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Prevention study for Postpartum Depression
Official title The ROSE Scale-up Study: Informing a Decision About ROSE as Universal PPD Prevention
ClinicalTrials.gov ID: NCT05700760
What this study is testing
- What it's testing
- The Reach Out, Stand Strong, Essentials for New Mothers (ROSE) program is an evidence-based intervention that prevents half of cases of postpartum depression and was one of two interventions recommended by the US Preventive Services Task Force in 2019. All effectiveness trials of ROSE and of the other recommended PPD prevention intervention included only low-income women a single risk factor that doubles incidence of PPD.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older, women only. Healthy volunteers may be eligible.
You may be able to join if
- Is aged 18 or older
- Is receiving prenatal services within the U.S
- Is between 12-32 weeks pregnant
- Speaks and understand English well enough to understand questionnaires when they are read aloud
- Has access to a telephone through owning one, a relative/friend, or an agency
You likely can't join if
- Has a current major depressive episode
- Has current or past diagnosis of a bipolar disorder or a psychotic disorder
See the full eligibility criteria
- Is aged 18 or older
- Is receiving prenatal services within the U.S
- Is between 12-32 weeks pregnant
- Speaks and understand English well enough to understand questionnaires when they are read aloud
- Has access to a telephone through owning one, a relative/friend, or an agency
- Is willing and able to provide the name and contact information of at least two locator persons
- Has a current major depressive episode
- Has current or past diagnosis of a bipolar disorder or a psychotic disorder
The study team makes the final eligibility decision.
Where it's taking place
- Flint, Michigan, United States
Compensation & support
A stipend or compensation may be offered.
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Flint, Michigan, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.