Improving Maternal Mental Health & SUD Screening and Treatment

Sponsor
Medical University of South Carolina (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05764213
Collaborator
(none)
9,444
2
30

Study Details

Study Description

Brief Summary

The purpose of the study is to compare a text message-based mental health and substance use screening and referral to a treatment program, called Listening to Women and Pregnant and Postpartum People (LTWP), to standard of care in-person mental health and substance use screening to look at rates of treatment attendance and retention in treatment. Participation would involve completing online questionnaires. You may be eligible to participate if you are age 18-45 years, are pregnant and entering prenatal care in one of MUSC's OB clinics, and attended a prenatal appointment at an MUSC clinic.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Listening to Women & Postpartum People
N/A

Detailed Description

Aim 1: To determine differences in rates of treatment attendance and retention for Perinatal Mood and Anxiety Disorders (PMADs) and Perinatal Substance Use Disorders (PSUDs) between participants assigned to LTWP, compared to SBIRT.

Aim 2: To determine differences in Patient-Reported Outcomes (PROs) including depressive symptoms, quality of life, substance use, and maternal functioning and well-being measured at the time of referral (baseline=0) and 2, 5, 8, and 11 months postpartum.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
9444 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Screening
Official Title:
Improving Maternal Mental Health & Substance Use Disorder Screening and Treatment
Anticipated Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Jul 31, 2025
Anticipated Study Completion Date :
Oct 1, 2025

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Screening Brief Intervention & Referral to Treatment (SBIRT)

This group will receive in-person screening and referral to treatment assessment.

Experimental: Listening to Women & Pregnant & Postpartum People (LTWP)

This group will receive text-message-based SBIRT with phone-based assessment and referral to treatment. The SBIRT is a survey with 9 questions related to depression, anxiety, substance abuse (alcohol, cigarettes, and other drugs including prescription medication), and domestic violence.

Behavioral: Listening to Women & Postpartum People
Participants are enrolled in text message-based screenings with immediate automated feedback, paired with remote care coordination and, if appropriate, home-based telemedicine mental health and substance use disorder treatment services.

Outcome Measures

Primary Outcome Measures

  1. Change in Treatment Attendance [Through participants baseline prenatal care appointment and pregnancy in the postpartum year for participants, approximately 21 months]

    Treatment attendance is defined as attending at least 1 or more visits with a mental health or substance use disorder treatment provider.

  2. Change in Retention in Treatment [Through participants baseline prenatal care appointment and pregnancy in the postpartum year for participants, approximately 21 months]

    Retention in treatment are PMADs: defined as 6 or more psychotherapy visits and/or 4 or more medication management visits; PSUDs: are defined as continuous pharmacological and/or behavioral treatment > 2 months.

Secondary Outcome Measures

  1. Change in depressive symptoms [Change from baseline depression screening symptoms to follow-up depression screening symptoms during the postpartum year, approximately over 21 months.]

    We will compare the mean change in the Edinburgh Postnatal Depression Scale (EPDS) among those assigned to LTWP compared to SBIRT. A score of 10 or more on the EPDS suggests clinically elevated depressive symptoms requiring further evaluation. A score of 10 or more on the EPDS suggests clinically elevated depressive symptoms requiring further evaluation. A higher score on the EPDS is a worse outcome.

  2. Change in Substance Use [Change from baseline substance use to follow-up substance use during the postpartum year, approximately over 21 months.]

    We will compare the change in substance use frequency and amount as measured by the ASSIST among those assigned to LTWP compared to SBIRT. A score of 0-3 (0-4 for cannabis) has an indicated response for brief education, a score of 4-26 (5-26 for cannabis) has an indicated response for brief intervention, a score of 27+ has an indicated response for brief intervention (offer options that include treatment).A score of 0-3 (0-4 for cannabis) has an indicated response for brief education, a score of 4-26 (5-26 for cannabis) has an indicated response for brief intervention, a score of 27+ has an indicated response for brief intervention (offer options that include treatment).

  3. Change in Maternal Functioning and Wellbeing [Change from baseline maternal functioning to follow-up maternal functioning during the postpartum year, approximately over 21 months.]

    We will compare the change in maternal functioning measured by the Barkin Index of Maternal Functioning among those assigned to LTWP compared to SBIRT. Each item is rated on a 7-point likert scale ranging from 0 = "strongly disagree" to 6 = "strongly agree". The total score ranges from 0 to 120. Higher levels of functioning are associated with higher total scores with 120 representing optimal functioning. Lower levels of functioning are associated with lower scores.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Aim 1:

This study is a cluster RCT step wedge design so we are randomizing on the clinic level, not the individual level. The clinics are made up of 4 "wedges" (3 clinics/wedge). Pregnant women receiving prenatal care in these clinics will receive SBIRT as part of usual care. Clusters of clinics will be randomized to an LTWP start date where they will transition from SBIRT to LTWP for the purposes of screening and referral to treatment.

EHR Data Collection (PPP):
Inclusion:
  1. Age 18-45

  2. pregnant and entering prenatal care in one of MUSC's OB clinics

  3. attended a prenatal appointment at an MUSC clinic

Exclusion:

None

Aim 2:
Study Assessments at baseline and 2, 5, 8, and 11 months postpartum (PPP):
Inclusion:
  1. Age 18-45 years

  2. pregnant

  3. attended an initial prenatal appointment at an MUSC OB clinic

Exclusion:

a.) Unable to complete study assessments

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Medical University of South Carolina

Investigators

  • Principal Investigator: Constance Guille, MD, Medical University of South Carolina

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Constance Guille, Professor, Medical University of South Carolina
ClinicalTrials.gov Identifier:
NCT05764213
Other Study ID Numbers:
  • 00123833
First Posted:
Mar 10, 2023
Last Update Posted:
Mar 17, 2023
Last Verified:
Mar 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 17, 2023