria:
Inclusion Criteria:
* less than 20 weeks pregnant
* must speak English or Spanish
* willing to be randomly assigned to either of the two study arms
* healthcare provider consent
* access to a telephone (92% of low income women have access to a telephone and Minnesota offers free phone access for low income individuals; Fasts, 2015)
* being at risk for depression (defined as having a history of depression) but are not currently depressed.
* consistent with prior research, history of depression will be defined as ever being told by a healthcare provider that she has depression and/or being prescribed an antidepressant for depression.
Exclusion Criteria:
* less than 18 years of age
* currently exercising 60 or more minutes per week
* unable to exercise for 20 minutes continuously
* history of heart disease, lung disease, anemia, musculoskeletal problems (e.g., arthritis, gout, osteoporosis, or back, hip or knee pain that may interfere with exercising), poorly controlled hypertension, seizure disorder, exercise induced asthma, or any other medical condition that would make exercise unsafe
* taking medication that interferes with heart rate responses to exercise such as beta blockers; participating in another exercise or weight management study
* another member of the household participating in the study
* currently receiving antidepressant medication or psychotherapy for depression; - hospitalization for a psychiatric disorder during previous six months
* pregnant with multiple fetuses.
* participants depressed at the baseline assessment will be referred to their healthcare provider.
* there will have a safety protocol in place for worsening symptoms of depression and suicidal ideation
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT02791932
Study Brief:
Protocol Section:
NCT02791932