Comparing the Effectiveness of Clinicians and Paraprofessionals to Reduce Disparities in Perinatal Depression
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ClinicalTrials.gov Identifier: NCT02979444 |
Recruitment Status :
Completed
First Posted : December 1, 2016
Results First Posted : April 13, 2020
Last Update Posted : October 5, 2020
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Condition or disease | Intervention/treatment | Phase |
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Perinatal Depression PostPartum Depression | Behavioral: Mothers and Babies Groups | Not Applicable |

Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 874 participants |
Allocation: | Randomized |
Intervention Model: | Factorial Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Prevention |
Official Title: | Comparing the Effectiveness of Clinicians and Paraprofessionals to Reduce Disparities in Perinatal Depression |
Study Start Date : | August 2016 |
Actual Primary Completion Date : | August 5, 2019 |
Actual Study Completion Date : | August 13, 2020 |

Arm | Intervention/treatment |
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Experimental: Mothers and Babies Groups Home-Visitor
Women who participate in the home-visitor led arm will receive the intervention from a paraprofessional home-visitor and complete assessments at baseline, post-intervention, and 12 and 24 weeks postpartum.
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Behavioral: Mothers and Babies Groups
The Mothers and Babies group intervention is comprised of 6, two hour sessions. It is divided into three overall sections, one on each of the following Cognitive Behavioral Theory components; Pleasant Activities, Thoughts, and Contact with Others. In each of these sections, participants are first taught to understand how the component influences her mood. This teaching of the relationships between CBT components and mood is referred to as psychoeducation. In addition to psychoeducation, participants also receive concrete skills in each of the three sections (pleasant activities, thoughts, contact with others). These skills are intended to provide participants with a "toolkit" of approaches they can use to improve their mood. |
Experimental: Mothers and Babies Groups Clinician
Women who participate in the mental health consultant led arm will receive the intervention from a mental health consultant and complete assessments at baseline, post-intervention, and 12 and 24 weeks postpartum.
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Behavioral: Mothers and Babies Groups
The Mothers and Babies group intervention is comprised of 6, two hour sessions. It is divided into three overall sections, one on each of the following Cognitive Behavioral Theory components; Pleasant Activities, Thoughts, and Contact with Others. In each of these sections, participants are first taught to understand how the component influences her mood. This teaching of the relationships between CBT components and mood is referred to as psychoeducation. In addition to psychoeducation, participants also receive concrete skills in each of the three sections (pleasant activities, thoughts, contact with others). These skills are intended to provide participants with a "toolkit" of approaches they can use to improve their mood. |
No Intervention: Control
Women who participate in the control arm will not receive the intervention but will complete assessments at baseline, 8 weeks post-baseline, and 12 and 24 weeks postpartum.
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- The Change in QIDS-16 Scores From Baseline to 24 Weeks Postpartum [ Time Frame: Baseline and 12 and 24-week postpartum follow-up ]Quick Inventory of Depressive Symptomatology-Self-Report (QIDS-SR16). The QIDS-SR16 was used to assess severity of depressive symptoms consistent with Diagnostic and Statistical Manual symptom criteria. Total scores range from 0-27; higher scores indicate greater symptomatology. The investigators anticipate a clinically meaningfully difference to be on the order of five points (as this is the difference in score on each severity level of depression) (Trivedi et al., 2004). For our non-inferiority analyses comparing MB led by home visitors vs. MB led by mental health clinicians, we will have >85% power to detect a difference difference in mean QIDS-16 scores of two points between the two active intervention arms.
- The Change in the Behavioral Activation Scale From Baseline to 24-weeks Postpartum [ Time Frame: Baseline and 12 and 24-week postpartum follow-ups ]Behavioral Activation will be measured using the Behavioral Activation Depression Scale (BADS). The BADS assesses behaviors hypothesized to underlie depression and specifically targeted for change by behavioral activation strategies. It examines changes in the following areas: activation, avoidance/ rumination, work/school impairment, and social impairment. The BADS consists of 25 items, each rated on a seven point scale ranging from 0 (not at all) to 6 (completely). The range of the scale is 0-64. For the total scale, higher scores represent increased activation. The BADS has demonstrated strong internal consistency, construct validity, and predictive validity (Kanter et al, 2007; Kanter et al., 2009).
- The Change in the Negative Mood Regulation Scale [ Time Frame: Baseline and 12 and 24-week postpartum follow-ups ]Mood regulation will be measured using the 30-item Negative Mood Regulation Scale (NMRS) (Catanzaro & Means, 1990). For each question, respondents use a 5-point scale to indicate what they believe they can do when they are disappointed or experiencing a negative mood. For our analyses, these items were averaged to create a mean NMRS score (range 1-5). Higher scores indicate a greater ability to regulate one's mood.
- The Change in the MOS Social Support Survey From Baseline to 24-Weeks Postpartum [ Time Frame: Baseline and 12 and 24-week follow-ups ]Social support will be measured using the 19-item Medical Outcomes Study Social Support Survey (MOS-SSS) (Sherbourne & Stewart, 1991). This brief self-administered survey includes an overall functional social support index, as well as four functional support subscales: affectionate, emotional/informational, tangible, and positive social interaction. The range is 1-5 with greater scores indicating more perceived social support.
- The Change in the Experiences Questionnaire From Baseline to 24-Weeks Postpartum [ Time Frame: Baseline and 12 and 24-week follow-ups ]Decentering will be measured using the Experiences Questionnaire (EQ) (Fresco et al., 2007). The EQ is a 20 item self-report scale designed to measure decentering and rumination, which has demonstrated strong internal consistency in a number of studies examining effects of interventions that incorporate cognitive restructuring techniques. Response choices are on a 1-5 scale. For the purposes of our analyses, we created a mean EQ score (range 1-5), with higher scores indicating more decentering/rumination.

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Ages Eligible for Study: | 16 Years and older (Child, Adult, Older Adult) |
Sexes Eligible for Study: | Female |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- The investigators will enroll only pregnant women in this study, given that the Mothers and Babies Course is delivered prenatally as a postpartum depression prevention intervention. The investigators will offer participation to prenatal home visiting clients, ages 16 and older, knowing the client base for home visiting programs includes pregnant teens.
Exclusion Criteria:
- Women with high-risk medical and pregnancy conditions will be excluded since this may preclude women from regularly attending intervention sessions. The investigators will not exclude women based on race/ethnicity or based on demographic characteristics other than the ability to speak English or Spanish.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02979444
United States, Illinois | |
Northwestern University | |
Chicago, Illinois, United States, 60611 |
Principal Investigator: | Darius Tandon, PhD | Northwestern University |
Documents provided by Darius Tandon, Northwestern University:
Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Darius Tandon, Associate Professor, Northwestern University |
ClinicalTrials.gov Identifier: | NCT02979444 |
Other Study ID Numbers: |
STU00203761 |
First Posted: | December 1, 2016 Key Record Dates |
Results First Posted: | April 13, 2020 |
Last Update Posted: | October 5, 2020 |
Last Verified: | September 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Depression, Postpartum Asphyxia Neonatorum Depression Depressive Disorder Behavioral Symptoms |
Mood Disorders Mental Disorders Puerperal Disorders Pregnancy Complications Infant, Newborn, Diseases |