- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05552053
Resources, Inspiration, Support and Empowerment (RISE) for Black Pregnant Women (RISE)
Resources, Inspiration, Support and Empowerment (R.I.S.E.) for Black Pregnant Women
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Perinatal mood and anxiety disorders (PMADs) are a leading complication of childbirth with a national prevalence rate of 13%.1-3 This rate triples among Black mothers in Los Angeles (36%)4 who are less likely to receive mental health treatment, particularly during COVID-19.5 Negative impacts of untreated depression or anxiety during pregnancy, coupled with and/or compounded by racism, can include gestational diabetes, prematurity, small gestational age and low birth weight6 - adverse perinatal outcomes (APO) that already disproportionately burden Black women.7-12 The stress of discrimination, worries about adverse outcomes, and APO consequences are thought to increase systemic inflammation,13,14 a mechanism driving mental and physical symptoms. Additionally, research shows that Black patients experience worse communication with their physicians than their white counterparts.15-17 Cultural adaptations to improve communication with providers decrease rates of depression in minority patients18 and improve adherence to insight and alliance.19 In addition to communication barriers and despite recent national recommendations and state laws,20-22 fewer than one in four Los Angeles women receive PMAD screening or education during their prenatal, postpartum or well-child medical visits.23 Based on our team's preliminary data, even when screened many women of color do not respond openly to these questions and few are connected to relevant care.24,25 Finally, a consistent problem is the lack of postpartum follow up for medical and mental health concerns.26 Together the result is a gross lack of referral to appropriate postpartum mental health care and mobile health (mHealth) apps could bridge this divide.
Our community partner Maternal Mental Health NOW developed a Maternal Wellness Self-Help (MWSH) Application that provides PMAD psychoeducation, stress management techniques and tailors a self-help plan for its 700+ users. Given the racial disparities in maternal health it became apparent that content directly addressing the unique cultural needs of Black women was critically needed. Therefore the investigators partnered with Candlelit Therapy, a culturally-relevant, virtual-first telemedicine provider focused on health equity and providing culturally competent behavioral healthcare to change the way Black mothers access perinatal mental healthcare online and get primary care. Candlelit Therapy has developed our intervention, Candlelit Care, which includes three new culturally relevant modules for Black pregnant women to improve (1) self-advocacy skills (2) patient communication with medical providers and (3) provide a support network with other Black pregnant women. In this proposed pilot randomized control trial (RCT) women will be randomized to either the active standard of care control (MWSH) or the standard of care plus the additional modules (MWSH + Candlelit Care).
The proposed pilot RCT will allow the investigators to build on the established MWSH app by adding Candlelit Care, which are culturally relevant modules and to test if it is effective in improving perinatal mental and physical health outcomes among Black Women randomized to the intervention compared to the standard of care control group. Women randomized to the intervention will also have postpartum follow up at regular intervals including additional PMAD screening by a licensed clinician who will provide patient navigation to mental health and/or medical care, if needed. The overarching objective of this research is to improve clinical care of Black women during the perinatal period, with the goal to improve mental health and physical health outcomes. A secondary goal is to identify a plausible biological mechanism through which this intervention is operating.
AIM 1: This RCT will examine the clinical effectiveness of the MWSH App + Candlelit Care intervention at reducing mental and physical health risk. Hypothesis 1a: Compared to a standard of care control group who only receive the MWSH App (N=75) Black pregnant women (N=75) who are randomized to the intervention (MWSH + Candlelit Care), and structured postpartum follow up will have reduced rates of APOs and PMADs. Hypothesis 1b: Among women diagnosed with PMADs, participants in the intervention group will report increased self-advocacy skills, increased communication with providers, and reduced levels of discrimination stress. Participants will also have an increase in adherence to recommended postpartum mental health treatment.
AIM 2: Investigate the physiological mechanisms involved. Hypothesis 2: Black pregnant women who are randomized to MWSH + Candlelit Care (n=25) will have lower circulating inflammation (hs-CRP), and a transcription profile of differentially expressed inflammatory genes, marked by a decreased activity of inflammatory transcription factors NFкB, CREB and JUN compared to the standard MWSH (n=25),
Given the burden of both APOs and PMADs among Black mothers and the numerous consequences on maternal and child outcomes, it is imperative that investigators develop and implement targeted and effective PMAD interventions, and test the biological mechanisms that might drive these effects. This work is translational, builds on a network of community advocates and established clinical providers to implement a novel mHealth intervention informed by real world experiences designed to enhance self-advocacy, reduce stress, and prevent adverse outcomes. This pilot RCT will inform a larger multi-site clinical trial to address mental health disparities in this population.
Study Type
Enrollment (Estimated)
Phase
- Phase 2
- Phase 3
Contacts and Locations
Study Locations
-
-
California
-
Los Angeles, California, United States, 90048
- Cedars Sinai
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Provision of signed and dated informed consent form
- Stated willingness to comply with all study procedures and availability for the duration of the study
- Pregnant Black individuals, at least 18 years of age
- English speaking
- Access to a tablet, smartphone, or computer capable of running the apps
Exclusion Criteria:
- Psychosis
- Perinatal loss
- Individuals outside of the US
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Maternal Wellness Self Help (MWSH) Application
The Maternal Wellness Self Help (MWSH) app was created to help individuals to identify and manage perinatal depression and anxiety.
The app is designed is to meet the emotional needs of those who are pregnant, want to become pregnant or have given birth.
This psycho-educational app informs and normalizes the range of emotional responses throughout the reproductive journey.
By learning about perinatal mental health, this app hopes to empower patients to understand and name their experiences.
|
The Maternal Wellness Self Help (MWSH) app was created to help individuals to manage perinatal depression and anxiety.
The app is designed is to meet the emotional needs of those who are pregnant, want to become pregnant or have given birth.
This psycho-educational app informs and normalizes the range of emotional responses throughout the reproductive journey.
By learning about perinatal mental health, this app hopes to empower patients to understand and name their experiences.
|
|
Experimental: MWSH plus Candlelit Care
Candlelit Care is a virtual perinatal mental health application that builds on cognitive behavioral therapy (CBT) to provide Black, Indigenous and POC women and birthing parents access to culturally affirming mental health support during pregnancy.
Driven by an integrated care team, women have access to self-guided therapeutic tools, peer coaching and education about perinatal mood disorders as a primary resource.
This convenient and trauma informed app allows parents to see if their mental health symptoms warrant further treatment in a secure setting.
The app also provides education of role transitions, discussion of types of interpersonal conflicts common around childbirth (including racial discrimination) and techniques for resolving them, and role-playing with feedback from other parents during groups.
The goals are to improve self-advocacy skills; patient communication with medical providers and provide a support network with other Black pregnant women.
|
Candlelit Care is a virtual perinatal mental health application that builds on cognitive behavioral therapy (CBT) to provide Black, Indigenous and POC women and birthing parents access to culturally affirming mental health support during pregnancy.
Driven by an integrated care team, women have access to self-guided therapeutic tools, peer coaching and education about perinatal mood disorders as a primary resource.
This convenient and trauma informed app allows parents to see if their mental health symptoms warrant further treatment in a secure setting.
The app also provides education of role transitions, discussion of types of interpersonal conflicts common around childbirth (including racial discrimination) and techniques for resolving them, and role-playing with feedback from other parents during groups.
The goals are to improve self-advocacy skills; patient communication with medical providers and provide a support network with other Black pregnant women.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Depression symptoms
Time Frame: 6 months - 1 year
|
Reduced symptoms of depression assessed by the Edinburgh Postnatal Depression Scale (EPDS)
|
6 months - 1 year
|
|
Anxiety symptoms
Time Frame: 6 months - 1 year
|
Reduced symptoms of anxiety assessed by the Overall Anxiety Severity and Impairment Scale (OASIS)
|
6 months - 1 year
|
|
PTSD Symptoms
Time Frame: 6 months - 1 year
|
Reduced symptoms of post-traumatic stress symptoms assessed by the Impact of EVents Scale (IES)
|
6 months - 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Communication
Time Frame: 6 months - 1 year
|
Increased communication with providers assessed by the Communication Assessment Tool (CAT)
|
6 months - 1 year
|
|
Self-Advocacy
Time Frame: 6 months - 1 year
|
Improved self-advocacy skills assessed by the Patient Self-Advocacy Scale (PSAS)
|
6 months - 1 year
|
|
Discrimination stress
Time Frame: 6 months - 1 year
|
Reduced levels of discrimination stress assessed by the Discrimination in Medical Settings (DMS) Scale.
|
6 months - 1 year
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Inflammation
Time Frame: 6 months - 1 year
|
Lower circulating inflammation (hs-CRP), and a transcription profile of differentially expressed inflammatory genes, marked by a decreased activity of inflammatory transcription factors NFкB, CREB and JUN.
|
6 months - 1 year
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Mental Disorders
- Pathologic Processes
- Female Urogenital Diseases and Pregnancy Complications
- Behavioral Symptoms
- Mood Disorders
- Puerperal Disorders
- Depressive Disorder
- Pathological Conditions, Signs and Symptoms
- Behavior
- Social Behavior
- Prejudice
- Social Discrimination
- Anxiety Disorders
- Depression
- Inflammation
- Pregnancy Complications
- Stress, Psychological
- Depression, Postpartum
- Racism
Other Study ID Numbers
- Pro00002283
- 1R21MD017396-01A1 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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