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 @ 12:28 AM
Ignite Modification Date:
2025-12-25 @ 12:28 AM
NCT ID:
NCT06996067
Eligibility Criteria:
INCLUSION CRITERIA:
Eligible birthing parents will (1) early postpartum (\<7 days) with their first child; (2) understand English; (3) have a cell phone with text and data; and (4) live in Nova Scotia. Eligible non-birthing parents will (1) be early postpartum (\<7 days) with their first child; (2) understand English; (3) have a cell phone with text and data; and (4) live in Nova Scotia.
EXCLUSION CRITERIA:
Participants (both birthing and non-birthing parents) will be excluded if: (1) newborn die or are expected to die prior to leaving the hospital; (2) they have no access to mobile phone, either personal or shared; (3) unwilling to receive SMS messages; (4) decline or withdraw to participate; or (5) participated in a previous iteration of this project (e.g., either the development or evaluation).
Healthy Volunteers:
True
Sex:
ALL
Study:
NCT06996067
Study Brief:
Protocol Section:
NCT06996067