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The DC Mother-Infant Behavioral Wellness Program

Primary Purpose

Perinatal Depression, Perinatal Anxiety, Prenatal Stress

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Patient Navigation
Adapted Cognitive-Behavioral Therapy
Sponsored by
Children's National Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Perinatal Depression focused on measuring Postpartum depression, postpartum anxiety, pregnancy, Black women, stress, Anxiety, Depression

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Black/of African Descent
  • Pregnant (gestational weeks ≤ 28 weeks)
  • Age 18-45
  • English proficient
  • Receiving services in 1 of 4 study sites above
  • Low-income: i.e., receiving Medicaid
  • Subthreshold or threshold risk for maternal distress (stress, depression, and/or anxiety)
  • Able to provide consent

Exclusion Criteria:

  • age <18
  • Currently under the influence of a substance(s)
  • Experiencing psychosis
  • Critical (clinical) risk: actively suicidal or homicidal
  • Not Black/of African Descent
  • Planning to deliver outside DC

Sites / Locations

  • Unity Healthcare - BrentwoodRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Usual Care

Patient Navigation and treatment

Arm Description

Participants will participate in usual prenatal care throughout the duration of study.

In the patient navigation arm, women who do not meet diagnostic criteria (Group 2a) can participate in: (1) group-based CBT preventative intervention; (2) peer support group (virtual); or (3) both. Women in the threshold risk group, meeting diagnostic criteria for depression/anxiety (Group 2b) at baseline can participate in: (1) individual CBT treatment (2) peer support group (virtual) (3) both Prevention group includes 8 sessions based on culturally adapted CBT for Black/ of African descent populations facilitated by mental health professionals. Individual treatment includes 12 sessions based on culturally adapted CBT for Black/ of African descent populations.

Outcomes

Primary Outcome Measures

Change in Stress at 24 weeks of pregnancy to 12 months postpartum
Perceived Stress Scale: A 10-item questionnaire to measure the self-reported level of stress in the respondents by assessing feelings and thoughts during the last month. Each item is scored from 0 (never) to 5 (very often) with a range of 0 to 40 for the total score of the scale. A higher level of stress is indicated by higher scores on this scale.
Change in Depression at 24 weeks of pregnancy to 12 months postpartum
Edinburgh Postnatal Depression Scale: A 10-item scale used to indicate whether a parent has symptoms that are common in women with depression during pregnancy and in the year following the birth of a child. Each item is scored from 0 (As much as I ever did) to 3 (Not at all) with a range of 0 to 30. Higher level of depression is indicated by a higher score on this scale.
Change in Anxiety at 24 weeks of pregnancy to 12 months postpartum
General Anxiety Disorder-7 (GAD-7): A 7-item scale to measure levels of anxiety in respondents by assessing feelings and thoughts over the past 2 weeks. Each item is scored from 0 (Not at all) to 3 (Nearly every day) with a range of 0 to 21. Higher level of depression is indicated by a higher score on this scale.

Secondary Outcome Measures

Full Information

First Posted
March 2, 2022
Last Updated
February 6, 2023
Sponsor
Children's National Research Institute
Collaborators
George Washington University, Patient-Centered Outcomes Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05345834
Brief Title
The DC Mother-Infant Behavioral Wellness Program
Official Title
Advancing Perinatal Mental Health and Well-Being: The DC Mother-Infant Behavioral Wellness Program
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 22, 2022 (Actual)
Primary Completion Date
April 2024 (Anticipated)
Study Completion Date
August 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's National Research Institute
Collaborators
George Washington University, Patient-Centered Outcomes Research Institute

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
This randomized controlled study will examine the effectiveness of patient navigation with culturally adapted cognitive-behavioral interventions and peer support groups for low-income Black/of African Descent pregnant women who are experiencing stress, anxiety, and/or depression.
Detailed Description
The overarching objective is to develop and evaluate a collaborative, multi-dimensional and culturally tailored community-based model of integrated perinatal MH care. The target population is low-income Black/of African descent women with pregnancy-related stress, anxiety, and depression. There are two specific aims: (1) to refine an individualized plan to integrate patient navigation and a culturally adapted cognitive-behavioral (CBT) intervention for low-income Black/of African Descent women designed to increase recruitment and retention within the healthcare community system, and (2) through a two-arm prospective randomized controlled design, women who are subthreshold and threshold risk for prenatal stress, depression and/or anxiety will participate in one of two interventions: (a) existing prenatal intervention (usual care); or (b) patient navigation plus culturally adapted CBT, and peer support groups. The investigators will screen 1,000 low-income pregnant AA women (18-45 years of age) in their second pregnancy visit with validated tools for stress, anxiety, and depression. A total of 700 study participants will be recruited from urban prenatal care centers in the Washington DC area and will be randomized Usual Care of Intervention conditions above (n=350/condition). Following randomization, participants will participate in a diagnostic interview based on DSM-5 criteria to 'self-select' themselves into 1 of 2 groups (i.e., 'threshold' or 'subthreshold'). Threshold includes women who meet criteria for depression or anxiety based on DSM-5 diagnostic criteria. Subthreshold includes all other women who do not meet DSM criteria). In the intervention arm, participants in the threshold group will receive a 1:1 CBT treatment intervention, and participants in the subthreshold group will receive a group CBT intervention. Both threshold groups will also include patient navigation and participation in a peer support group. Participants will complete standardized health, mental health, and well-being questionnaires during pregnancy at their prenatal site, and up to 12 months after delivery at their well-baby visits, when they also will complete questionnaires about their infants' development and behavior. All infants also will undergo a standardized developmental test at 12 months. Health care utilization and outcomes also will be collected through electronic medical records.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Perinatal Depression, Perinatal Anxiety, Prenatal Stress
Keywords
Postpartum depression, postpartum anxiety, pregnancy, Black women, stress, Anxiety, Depression

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Women in the patient navigator arm (Group 2a) can choose to participate in group-based preventive interventions based on: (1) a culturally adapted CBT (in person within prenatal care site or virtual given COVID); (2) peer support group (virtual); or (3) both. Women in the threshold risk group (Group 2b) at baseline warrant treatment interventions and will be invited to participate in: (1) culturally adapted CBT (individual, in person or virtual given COVID); (2) peer support (virtual); or (3) both. Women in this more severe risk group may be referred for psychiatric treatment if warranted. Randomization lists will be generated by the study statistician using a permuted block design and uploaded to a HIPAA-compliant, password-protected website (REDCap) allowing for patient randomization at the time of registration in the data collection system.
Masking
None (Open Label)
Masking Description
None (Open Label)
Allocation
Randomized
Enrollment
700 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Participants will participate in usual prenatal care throughout the duration of study.
Arm Title
Patient Navigation and treatment
Arm Type
Experimental
Arm Description
In the patient navigation arm, women who do not meet diagnostic criteria (Group 2a) can participate in: (1) group-based CBT preventative intervention; (2) peer support group (virtual); or (3) both. Women in the threshold risk group, meeting diagnostic criteria for depression/anxiety (Group 2b) at baseline can participate in: (1) individual CBT treatment (2) peer support group (virtual) (3) both Prevention group includes 8 sessions based on culturally adapted CBT for Black/ of African descent populations facilitated by mental health professionals. Individual treatment includes 12 sessions based on culturally adapted CBT for Black/ of African descent populations.
Intervention Type
Behavioral
Intervention Name(s)
Patient Navigation
Other Intervention Name(s)
Maternity Care Specialist
Intervention Description
Participants in arm 2 will receive patient navigation provided by humans (rather than e-navigation) to provide personalized care to include support, resources, and referrals to address psychosocial issues that arise during the perinatal period. Patient navigation is available to participants through 12 months postpartum.
Intervention Type
Behavioral
Intervention Name(s)
Adapted Cognitive-Behavioral Therapy
Other Intervention Name(s)
Adapted CBT
Intervention Description
Participants who do not meet diagnostic criteria (Group 2a) will participate in a prevention group which includes 8 sessions based on culturally adapted CBT for Black/ of African descent populations facilitated by mental health professionals. Participants who meet diagnostic criteria (Group 2b) will participate in individual treatment which includes 12 sessions based on culturally adapted CBT for Black/ of African descent populations.
Primary Outcome Measure Information:
Title
Change in Stress at 24 weeks of pregnancy to 12 months postpartum
Description
Perceived Stress Scale: A 10-item questionnaire to measure the self-reported level of stress in the respondents by assessing feelings and thoughts during the last month. Each item is scored from 0 (never) to 5 (very often) with a range of 0 to 40 for the total score of the scale. A higher level of stress is indicated by higher scores on this scale.
Time Frame
Stress will be measured at 24 weeks of pregnancy through infant age of 12 months
Title
Change in Depression at 24 weeks of pregnancy to 12 months postpartum
Description
Edinburgh Postnatal Depression Scale: A 10-item scale used to indicate whether a parent has symptoms that are common in women with depression during pregnancy and in the year following the birth of a child. Each item is scored from 0 (As much as I ever did) to 3 (Not at all) with a range of 0 to 30. Higher level of depression is indicated by a higher score on this scale.
Time Frame
2nd Obstetrics visit (assessed 24-28 weeks gestation) through 12 months postpartum
Title
Change in Anxiety at 24 weeks of pregnancy to 12 months postpartum
Description
General Anxiety Disorder-7 (GAD-7): A 7-item scale to measure levels of anxiety in respondents by assessing feelings and thoughts over the past 2 weeks. Each item is scored from 0 (Not at all) to 3 (Nearly every day) with a range of 0 to 21. Higher level of depression is indicated by a higher score on this scale.
Time Frame
2nd Obstetrics visit (assessed 24-28 weeks gestation) through 12 months postpartum

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Black/of African Descent Pregnant (gestational weeks ≤ 28 weeks) Age 18-45 English proficient Receiving services in 1 of 4 study sites above Low-income: i.e., receiving Medicaid Subthreshold or threshold risk for maternal distress (stress, depression, and/or anxiety) Able to provide consent Exclusion Criteria: age <18 Currently under the influence of a substance(s) Experiencing psychosis Critical (clinical) risk: actively suicidal or homicidal Not Black/of African Descent Planning to deliver outside DC
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Huynh-Nhu Le, PhD
Phone
(202) 994-6808
Email
hnle@gwu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Kiara A Barnett, M.Ed
Phone
9176792151
Email
kabarnett@gwu.edu
Facility Information:
Facility Name
Unity Healthcare - Brentwood
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20018
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Siobhan Burke, MD
Email
sburke@unityhealthcare.org
First Name & Middle Initial & Last Name & Degree
Maariya Bassa, CNM
Email
mbassa@unityhealthcare.org

12. IPD Sharing Statement

Learn more about this trial

The DC Mother-Infant Behavioral Wellness Program

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