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| ID | Type | Description | Link |
|---|---|---|---|
| U54HD113169 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) | NIH |
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The goal of this clinical trial is to develop and evaluate INSPIRE, an intervention for healthcare teams to improve care for individuals with substance use disorder (SUD) during their peri-delivery care. The main question it aims to answer is whether healthcare provider stigmas and behaviors change after receiving the training. The study will be implemented at the University of Utah.
Individuals with substance use disorder (SUD) face a higher risk of severe maternal morbidity and mortality. Provider stigma contribute to these outcomes by attenuating the provision of evidence-based, person-centered care. The goal of this study is to evaluate INSPIRE, an intervention for interprofessional healthcare teams to improve care for individuals with substance use disorder (SUD) during their peri-delivery care. INSPIRE includes three core modules (an online training on SUD in birth, an in-person simulation training, and an additional online training to assess and build clinical empathy skills). We will evaluate INSPIRE at the University of Utah hospital using a quasi-experimental design to determine impact on healthcare team outcomes. We will enroll up to 300 healthcare team members across clinical specialties that support birthing individuals. All enrolled providers will receive INSPIRE training, and assessments will be conducted at baseline, 1 month, 3 months, and 6 months. The primary outcome for providers is stigma. We will assess change in stigma scores from baseline to 6 months using a mixed effects linear regression model, specified to provide a paired-sample comparison between pre- and post-intervention scores.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| INSPIRE provider training | Experimental | All providers will receive the INSPIRE intervention. The INSPIRE intervention includes: 1) online learning modules #1, which is completed individually and should take approximately 2 hours, and 2) in-person simulation, which is done as a group and scheduled for 4 hours, and 3) online learning module #2. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| INSPIRE | Behavioral | The INSPIRE intervention includes: 1) online learning modules #1, which is completed individually and should take approximately 2 hours, and 2) in-person simulation, which is done as a group and scheduled for 4 hours, and 3) online learning module #2. |
| Measure | Description | Time Frame |
|---|---|---|
| Medical Condition Regard Scale (MCRS) | MCRS is | Administered at Baseline and 1 month, 3 months, and 6 months after Baseline |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Assumpta Nantume | Contact | 801-585-6011 | assumpta.nantume@hsc.utah.edu | |
| Erin Johnson | Contact | 801-646-7065 | erin.p.johnson@hsc.utah.edu |
| Name | Affiliation | Role |
|---|---|---|
| Susanna Cohen, DNP, CNM, CHSE, FAAN | University of Utah | Principal Investigator |
| Melissa Watt, PhD | University of Utah | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Utah Health | Salt Lake City | Utah | 84102 | United States |
Deidentified data aligning with the Maternal Health Common Data Elements outlined by the IMPROVE Data Hub will be shared with the Maternal Health Data Innovation and Coordination Hub ("Data Hub"). The Data Hub will determine timing and methods of sharing gathered data from IMPROVE Centers and uploading congregated data into DASH.
Supporting information will be shared with the Data Hub within 6 months of the completion of data collection, and available through DASH for as long as DASH maintains the data.
All deidentified data and supporting information will be maintained by the DASH. Access will be determined by the structures set forth by the Data Hub and DASH.
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| ID | Term |
|---|---|
| D019966 | Substance-Related Disorders |
| D000087302 | Bias, Implicit |
| ID | Term |
|---|---|
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
| D011287 | Prejudice |
| D012919 | Social Behavior |
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Providers will be assessed at baseline prior to intervention exposure, at midline (between modules 2 and 3, roughly 2 months later) and at post (6 months after baseline)
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| D001519 |
| Behavior |