AzTrials
AzTrials

Substance Use Disorders (SUD)CEREMONYNCT06747442

Culturally Engaged REcovery: MOms Connected Through Native communitY

A study testing Cradleboard Journey in people with Substance Use Disorders (SUD) and Pregnancy, run by University of Utah at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

Pregnant and postpartum American Indian and Alaska Native people (Native mothers) face a more than two-fold higher risk of maternal mortality compared to non-Hispanic White mothers. Read more about this study

Who is it for?
Ages 18 years and older, women only
What is being tested?
Cradleboard Journey
Could I receive a placebo?
No, everyone receives an active treatment
How many people
270 participants
Where
1 siteUnited States
Study dates
26 May 2026to Mar 2029
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

CEREMONY Inclusion Criteria:

  • English or Spanish speaking
  • pregnant (verified by point of care urine pregnancy test)
  • plan to carry the fetus to delivery
  • identify as Indigenous, Native, Native American, American Indian or Alaska Native
  • willing to grant a release of information to allow study staff to contact other health care institutions and treatment centers and collect information from the medical record, e.g., date of delivery, infant admission etc.

CEREMONY Exclusion Criteria:

  • have a documented psychotic episode in the last 30 days
  • be >39 weeks of gestation
  • be unable provide collateral contact information of at least 1 person
  • be unable to provide reliable phone number
  • plan to move within 3 months of delivery

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Valerie Joseph Regulatory Coordinator contact

801-587-2249

valerie.joseph@hsc.utah.edu

United States1 site, 1 recruiting
  • Sacred Circle Healthcare

    Salt Lake City, Utah, 84111

    Recruiting

Other trials in United States

About this study

Official title: Culturally Engaged REcovery - MOms Connected Through Native communitY (CEREMONY)

Pregnant and postpartum American Indian and Alaska Native people (Native mothers) face a more than two-fold higher risk of maternal mortality compared to non-Hispanic White mothers. Deaths related to substance use (SU) and mental health conditions are a leading cause of preventable maternal mortality, including among Native mothers, making these conditions a strong target for reducing maternal mortality and morbidity. The objective of this study is to 1) adapt evidence-based perinatal care models that integrate pregnancy and postpartum care with SU treatment and care to meet the needs of Native mothers, and 2) assess the implementation and efficacy of that model for participants with substance use disorder who identify as Native receiving prenatal care at Sacred Circle Healthcare in Salt Lake City, Utah.

Read the detailed description

Pregnant and postpartum American Indian and Alaska Native people (Native mothers) face a more than two-fold higher risk of maternal mortality compared to non-Hispanic White mothers. Deaths related to substance use (SU) and mental health conditions reflect a leading cause of preventable maternal mortality, including among Native mothers, making these conditions a strong target for reducing maternal mortality and morbidity. The Utah Maternal Mortality Review Committee (MMRC) has identified access to substance use disorder (SUD) treatment including medication for opioid use disorder (MOUD), mental health care, improved social support, decreased stigma against SUD, and care coordination, particularly in the postpartum period (when the majority of deaths occur) as actionable intervention points. The objective of this study, Culturally-Engaged REcovery - MOms connected through Native CommunitY (CEREMONY), is to adapt evidence-based perinatal care models that integrate pregnancy and postpartum care with SU/SUD treatment and care to meet the needs of Native mothers. With a partnership at Sacred Circle Clinic, a federal Tribal Contract clinic operated by the Confederated Tribes of the Goshute Reservation, the investigators are uniquely poised to respond to the expressed needs of Native mothers and stakeholders, who identified a lack of culturally-integrated SUD care as a significant gap in perinatal care for Native mothers. The investigators will do this by building upon the strong, evidence-based foundation of the University of Utah integrated perinatal SUD clinic called Substance Use and Pregnancy - Recovery, Addiction, and Dependence (SUPeRAD). The SUPeRAD model directly addresses the actionable intervention points identified by the MMRC to prevent SUD-related maternal deaths, but is not specifically adapted to Native mothers' needs. The rationale for this study is that there is a critical knowledge gap in the adaptation and implementation of integrated perinatal SUD care specifically for Native mothers. The CEREMONY study will fill this gap by adapting the SUPeRAD clinic model to the needs of Native mothers using the validated ADAPT-ITT adaptation framework, informed by human centered design and community-based participatory research (Aim 1; not part of the observation trial submission described on this website); and then studying the adapted, culturally-integrated perinatal SUD care intervention at Sacred Circle Healthcare using a Hybrid Type 1 effectiveness-implementation study (Aim 2a\&b). The Hybrid Type 1 design will provide important, reliable data on the clinical effectiveness of culturally adapted perinatal SUD care for Native mothers (Aim 2a) while also producing novel data on the implementation process (Aim 2b). Successful completion of these Aims will provide implementation and training protocols that can be used to guide adaptation and implementation of culturally-adapted perinatal SUD care in other settings across the US.

Sacred Circle Healthcare will be implementing the new care model and offering it to all patients who identify as Native and having a substance use disorder. Within that group, the CEREMONY study will invite patients who meet study inclusion criteria to participate in the observational research study.

Participants enrolled prospectively will be compared to a historical cohort, with data pulled from the Utah Population Database, for our primary outcome. The historical cohort will be comprised on deidentified data from individuals over 18 years old with delivery of an infant greater than 20 weeks' gestation between 2020 and the most recent year of available data (approximately 2027-28) who had at least one visit with a Utah health provider before delivery and identify as American Indian/Alaska Native based on vital records or hospital records.

Being tested
Cradleboard Journey
Keywords
Pregnancy, Prenatal care, Substance Use Disorder, Native and Indigenous Health, Culturally adapted care
Medical subject headings
Substance-Related Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Cradleboard JourneyBehavioural

    Cradleboard Journey is an integrated perinatal substance use disorder group clinical program specifically created for Native mothers.

Study groups in NCT06747442
Study groupRoleWhat they receive
CEREMONYExperimentalAny Native individuals seeking treatment in the integrated perinatal SUD clinical program specifically created for Native mothers may opt to enroll in prospective data collection during their time in the program
Receives: Behavioral: Cradleboard Journey
Contemporary comparison cohortNo interventionUtah Population Database will be queried for individuals who could have met criteria for prospective data collection but did not participate in the SUD clinical program. The outcomes of these individuals (administrative data only) will be compared to individuals taking part in the SUD program for Native pregnant people who agree to have their data collected.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Postpartum engagement in care

    Completion of a postpartum follow up visit within 8 weeks of delivery

    Measured: From enrollment until 12 weeks after delivery

Secondary outcomes (1)
  1. Medication for opioid use disorder

    Any prescription of suboxone or methadone for individuals with OUD, and the length of time the prescription is kept current

    Measured: Enrollment through 1 year postpartum

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Dec 2024
  2. Study start26 May 2026
  3. Primary completionDec 2028 (estimated)
  4. Study completionMar 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Non-randomised
Intervention model
Single group
Model description
We will complete a type I hybrid effectiveness-implementation study to provide important data on clinical effectiveness by comparison to a historical cohort, with a robust statistical analysis plan to address selection bias. We plan to recruit 150 participants prospectively, with an expected final enrollment of 120, and compare them to a deidentified historical cohort of roughly 120 individuals.
Masking
None (open label)
Enrolment
270 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06747442
Sponsor's protocol ID
00177269
Other IDs
U54HD113169
Acronym
CEREMONY
Status last verified
Jul 2026
First submitted
18 Dec 2024
Last updated
7 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Data sovereignty is of critical importance when working with Native communities. Particularly with recent data breaches in Utah related to Native individuals' health data, a clear and strictly adhered-to data management policy is critical. The memorandum of understanding between the University of Utah and Sacred Circle includes a data sovereignty plan, which includes a statement that data is owned by the Tribal entity. Data will be deidentified before sharing on a need to know basis, on the agreement that once the data analysis is complete, the data will be returned to the Tribal entity or destroyed.

Publications

  • Debbink MP, Tanana H, Murray JL, Blosser P, Horse L, Monroy C, Spiess S, Charles JE, Turok DK, Smid MC, Allshouse AA, Smith JD, Cohen SR, Johnson EP, Metz TD, Gordon AJ. Culturally Engaged REcovery - MOms connected through Native CommunitY (CEREMONY): An Implementation Study to Evaluate the Adaptation and Implementation of an Integrated Perinatal SUD Clinical Model for Pregnant and Postpartum Native People. Subst Use Addctn J. 2026 Jan;47(1):233-242. doi: 10.1177/29767342251336550. Epub 2025 Sep 15.

    PubMed 40955087

Questions about this trial

What is this clinical trial studying?

A study testing Cradleboard Journey in people with Substance Use Disorders (SUD) and Pregnancy, run by University of Utah at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 7 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Valerie Joseph Regulatory Coordinator (801-587-2249, valerie.joseph@hsc.utah.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Postpartum engagement in care (time frame: From enrollment until 12 weeks after delivery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06747442, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Jul 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in