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| ID | Type | Description | Link |
|---|---|---|---|
| 1R01DA049759-01 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute on Drug Abuse (NIDA) | NIH |
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This research will test the effectiveness of a prenatal provider education and training program designed to facilitate provider adoption of evidence-based practices for the treatment of OUD during pregnancy. Findings from this research will provide high quality evidence about how to increase evidence-based treatment for pregnant women with OUD and subsequent maternal-child health outcomes.
The prevalence of opioid use disorder (OUD) during pregnancy has quadrupled over the past decade, as have maternal and neonatal morbidity and mortality related to substance use. Medication assisted treatment (MAT) use during pregnancy reduces adverse outcomes and is the recommended, evidence-based practice (EBP) for OUD treatment during pregnancy. Despite this, 40% of pregnant women with OUD do not receive MAT. Currently, there are no effective strategies to expand MAT access and availability for pregnant women, especially in rural, low-resource settings where maternal opioid use is disproportionately high. As an initial step to address this gap, the investigators engaged key stakeholders across a large health system in Pennsylvania to determine barriers and facilitators to expanding treatment services in high need, low-resource obstetric settings. The stakeholders identified a critical need for a women-centered, low resource, sustainable, provider-level intervention to facilitate the adoption of MAT in obstetric settings. Therefore, the investigators objective is to test the effectiveness of a prenatal provider education and training program designed to facilitate the adoption of EBP for OUD during pregnancy called Project STEPuP (Substance abuse Treatment and Education during pregnancy and Postpartum). Project STEPuP, grounded in preliminary and pilot work conducted by the research team, has 4 components designed to address barriers to MAT and EBP adoption: 1) a "hub and spoke," remotely supported provider education and training program, 2) addiction teleconsultation support, 3) case management and telepsychiatry support, and 4) a partnership with health system administrators and payers to address administrative and reimbursement related needs. To achieve this objective, the research team will conduct a cluster-randomized clinical trial across 12 obstetric sites in Pennsylvania and New York. Outcomes among 870 patients will be assessed during pregnancy, at delivery and through 1 year postpartum. The investigators central hypothesis is that Project STEPuP will facilitate EBP adoption, increase MAT utilization and improve health outcomes among pregnant and postpartum women with OUD and their children. Specifically, the investigators aim to: 1) Create organizational readiness to facilitate Project STEPuP implementation; 2) Assess the effect of Project STEPuP on provider adoption of EBP for OUD during pregnancy; and 3) Evaluate the effect of provider adoption of EBP on maternal and child health outcomes. The investigators research is significant by addressing the substantial knowledge gap of how to increase MAT use in pregnancy and innovative by examining the role that prenatal providers can play in expanding treatment access.
Study outcome measures refined in January 2024 to align with grant proposal and increase readability.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| STEPuP Intervention | Experimental | STEPuP interventions |
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| Usual Care | Active Comparator | Standard of Care |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| STEPuP Intervention | Behavioral | Project STEPup has 4 components designed to address barriers to MAT and EBP adoption: 1) a "hub and spoke" remotely-supported provider education and training program, 2) addiction teleconsultation support, 3) case management and telepsychiatry support, and 4) a partnership with health system administrators and payers to address administrative and reimbursement related needs. |
| Measure | Description | Time Frame |
|---|---|---|
| Patient Medication-assisted treatment (MAT) utilization | As measured by total count of weeks in pregnancy with any Medications for Opioid Use Disorder (MOUD) either buprenorphine or methadone, use during pregnancy | up to 1 year post delivery |
| Provider Provision of Buprenorphine | As measured by total number of patients within a prenatal practice with opioid use disorder that receive MOUD treatment (either buprenorphine or methadone) | up to 1 year post delivery |
| Measure | Description | Time Frame |
|---|---|---|
| Hepatitis C Virus (HCV) Screening Rate | Number of participants screened for Hepatitis C Virus (HCV) as measured by related laboratory testing | during pregnancy (up to 40 weeks) |
| Human Immunodeficiency Virus (HIV) Screening Rate |
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Inclusion Criteria:
Providers:
Patient:
Maternal and child outcome data will be collected from the Electronic Health Record (EHR) and individual patients will not be recruited to participate in the randomized controlled trial (RCT).
Inclusion criteria for a small subset of pregnant women will be recruited for a one-time qualitative interview (n=50):
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Elizabeth Krans, MD | UPMC Magee-Womens Hospital | Principal Investigator |
| Marian Jarlenski, PhD | University of Pittsburgh | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Magee Womens Hospital of UPMC | Pittsburgh | Pennsylvania | 15213 | United States |
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| ID | Term |
|---|---|
| D009293 | Opioid-Related Disorders |
| ID | Term |
|---|---|
| D000079524 | Narcotic-Related Disorders |
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
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| ID | Term |
|---|---|
| D049590 | Postpartum Period |
| ID | Term |
|---|---|
| D055703 | Reproductive Physiological Phenomena |
| D012101 | Reproductive and Urinary Physiological Phenomena |
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| Usual Care | Behavioral | Standard of Care |
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Number of participants screened for Human Immunodeficiency Virus (HIV) as measured by related laboratory testing
| during pregnancy (up to 40 weeks) |
| Mental Health Screening Rate | Number of participants who received a mental health screening test, Patient Health Questionaire-2 or Patient Health Questionaire-9 (PHQ-2 or PHQ-9) | during pregnancy (up to 40 weeks) |
| Contraceptive Utilization Rate | Number of participants utilizing postpartum contraceptive as measured by contraception prescription | delivery up to 1 year post delivery |
| Breastfeeding Rate | Number of participants breastfeeding as measured by feeding records from infant charts (yes/no) | delivery up to 1 year post delivery |