No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
16 (estimated)
Sponsor
Northwestern University · Other
Who this trial is looking for
This trial is looking for LGBTQ+ individuals who are pregnant or have recently given birth and are experiencing mild depressive symptoms. Participants will help test a program aimed at preventing perinatal depression and share their experiences with it.
Are You a Good Fit for This Trial?
You may be able to join if
I self-identify as LGBTQ+
I am 18 years old or older
I live in the USA or territories
I speak and understand English
I am currently pregnant or within one year of childbirth
I have mild depressive symptoms or risk factors for postpartum depression
You may not be able to join if
I am unable to consent or have impaired decision-making capacity
I have current suicidal or homicidal thoughts
I am experiencing active psychosis or mania
I am having a severe depressive episode
I do not have the ability to use audio or video for remote group sessions
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 goal of this study will be piloting the Parents and Babies perinatal depression prevention intervention to examine its feasibility and acceptability and to obtain preliminary data on its efficacy. This includes exploring/understanding users' experiences navigating the interventions (e.g., from an implementation perspective) and preliminary evaluations of clinical outcomes, including mental hea…
The goal of this study will be piloting the Parents and Babies perinatal depression prevention intervention to examine its feasibility and acceptability and to obtain preliminary data on its efficacy. This includes exploring/understanding users' experiences navigating the interventions (e.g., from an implementation perspective) and preliminary evaluations of clinical outcomes, including mental health and minority stress. With data gathered from this pilot study, we will make final adaptations to the Parents and Babies manuals and plan to develop a randomized-control trial to evaluate efficacy of the intervention.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* self-identify as LGBTQ+
* 18 years old or older
* live in the USA or territories
* speak and understand English
* Currently pregnant or within one year of childbirth
* Endorse current mild depressive symptoms or risk factors for postpartum depression
Exclusion Criteria:
* Ar…
Inclusion Criteria:
* self-identify as LGBTQ+
* 18 years old or older
* live in the USA or territories
* speak and understand English
* Currently pregnant or within one year of childbirth
* Endorse current mild depressive symptoms or risk factors for postpartum depression
Exclusion Criteria:
* Are unable to consent/have impaired decision making capacity
* Have current active suicidal or homicidal ideation, active psychosis, or current mania
* Are currently experiencing a severe depressive episode
* Do not have audio and/or video capacity for attending group sessions remotely.
Contacts
No contact information available.
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