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This is randomized control trial of a brief intervention called Bellevue ROSE (Reach Out Stay Strong Essentials). Bellevue ROSE is a manualized and highly structured interpersonal intervention that provides women with psycho-education about maternal depression and strategies for strengthening social support and connectedness. Investigators use motivational interviewing strategies to improve treatment compliance and resource acquisition
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| High Risk PTSD Group 1 | Active Comparator | Forty women who are eligible for the study will be randomized into either the Bellevue ROSE intervention (treatment group) or a psycho-education session and usual, standard of care (control group 1) |
|
| High Risk PTSD Group 2 | Active Comparator | Forty women who are eligible for the study will be randomized into either the Bellevue ROSE intervention (treatment group) or a psycho-education session and usual, standard of care (control group 1) |
|
| Low Risk PTSD Control | Experimental | Twenty additional women, who are at lower risk and thus not eligible for randomization, will also receive one psycho-education session and usual care (control group 2). |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Bellevue ROSE Intervention | Behavioral |
| ||
| Psycho-education session and usual, Standard of care Control |
| Measure | Description | Time Frame |
|---|---|---|
| Depression severity measured by Patient Health Questionnaire (PHQ-9) | 6 Months | |
| Measure of psycho social risk assessment according to Adapted antenatal Risk Questionnaire (ANRQ) | Screening | |
| Measure of perceived social support measured by Multidimensional Scale of Perceived Social Support (MSPSS) | 6 Months | |
| Measure of stress using Perceived Stress Index (PSS) | 6 Months | |
| Parenting Practices and treatment assessed by Parenting Practices and Treatment Questionnaire | 6 Months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Bonnie Kerker, MD | New York University Medical School | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| New York University School of Medicine | New York | New York | 10016 | United States |
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| ID | Term |
|---|---|
| D019052 | Depression, Postpartum |
| ID | Term |
|---|---|
| D011644 | Puerperal Disorders |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
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| Behavioral |
Psycho Education and usual, standard of care |
|
| One Psycho-education session and usual, standard of care Control | Behavioral |
|
| D003866 | Depressive Disorder |
| D019964 | Mood Disorders |
| D001523 | Mental Disorders |