Recruiting

INSPIRE

Sponsor:

University of Utah

Code:

NCT07707115

Conditions

Substance Use Disorders

Simulation Training

Pregnancy Related

Patient-centered Care

Bias, Implicit

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

INSPIRE

Study Details

Brief summary:

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.

Conditions

Substance Use Disorders

Simulation Training

Pregnancy Related

Patient-centered Care

Bias, Implicit

Study ID

NCT07707115

Start date

Aug 1, 2026

Status verified date

Aug, 2026

Completion date

Dec 31, 2027

Anticipated

Primary completion date

Dec 31, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Employed at the University of Utah Hospital
  • Directly interfaces with birthing individuals (as clinical or non-clinical team member, e.g., physician, nurse, emergency medical technician, social worker)
  • English speaking

Exclusion Criteria:

  • Unable to provide informed consent

Study Design

Enrollment

300 participants

Anticipated

Intervention Model

Sequential

Primary purpose

Health Services Research

Interventions and Outcome Measures

Arms

experimental: INSPIRE provider training

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.

Interventions

INSPIRE

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.

Primary outcome measure

  • Medical Condition Regard Scale (MCRS) [ Time Frame: Administered at Baseline and 1 month, 3 months, and 6 months after Baseline ]

Central Contacts and Locations

Central contacts

Assumpta Nantume

801-585-6011assumpta.nantume@hsc.utah.edu

Erin Johnson

801-646-7065erin.p.johnson@hsc.utah.edu

Locations

University of Utah Health

Recruiting

Salt Lake City, Utah, United States, 84102

Contacts

Assumpta Nantume

801-585-6011assumpta.nantume@hsc.utah.edu

More Information

Sponsor

University of Utah

Last update posted

Aug 10, 2026

Last verified

Aug, 2026

Keywords

  • substance use disorders
  • Care received in hospital during labor & delivery and post-partum

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by University of Utah on 2026-08-10.