Post-partum Depression
Conditions
Keywords
psycho-education, maternal depression, Reach Out Stay Strong Essentials
Brief summary
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
Interventions
BEHAVIORALBellevue ROSE Intervention
BEHAVIORALPsycho-education session and usual, Standard of care Control
Psycho Education and usual, standard of care
BEHAVIORALOne Psycho-education session and usual, standard of care Control
Sponsors
NYU Langone Health
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Caregiver, Investigator)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No
Inclusion criteria
* English speaking * Women who score between 5-19 on the PHQ-9 and \>23 on the ANRQ
Exclusion criteria
* Women who score \<5 or \>19 on the PHQ-9 * Women who are currently suicidal, active substance users, currently experiencing domestic violence, or have a current or past history of bipolar or psychotic disorder diagnosis. * Women who are currently in treatment for psychotherapy. * Unable to speak and/or understand English proficiently * Unable to provide informed consent
Design outcomes
Primary
| Measure | 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 |
Countries
United States
Outcome results
None listed