Optimizing Pregnancy and Treatment Interventions for Moms 2.0
Pregnancy, High Risk, Opioid-Related Disorders, Pregnancy Related
About this trial
This is an interventional health services research trial for Pregnancy, High Risk
Eligibility Criteria
Inclusion Criteria:
- Adult (≥18 years)
- English speaking
- Pregnant women (pregnancy status verified by gestational age >6 weeks from last menstrual period confirmed by ultrasound)
- OUD verified by examination of medical records for an OUD diagnosis, urine toxicology, and the Diagnostic and Statistical Manual of Mental Disorders (DSM) Checklist (modified from the DSM-IV to confirm current diagnosis for substance use disorders)
- Plan to carry their babies to delivery verified by patient self report
Participant Exclusion Criteria
- Experienced a psychotic or a manic episode in the last 30 days documented in their medical record
- Beyond the 25th week of gestation
- Cannot provide collateral contact information of 2 persons,
- Cannot provide a reliable phone number,
- Plan to move from the area within 2 months of their delivery will or 6 months after not be included in the study
- Inability or unwillingness of subject or legal guardian/representative to give written informed consent.
- Other factors that would cause harm or increased risk to the participant or close contacts, or preclude the participant's full adherence with or completion of the study
Sites / Locations
- Magee Women's Hospital
- University of Utah
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Control
Patient Navigation
The standard care condition includes brief case management and referral. The brief case management involves the participant speaking to a hospital social worker who conducts a patient needs assessment in the areas of behavioral health and social services. All patients will be referred to MAT and any identified behavioral health or social service needs.
The prenatal portion of the intervention includes 10 sessions delivered within approximately 14 weeks. The postnatal portion of the intervention will be delivered as 4 sessions over 8 weeks. Women who complete the intervention before delivery will receive regular calls/texts until delivery wherein the navigator will encourage and reinforce abstinence and treatment retention.