← Back to Clinical Trials
Recruiting NCT06790641

NCT06790641 Pathways to Perinatal Mental Health Equity

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06790641
Status Recruiting
Phase
Sponsor University of Massachusetts, Worcester
Condition Perinatal Anxiety
Study Type INTERVENTIONAL
Enrollment 1,270 participants
Start Date 2025-12-05
Primary Completion 2030-10-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 70 Years
Study Type INTERVENTIONAL
Interventions
Program in Support of Moms (PRISM)PSI Peer Support

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 1,270 participants in total. It began in 2025-12-05 with a primary completion date of 2030-10-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Mental health conditions occurring during pregnancy and up to one year postpartum (the perinatal period) occur in 1 in 5 perinatal individuals. To improve mental health care during the perinatal period, this study will implement and compare a health care model of improving mood and anxiety disorder care in practices with a health care-community partnership model. The study will include 32 perinatal care settings across the United States. Half of them will have the health care model, the other half will have the health care-community partnership model. The study is designed to answer the question, "Should states and healthcare systems put resources into a healthcare system approach or a healthcare-community partnership approach to mental health care?" The results of this study will help states and healthcare systems decide how to develop pathways for increasing access to mental health care for pregnant and postpartum individuals.

Eligibility Criteria

Inclusion Criteria for perinatal care setting team members: * Be employed by a participating perinatal care setting in a clinical role (including as an obstetrician-gynecologist, midwife, nurse practitioner, a nurse, a navigator, or administrative staff member who implemented the respective intervention during the study period). * Be 18 years of age or older * Provide verbal consent prior to the focus group or interview * Be proficient in English Inclusion Criteria for peer mentors: * Have completed PSI training to be a peer mentor * Be 18 years of age or older * Provide verbal consent prior to the focus group or interview * Be proficient in English Inclusion Criteria for perinatal individuals: * Have received perinatal care at a study partnering perinatal care setting during the study period * Be 18 years of age or older * Provide verbal consent prior to the focus group or interview * Be proficient in English or Spanish Exclusion Criteria: An individual who does not meet the inclusion criteria listed above will be excluded from participation in this study. There are no additional exclusion criteria.

Contact & Investigator

Central Contact

Rebekah Getman, PhD

✉ Rebekah.Getman2@umassmed.edu

📞 6177636460

Principal Investigator

Nancy Byatt, DO, MS, MBA

PRINCIPAL INVESTIGATOR

UMass Chan Medical School and UMass Memorial Health

Frequently Asked Questions

Who can join the NCT06790641 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 70 Years, studying Perinatal Anxiety. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06790641 currently recruiting?

Yes, NCT06790641 is actively recruiting participants. Contact the research team at Rebekah.Getman2@umassmed.edu for enrollment information.

Where is the NCT06790641 trial being conducted?

This trial is being conducted at Shrewsbury, United States.

Who is sponsoring the NCT06790641 clinical trial?

NCT06790641 is sponsored by University of Massachusetts, Worcester. The principal investigator is Nancy Byatt, DO, MS, MBA at UMass Chan Medical School and UMass Memorial Health. The trial plans to enroll 1,270 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology