Enrolling by invitation

BELIEVEInterprofessional Education in Virtual Reality for Maternal Healthcare

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Study Aim

This study aims to assess the impact of virtual reality-based interprofessional education on reducing severe postpartum pain in new mothers.

What is being tested

BELIEVE IPE Training

+ Usual Care

BehavioralOther
Who is being recruted

Neurologic Manifestations+1

+ Pain

+ Signs and Symptoms

From 18 to 99 Years
See all eligibility criteria
How is the trial designed

Supportive Care Study

Placebo-Controlled
Interventional
Study Start: July 2024
See protocol details

Summary

Principal SponsorUniversity of North Carolina, Chapel Hill
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: July 1, 2024

Actual date on which the first participant was enrolled.

This study aims to create a new educational program that uses virtual reality to train healthcare professionals. The focus is on improving the experiences of patients who are receiving maternal healthcare, which includes care during pregnancy, childbirth, and postpartum. The program is designed to reduce disparities, meaning it seeks to provide equal care for all patients regardless of their background or circumstances. By educating healthcare teams together in this innovative way, the study hopes to ensure that everyone gets the best possible care during such a crucial time. Participants in the study will engage with a curriculum that is delivered through virtual reality, offering an immersive learning experience. The study uses a step-wedge design, meaning that different groups will start the program at different times. This approach helps in evaluating the program's effectiveness over time. While the study does not include specific outcomes like medical tests or procedures, it focuses on how this educational approach might improve the quality of maternal healthcare services. The potential benefit is a more equitable and positive healthcare experience for mothers, which is vital for their well-being and that of their babies.

Official TitleBuilding Equitable Linkages With Interprofessional Education Valuing Everyone
Principal SponsorUniversity of North Carolina, Chapel Hill
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

32000 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 99 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Neurologic ManifestationsPainSigns and SymptomsPathological Conditions, Signs and Symptoms

Criteria

Inclusion Criteria: Healthcare Team Participants * Employed as one of the following roles: maternity care provider, nurse, lactation consultant or doula. * Primary inpatient clinical assignment is maternity care. * If Per Diem: Employed for a minimum of 4 shifts/month at a participating site. Birthing Parent Data Extraction Participants • Had a live birth at a participating site from the start of the study through the last Data Retrieval timepoint. Birthing Parent Interview Participants * Had a live birth at a participating site from the start of the study through the last Data Retrieval timepoint. * Black race or Limited English Proficiency with preferred language of Spanish. * Age ≥ 18. Exclusion Criteria: Healthcare Team Participants • None Birthing Parent Data Extraction Participants • Baby with birth gestational age \< 24 weeks. Birthing Parent Interview Participants * Baby with birth gestational age \< 24 weeks. * Baby is no longer alive at time of Data Retrieval (regardless of gestational age). * Currently incarcerated. * Previously completed a birthing parent interview for the BELIEVE study. * Previously enrolled as a Healthcare Team Participant.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Active Comparator
In the post-intervention sequence(s), birthing people at participating hospitals will experience treatment by health care teams that have undergone the Building Equitable Linkages With Interprofessional Education Valuing Everyone interprofessional education (BELIEVE IPE) training.

Group II

Placebo
In the pre-intervention sequence(s), birthing people at participating hospitals will experience treatment-as-usual.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

University of North Carolina

Chapel Hill, United StatesOpen University of North Carolina in Google Maps
Enrolling by invitationOne Study Center