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Pilot Randomized Controlled Trial (RCT): Remote SBIRT Vs. In-Person SBIRT

Primary Purpose

Pregnancy, Substance Use, Depression

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Listening to Women
Sponsored by
Medical University of South Carolina
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Pregnancy focused on measuring Pregnancy, Depression, Substance Use, Anxiety

Eligibility Criteria

18 Years - 41 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

1) age 18-41; 2) currently pregnant or postpartum; 3) if pregnant, receiving prenatal care; 4) English fluency; 5) owner of a cell phone with short message service (SMS) text-message based capability; 6) access to Wireless Fidelity (WIFI) and a device to allow audio and video teleconferencing; 7) able to provide informed consent.

Exclusion Criteria: None

Sites / Locations

  • Medical University of South Carolina

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Listening to Women

Treatment as Usual

Arm Description

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, other drugs including prescription medication), and domestic violence.

This group will receive in-person screening and referral to treatment assessment. The same screening tools are used to assess substance abuse and mental health problems in LTW and TAU groups.

Outcomes

Primary Outcome Measures

Completion of SBIRT (specific aim 1)
We will compare the proportion of participants that complete a screen for mental health and substance use, the proportion of those screening positive that are referred to treatment, and the proportion of those referred to treatment that had at least one mental health and/or substance use disorder treatment appointment among those assigned to LTW, compared to TAU.
Time to Treatment (specific aim 1)
Time from completion of screening positive to time of first mental health or substance use treatment appointment (if a referral to treatment was appropriate) among those assigned to LTW, compared to TAU.
Change in Mental Health Symptoms (specific aim 1)
Mean change in the Edinburgh Postnatal Depression Scale (EPDS) among women referred for treatment. A score of 10 or more on the Edinburgh Postnatal Depression Scale suggests clinically elevated depressive symptoms requiring further evaluation.
Change in Substance Use (specific aim 1)
Change in substance use frequency and amount as measured by the National Institute on Drug Abuse (NIDA)-Modified Assist among women referred for 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 and a score of 27+ has an indicated response for Brief Intervention (offer options that include treatment).
Change in Maternal Functioning (specific aim 1)
Change in maternal functioning measured by the Medical Outcomes Study Short Form 36 (SF-36v2).
Attendance to Treatment (specific aim 2)
Treatment attendance (defined as attending at least 1 or more visits with a mental health and/or substance use disorder (SUD) treatment provider during pregnancy and the postpartum year)

Secondary Outcome Measures

Recruitment (specific aim 1)
The proportion of patients who agree to participate as compared to the total number solicited to enroll for each recruitment approach
Attrition (specific aim 1)
Proportion of study participants that prematurely terminate i.e., do not complete screenings, or are unable to be contacted for referral and/or treatment.
Study Retention (specific aim 1)
Proportion of study participants that complete all assessment points associated with the protocol.
Treatment Attendance (specific aim 1)
Proportion of participants that attended a mental health or substance use treatment appointment.
Change in Health-Related Social Needs (specific aim 1)
Change in health-related social needs measured by the Accountable Health Communities (AHC) Health-Related Social Needs (HRSN) Screening Tool among those assigned to LTW, compared to TAU
Voice Biomarkers (specific aim 1)
Voice analysis will be completed using an online platform SurveyLex (owned by NeuroLex, Inc.). Among women referred for treatment, we will analyze voice recordings for characteristics (acoustic, linguistic, or meta-feature) which may be compared between those assigned to LTW and those assigned to TAU
Change in Mental Health Symptoms-Depression (specific aim 2)
Among women referred for treatment, we will compare the mean change in the Edinburgh Postnatal Depression Scale (EPDS) among those assigned to LTW, compared to TAU. A score of 10 or more on the Edinburgh Postnatal Depression Scale suggests clinically elevated depressive symptoms requiring further evaluation. A higher score on the EPDS is a worse outcome.
Change in Mental Health Symptoms-Anxiety (specific aim 2)
Among women referred for treatment, we will compare the mean change in the Generalized Anxiety Disorder-7 (GAD-7) among those assigned to LTW, compared to TAU. A score of 1-4 on the GAD-7 indicates minimal anxiety, 5-9 is mild anxiety, 10-14 is moderate anxiety and 15-21 is severe anxiety. A higher score on the GAD-7 is a worse outcome.
Change in Mental Health Symptoms-Suicidal Ideation (specific aim 2)
Among women referred for treatment, we will compare the mean change in the Columbia Suicide Severity Rating Scale (CSSRS) among those assigned to LTW, compared to TAU. There are no specified clinical cutoffs due to the binary nature of the responses to items.
Change in Substance Use-NIDA Modified Assist (specific aim 2)
Among women referred for treatment, we will compare change in substance use frequency and amount as measured by the NIDA-Modified Assist among those assigned to LTW, compared to TAU. 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 and a score of 27+ has an indicated response for Brief Intervention (offer options that include treatment).
Change in Substance Use-Timeline Follow Back (specific aim 2)
Among women referred for treatment, we will compare change in substance use frequency and amount as measured by Timeline Follow-Back (TLFB) among those assigned to LTW, compared to TAU.
Change in Maternal Functioning (specific aim 2)
Among women referred for treatment, we will compare the change in maternal functioning measured by the Medical Outcomes Study Short Form 36 (SF-36v2) among those assigned to LTW, compared to TAU.
Change in Health-Related Social Needs
Among women referred for treatment, we will compare the change in health-related social needs measured by the Accountable Health Communities (AHC) Health-Related Social Needs (HRSN) Screening Tool among those assigned to LTW, compared to TAU.

Full Information

First Posted
November 2, 2020
Last Updated
August 18, 2023
Sponsor
Medical University of South Carolina
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1. Study Identification

Unique Protocol Identification Number
NCT04630249
Brief Title
Pilot Randomized Controlled Trial (RCT): Remote SBIRT Vs. In-Person SBIRT
Official Title
Pilot RCT of Remote Mental Health and Substance Use Screening, Brief Intervention and Referral to Treatment (SBIRT), Compared to In-Person SBIRT for Peripartum Women
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
December 15, 2020 (Actual)
Primary Completion Date
July 21, 2023 (Actual)
Study Completion Date
July 21, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of South Carolina

4. Oversight

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

5. Study Description

Brief Summary
Specific Aim 1: Conduct a pilot, small-scale randomized controlled trial to examine feasibility and preliminary efficacy of LTW, compared to TAU. Outcomes related to feasibility include percentage of eligible patients recruited, study attrition, study retention, and mental health and substance use treatment appointment attendance. Outcomes related to preliminary efficacy will include participation in screening, referral and treatment as well as reduction in mental health and substance use at 1 and 3 months post-study enrollment, compared to TAU. Specific Aim 2: Conduct a randomized controlled trial to examine the effectiveness of LTW, compared to TAU. Outcomes related to effectiveness include attendance to treatment as well as reduction in mental health and substance use at 1 and 3 months post-study enrollment, compared to TAU.
Detailed Description
Participants: 450 adult, pregnant or postpartum women Intervention: Listening to Women is a mobile phone-based program designed to enhance delivery of Screening, Brief Intervention, and Referral to Treatment (SBIRT), an evidence-based approach for mental health and substance use screening and treatment for perinatal women. This program was created as a result of key informant interviews with obstetric providers and pregnant and postpartum women with opioid use disorders. The program utilizes mobile phone 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. Design: Specific aim 1: A two arm pilot RCT (N=100) with 2:1 allocation will examine feasibility and preliminary efficacy of LTW, compared to TAU. Specific aim 2: A RCT (N=350) with 2:1 allocation will examine effectiveness of LTW, compared to TAU. As of the approval of amendment #12 the allocation will switch to 1(LTW):2(TAU) for specific aim 2. This study is part of the HEAL Initiative (https://heal.nih.gov/).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy, Substance Use, Depression, Anxiety
Keywords
Pregnancy, Depression, Substance Use, Anxiety

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
415 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Listening to Women
Arm Type
Experimental
Arm Description
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, other drugs including prescription medication), and domestic violence.
Arm Title
Treatment as Usual
Arm Type
No Intervention
Arm Description
This group will receive in-person screening and referral to treatment assessment. The same screening tools are used to assess substance abuse and mental health problems in LTW and TAU groups.
Intervention Type
Behavioral
Intervention Name(s)
Listening to Women
Intervention Description
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.
Primary Outcome Measure Information:
Title
Completion of SBIRT (specific aim 1)
Description
We will compare the proportion of participants that complete a screen for mental health and substance use, the proportion of those screening positive that are referred to treatment, and the proportion of those referred to treatment that had at least one mental health and/or substance use disorder treatment appointment among those assigned to LTW, compared to TAU.
Time Frame
Screening through 3-months post study enrollment
Title
Time to Treatment (specific aim 1)
Description
Time from completion of screening positive to time of first mental health or substance use treatment appointment (if a referral to treatment was appropriate) among those assigned to LTW, compared to TAU.
Time Frame
Screening through 3-months post study enrollment
Title
Change in Mental Health Symptoms (specific aim 1)
Description
Mean change in the Edinburgh Postnatal Depression Scale (EPDS) among women referred for treatment. A score of 10 or more on the Edinburgh Postnatal Depression Scale suggests clinically elevated depressive symptoms requiring further evaluation.
Time Frame
Change from baseline EPDS at 3-months post study enrollment
Title
Change in Substance Use (specific aim 1)
Description
Change in substance use frequency and amount as measured by the National Institute on Drug Abuse (NIDA)-Modified Assist among women referred for 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 and a score of 27+ has an indicated response for Brief Intervention (offer options that include treatment).
Time Frame
Change from baseline substance use at 3-months post study enrollment
Title
Change in Maternal Functioning (specific aim 1)
Description
Change in maternal functioning measured by the Medical Outcomes Study Short Form 36 (SF-36v2).
Time Frame
Change from baseline maternal functioning at 3-months post study enrollment
Title
Attendance to Treatment (specific aim 2)
Description
Treatment attendance (defined as attending at least 1 or more visits with a mental health and/or substance use disorder (SUD) treatment provider during pregnancy and the postpartum year)
Time Frame
During pregnancy and the postpartum year
Secondary Outcome Measure Information:
Title
Recruitment (specific aim 1)
Description
The proportion of patients who agree to participate as compared to the total number solicited to enroll for each recruitment approach
Time Frame
24 months
Title
Attrition (specific aim 1)
Description
Proportion of study participants that prematurely terminate i.e., do not complete screenings, or are unable to be contacted for referral and/or treatment.
Time Frame
Through study completion, an average of 3 months
Title
Study Retention (specific aim 1)
Description
Proportion of study participants that complete all assessment points associated with the protocol.
Time Frame
Through study completion, an average of 3 months
Title
Treatment Attendance (specific aim 1)
Description
Proportion of participants that attended a mental health or substance use treatment appointment.
Time Frame
Through study completion, an average of 3 months
Title
Change in Health-Related Social Needs (specific aim 1)
Description
Change in health-related social needs measured by the Accountable Health Communities (AHC) Health-Related Social Needs (HRSN) Screening Tool among those assigned to LTW, compared to TAU
Time Frame
Change from baseline Health-Related Social Needs use at 3-months post study enrollment
Title
Voice Biomarkers (specific aim 1)
Description
Voice analysis will be completed using an online platform SurveyLex (owned by NeuroLex, Inc.). Among women referred for treatment, we will analyze voice recordings for characteristics (acoustic, linguistic, or meta-feature) which may be compared between those assigned to LTW and those assigned to TAU
Time Frame
Baseline through 3-months post study enrollment
Title
Change in Mental Health Symptoms-Depression (specific aim 2)
Description
Among women referred for treatment, we will compare the mean change in the Edinburgh Postnatal Depression Scale (EPDS) among those assigned to LTW, compared to TAU. A score of 10 or more on the Edinburgh Postnatal Depression Scale suggests clinically elevated depressive symptoms requiring further evaluation. A higher score on the EPDS is a worse outcome.
Time Frame
Change from baseline mental health symptoms (depression) at 3-months post study enrollment
Title
Change in Mental Health Symptoms-Anxiety (specific aim 2)
Description
Among women referred for treatment, we will compare the mean change in the Generalized Anxiety Disorder-7 (GAD-7) among those assigned to LTW, compared to TAU. A score of 1-4 on the GAD-7 indicates minimal anxiety, 5-9 is mild anxiety, 10-14 is moderate anxiety and 15-21 is severe anxiety. A higher score on the GAD-7 is a worse outcome.
Time Frame
Change from baseline mental health symptoms (anxiety) at 3-months post study enrollment
Title
Change in Mental Health Symptoms-Suicidal Ideation (specific aim 2)
Description
Among women referred for treatment, we will compare the mean change in the Columbia Suicide Severity Rating Scale (CSSRS) among those assigned to LTW, compared to TAU. There are no specified clinical cutoffs due to the binary nature of the responses to items.
Time Frame
Change from baseline mental health symptoms (suicidal ideation) at 3-months post study enrollment
Title
Change in Substance Use-NIDA Modified Assist (specific aim 2)
Description
Among women referred for treatment, we will compare change in substance use frequency and amount as measured by the NIDA-Modified Assist among those assigned to LTW, compared to TAU. 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 and a score of 27+ has an indicated response for Brief Intervention (offer options that include treatment).
Time Frame
Change from baseline substance use at 3-months post study enrollment
Title
Change in Substance Use-Timeline Follow Back (specific aim 2)
Description
Among women referred for treatment, we will compare change in substance use frequency and amount as measured by Timeline Follow-Back (TLFB) among those assigned to LTW, compared to TAU.
Time Frame
Change from baseline substance use at 3-months post study enrollment
Title
Change in Maternal Functioning (specific aim 2)
Description
Among women referred for treatment, we will compare the change in maternal functioning measured by the Medical Outcomes Study Short Form 36 (SF-36v2) among those assigned to LTW, compared to TAU.
Time Frame
Change from baseline maternal functioning at 3-months post study enrollment
Title
Change in Health-Related Social Needs
Description
Among women referred for treatment, we will compare the change in health-related social needs measured by the Accountable Health Communities (AHC) Health-Related Social Needs (HRSN) Screening Tool among those assigned to LTW, compared to TAU.
Time Frame
Change from baseline Health-Related Social Needs use at 3-months post study enrollment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
41 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1) age 18-41; 2) currently pregnant or postpartum; 3) if pregnant, receiving prenatal care; 4) English fluency; 5) owner of a cell phone with short message service (SMS) text-message based capability; 6) access to Wireless Fidelity (WIFI) and a device to allow audio and video teleconferencing; 7) able to provide informed consent. Exclusion Criteria: None
Facility Information:
Facility Name
Medical University of South Carolina
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Pilot Randomized Controlled Trial (RCT): Remote SBIRT Vs. In-Person SBIRT

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