Collaborative Care Model for Perinatal Mental Health
Collaborative Care Model for Perinatal Wellness Support Services - Population-Level Equity-Centered Systems Change
Recruiting
N/AInterventional Study
Perinatal Mental Health
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Health Services Research
Participants needed
14,820 (estimated)
Sponsor
Women and Infants Hospital of Rhode Island · Other
Who this trial is looking for
This trial is looking for pregnant and postpartum people who are at least 20 weeks along in their pregnancy. Participants will help evaluate a new support program aimed at improving mental health during this period.
Are You a Good Fit for This Trial?
You may be able to join if
I am pregnant or postpartum.
I am at least 20 weeks pregnant.
I am over 17 years old.
You may not be able to join if
I am under 18 years old.
I am not at least 20 weeks pregnant.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The collaborative care model (CCM) is a health services intervention that integrates mental health care in primary care settings. The goal of this study is to adapt the CCM to the perinatal care context, including community co-designed adaptations to enhance health equity (COMPASS+). The main objectives of the study are to:
1. Evaluate the effect of COMPASS+ on depression symptom outcomes. Specif…
The collaborative care model (CCM) is a health services intervention that integrates mental health care in primary care settings. The goal of this study is to adapt the CCM to the perinatal care context, including community co-designed adaptations to enhance health equity (COMPASS+). The main objectives of the study are to:
1. Evaluate the effect of COMPASS+ on depression symptom outcomes. Specifically we will evaluate population-level depression symptom trajectories and the prevalence of suicidal ideation among. We will also measure rates of depression response and remission for those who have elevated screen scores (i.e., PHQ9 ≥ 10)
2. Adapt, optimize, and evaluate COMPASS+ implementation strategies to the unique context of perinatal care and evaluate implementation outcomes. The RE-AIM framework will be used to evaluate implementation outcomes (acceptability, appropriateness, feasibility, and fidelity). We hypothesize that variability in effectiveness outcomes will be attributable to variability in fidelity to the implementation strategies or in implementation outcomes.
3. Identify the effect of COMPASS+ on perinatal depression and implementation outcomes across racial and ethnic subgroups.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* all pregnant and postpartum people receiving care at participating sites, who reach a gestational age of 20 or more weeks
* age \> 17 years
Exclusion Criteria:
* age \< 18 years
* all pregnant and postpartum people receiving care at participating sites, who do not reach a ge…
Inclusion Criteria:
* all pregnant and postpartum people receiving care at participating sites, who reach a gestational age of 20 or more weeks
* age \> 17 years
Exclusion Criteria:
* age \< 18 years
* all pregnant and postpartum people receiving care at participating sites, who do not reach a gestational age of 20 or more weeks
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