Support program for Black pregnant women facing mental health challenges
Resources, Inspiration, Support and Empowerment (R.I.S.E.) for Black Pregnant Women
This study tests a support program designed to help Black pregnant women with mental health challenges like anxiety and depression to see if it can improve their well-being and communication with healthcare providers.
Quick facts
| Phase | Phase2; Phase3 |
|---|---|
| Study type | Interventional |
| Enrollment | 150 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Cedars-Sinai Medical Center Academic / other |
| Locations | 1 site (Los Angeles, California) |
| Trial ID | NCT05552053 on ClinicalTrials.gov |
What this trial studies
This clinical trial focuses on addressing perinatal mood and anxiety disorders (PMADs) among Black pregnant women, who are disproportionately affected by these conditions. The study aims to implement culturally adapted interventions to improve communication with healthcare providers and reduce the rates of depression and anxiety during pregnancy and postpartum. By utilizing a randomized control trial design, the researchers will evaluate the effectiveness of these interventions in reducing systemic inflammation and improving mental health outcomes. The trial also seeks to connect participants with necessary mental health resources and support.
Who should consider this trial
Good fit: Ideal candidates for this study are Black pregnant individuals aged 18 and older who are English-speaking and have access to a device capable of running the study apps.
Not a fit: Patients with psychosis, perinatal loss, or those located outside of the United States may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve mental health outcomes for Black pregnant women, leading to healthier pregnancies and better overall well-being.
How similar studies have performed: Other studies have shown success with culturally adapted interventions for minority populations, indicating a promising approach to addressing health disparities.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Provision of signed and dated informed consent form 2. Stated willingness to comply with all study procedures and availability for the duration of the study 3. Pregnant Black individuals, at least 18 years of age 4. English speaking 5. Access to a tablet, smartphone, or computer capable of running the apps Exclusion Criteria: 1. Psychosis 2. Perinatal loss 3. Individuals outside of the US
Where this trial is running
Los Angeles, California
- Cedars Sinai — Los Angeles, California, United States (Recruiting)
Study contacts
- Study coordinator: Pearl Heumann, BS
- Email: risestudy@cshs.org
- Phone: 323-866-8107
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.