search
Back to results

Optimizing Pregnancy and Treatment Interventions for Moms 2.0

Primary Purpose

Pregnancy, High Risk, Opioid-Related Disorders, Pregnancy Related

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Patient Navigation
Sponsored by
University of Utah
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Pregnancy, High Risk

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult (≥18 years)
  • English speaking
  • Pregnant women (pregnancy status verified by gestational age >6 weeks from last menstrual period confirmed by ultrasound)
  • OUD verified by examination of medical records for an OUD diagnosis, urine toxicology, and the Diagnostic and Statistical Manual of Mental Disorders (DSM) Checklist (modified from the DSM-IV to confirm current diagnosis for substance use disorders)
  • Plan to carry their babies to delivery verified by patient self report

Participant Exclusion Criteria

  • Experienced a psychotic or a manic episode in the last 30 days documented in their medical record
  • Beyond the 25th week of gestation
  • Cannot provide collateral contact information of 2 persons,
  • Cannot provide a reliable phone number,
  • Plan to move from the area within 2 months of their delivery will or 6 months after not be included in the study
  • Inability or unwillingness of subject or legal guardian/representative to give written informed consent.
  • Other factors that would cause harm or increased risk to the participant or close contacts, or preclude the participant's full adherence with or completion of the study

Sites / Locations

  • Magee Women's Hospital
  • University of Utah

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Patient Navigation

Arm Description

The standard care condition includes brief case management and referral. The brief case management involves the participant speaking to a hospital social worker who conducts a patient needs assessment in the areas of behavioral health and social services. All patients will be referred to MAT and any identified behavioral health or social service needs.

The prenatal portion of the intervention includes 10 sessions delivered within approximately 14 weeks. The postnatal portion of the intervention will be delivered as 4 sessions over 8 weeks. Women who complete the intervention before delivery will receive regular calls/texts until delivery wherein the navigator will encourage and reinforce abstinence and treatment retention.

Outcomes

Primary Outcome Measures

Opioid Use Disorder (OUD) and other Substance Use Disorder (SUD) Treatment Linkage/Retention
OUD and other SUD treatment linkage/retention will be assessed through the treatment services review (TSR-6). The TSR-6 is a clinically validated 56-item measure with excellent reliability. We will capture frequency of meetings, sessions, day in OUD and other substance counseling.
Opioid Abstinence
Opioid abstinence will be accessed using a 14-panel urine toxicology screening.
Adherence to Medication-Assisted Treatment (MAT)
Adherence to MAT will be accessed using a 14-panel urine toxicology screening.
Adherence to Medication-Assisted Treatment (MAT)
Adherence to MAT will be assessed through the treatment services review (TSR-6) medication use section.
Linkage/Retention in Psychosocial Services
Linkage/retention in psychosocial services will be accessed through medical record review.

Secondary Outcome Measures

Adequacy of Prenatal Care
Capturing prenatal care will be accessed through the adequacy of prenatal care utilization index (APNCU). This index will be used to determine the sufficiency of prenatal care participants received.
Needle use and safe sex frequency
The Risk Behavior Survey (RBA) will be used to access HIV/Hepatitis C virus (HCV) risk behaviors. The RBA is a self-report, 22-item assessment provides the highest 30-day reliability among standardized instruments for HIV/HCV-risk behaviors among drug users.
Incidence of depression and anxiety
The patient health questionnaire (PHQ) will be used to assess mental health. The PHQ is an 11-item mental health assessment with demonstrated criterion validity and reliability. The PHQ accesses depression, suicide ideation, anxiety, somatoform, eating and alcohol use disorders.
Child and mother bond following delivery
Child and mother indicators will be accessed through the Maternal-Fetal Attachment survey.

Full Information

First Posted
January 28, 2019
Last Updated
November 7, 2022
Sponsor
University of Utah
Collaborators
University of Pittsburgh
search

1. Study Identification

Unique Protocol Identification Number
NCT03833245
Brief Title
Optimizing Pregnancy and Treatment Interventions for Moms 2.0
Official Title
Optimizing Pregnancy and Treatment Interventions for Moms 2.0
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
March 11, 2019 (Actual)
Primary Completion Date
October 1, 2022 (Actual)
Study Completion Date
October 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Utah
Collaborators
University of Pittsburgh

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The US opioid epidemic continues to result in serious health consequences for pregnant and postpartum women. In the US from 2007 to 2012, an average of 21,000 pregnant women each year reported past month opioid misuse. This study aims to provide rapid and targeted primary prevention activities aimed at assisting pregnant women with opioid use disorder (OUD) to become linked to and retained in treatment in order to reduce harms to them (including overdose) and their offspring.
Detailed Description
Age adjusted rates for overdose among women in the US increased more than six-fold from 1.4 in 1999 to 8.5 in 2016. Examining Pennsylvania (PA) and Utah (UT; the states where recruitment will happen in this study), these states have some of the highest rates of overdose among women compared to other US states. Specifically, PA's overdose rate among women surpassed the national average in 2016, and rates of overdose death in UT among women have ranged 2-9 times higher than the national rate between 2009 to 2016. Both PA and Utah are among the states with the highest opioid prescribing to pregnant women, with Utah being the highest in the nation (41.6%). Prenatal opioid use disorder (OUD) in the US has brought serious health consequences for mother and infant-including preterm delivery, low birth weight, NAS, and poor breastfeeding, and includes substantial expenditures of health care resources. Chances for HIV (OR=20.3, 95% CI = 13.8-29.7) and hepatitis C virus (OR=150.2. 95% CI = 120.9-186.6) infection among women with OUD are markedly higher than for those without OUD. Pregnant women with OUD have high rates of psychiatric illnesses, such as depression and anxiety, and other substance use disorders (SUDs), with particularly high rates of smoking (>80%). Neonatal abstinence syndrome (NAS), an opioid withdrawal syndrome among neonates, has also increased substantially from 3.4/1000 births in 2009 to 5.8/1000 births in 2012. Poly-substance use among pregnant women with OUD has also been associated with higher levels of needed medications to treat NAS and longer duration of NAS treatment. Smoking combined with opioid use during pregnancy has likewise been related to longer duration of NAS treatment, greater NAS severity, and higher levels of medication needed to treat NAS symptomology. Any prenatal opioid use also has been associated with birth defects, including neural tube defects, conoventricular septal defects, atrioventricular septal defects, hypoplastic left heart syndrome, and gastroschisis. Compared with women without any SUDs, children born to mothers with OUD or OUD plus other SUDs also have been documented to have lower cognitive functioning as they mature. Problems resulting from illicit and prescription OUD also result in significant social issues. Pregnant women with OUD have been observed to have financial and housing instability, challenges related to employment, and involvement with the legal system.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy, High Risk, Opioid-Related Disorders, Pregnancy Related

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
106 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
The standard care condition includes brief case management and referral. The brief case management involves the participant speaking to a hospital social worker who conducts a patient needs assessment in the areas of behavioral health and social services. All patients will be referred to MAT and any identified behavioral health or social service needs.
Arm Title
Patient Navigation
Arm Type
Experimental
Arm Description
The prenatal portion of the intervention includes 10 sessions delivered within approximately 14 weeks. The postnatal portion of the intervention will be delivered as 4 sessions over 8 weeks. Women who complete the intervention before delivery will receive regular calls/texts until delivery wherein the navigator will encourage and reinforce abstinence and treatment retention.
Intervention Type
Behavioral
Intervention Name(s)
Patient Navigation
Intervention Description
The patient navigation (PN) intervention will initiate following participant recruitment. It is important to note that PN sessions do not strictly coincide with specific weeks of pregnancy since the women can be recruited up to ≤25 weeks of gestation. The prenatal portion of the intervention includes 10 sessions delivered within approximately 14 weeks. The postnatal portion of the intervention will be delivered as 4 sessions over 8 weeks. Women who complete the intervention before delivery will receive regular calls/texts until delivery wherein the navigator will encourage and reinforce abstinence and treatment retention. All contact will be reported by staff in a patient contact log developed for the study that will be used to quantify level of patient contact.
Primary Outcome Measure Information:
Title
Opioid Use Disorder (OUD) and other Substance Use Disorder (SUD) Treatment Linkage/Retention
Description
OUD and other SUD treatment linkage/retention will be assessed through the treatment services review (TSR-6). The TSR-6 is a clinically validated 56-item measure with excellent reliability. We will capture frequency of meetings, sessions, day in OUD and other substance counseling.
Time Frame
36 months
Title
Opioid Abstinence
Description
Opioid abstinence will be accessed using a 14-panel urine toxicology screening.
Time Frame
36 months
Title
Adherence to Medication-Assisted Treatment (MAT)
Description
Adherence to MAT will be accessed using a 14-panel urine toxicology screening.
Time Frame
36 months
Title
Adherence to Medication-Assisted Treatment (MAT)
Description
Adherence to MAT will be assessed through the treatment services review (TSR-6) medication use section.
Time Frame
36 months
Title
Linkage/Retention in Psychosocial Services
Description
Linkage/retention in psychosocial services will be accessed through medical record review.
Time Frame
36 months
Secondary Outcome Measure Information:
Title
Adequacy of Prenatal Care
Description
Capturing prenatal care will be accessed through the adequacy of prenatal care utilization index (APNCU). This index will be used to determine the sufficiency of prenatal care participants received.
Time Frame
36 months
Title
Needle use and safe sex frequency
Description
The Risk Behavior Survey (RBA) will be used to access HIV/Hepatitis C virus (HCV) risk behaviors. The RBA is a self-report, 22-item assessment provides the highest 30-day reliability among standardized instruments for HIV/HCV-risk behaviors among drug users.
Time Frame
36 months
Title
Incidence of depression and anxiety
Description
The patient health questionnaire (PHQ) will be used to assess mental health. The PHQ is an 11-item mental health assessment with demonstrated criterion validity and reliability. The PHQ accesses depression, suicide ideation, anxiety, somatoform, eating and alcohol use disorders.
Time Frame
36 months
Title
Child and mother bond following delivery
Description
Child and mother indicators will be accessed through the Maternal-Fetal Attachment survey.
Time Frame
36 months

10. Eligibility

Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult (≥18 years) English speaking Pregnant women (pregnancy status verified by gestational age >6 weeks from last menstrual period confirmed by ultrasound) OUD verified by examination of medical records for an OUD diagnosis, urine toxicology, and the Diagnostic and Statistical Manual of Mental Disorders (DSM) Checklist (modified from the DSM-IV to confirm current diagnosis for substance use disorders) Plan to carry their babies to delivery verified by patient self report Participant Exclusion Criteria Experienced a psychotic or a manic episode in the last 30 days documented in their medical record Beyond the 25th week of gestation Cannot provide collateral contact information of 2 persons, Cannot provide a reliable phone number, Plan to move from the area within 2 months of their delivery will or 6 months after not be included in the study Inability or unwillingness of subject or legal guardian/representative to give written informed consent. Other factors that would cause harm or increased risk to the participant or close contacts, or preclude the participant's full adherence with or completion of the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerald Cochran, PhD
Organizational Affiliation
University of Utah
Official's Role
Principal Investigator
Facility Information:
Facility Name
Magee Women's Hospital
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Facility Name
University of Utah
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84108
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35349380
Citation
Bryan MA, Mallik D, Cochran G, Lundahl B. Mindfulness and Savoring: A Commentary on Savoring Strategies and Their Implications for Addiction Treatment. Subst Use Misuse. 2022;57(5):822-826. doi: 10.1080/10826084.2022.2046090. Epub 2022 Mar 10.
Results Reference
derived
PubMed Identifier
31731006
Citation
Cochran G, Smid MC, Krans EE, Bryan MA, Gordon AJ, Lundahl B, Silipigni J, Haaland B, Tarter R. A pilot multisite study of patient navigation for pregnant women with opioid use disorder. Contemp Clin Trials. 2019 Dec;87:105888. doi: 10.1016/j.cct.2019.105888. Epub 2019 Nov 12.
Results Reference
derived

Learn more about this trial

Optimizing Pregnancy and Treatment Interventions for Moms 2.0

We'll reach out to this number within 24 hrs