Parenting Skills Group for Mothers With Postpartum Depression
University of Colorado, Denver · NCT05772897
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–50 · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 750
- US sites recruiting
- 1
- Study start
- August 3, 2023
- Record last updated
- November 30, 2023
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of this longitudinal study is to study the effects of a parenting skills group (Circle of Security Parenting, aka COSP) in mothers with postpartum depression. The main questions it aims to answer are:
- Will changes in methylation of the OXTR rs53576 be apparent in mother and/or infant after having gone through the 8-week COSP program?
- Will COSP participation be associated with improved symptoms of postpartum depression (over and above standard care), attachment style, and relational characteristics of the mother-infant dyad?
- Will COSP participation be associated with changes in social behavior in the infant, and if so, do they persist throughout childhood?
Participants will
- Participate in an 8-week COSP program delivered remotely via Zoom.
- Provide buccal swabs (mother and infant) to assess changes in methylation of OXTR rs53576 pre- versus post-intervention.
- Complete a series of assessment questionnaires delivered remotely.
- Videotape a play-based assessment in their home.
- Receive infant developmental testing
Researchers will compare characteristics of waitlist controls to those participating in the COSP program at the mid-way point of the program to see if the two groups differ.
Being studied: Circle of Security Parenting program
Conditions: Postpartum Depression
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Mothers aged 18-50 years old with infants aged 3-14 months old
- Mothers who are experiencing symptoms of depression and mothers who are not experiencing symptoms of depression (non-depressed controls) are encouraged to participate.
(please note that mothers who are experiencing active depression and who are not already being treated under the care of a qualified healthcare provider (i.e. through therapy or psychopharmacological intervention) will be referred for such treatment prior to being enrolled in the study. This study is not a replacement for professional management of depression or other mental health symptoms.
Exclusion Criteria
- Mothers with severe psychopathology (such as bipolar disorder, schizophrenia, personality disorders, among others)
- Infants with major medical problems that may interfere with a mother's ability to participate in and benefit from the intervention
Recruiting US locations
University of Colorado Denver
Denver, CO 80204
Site contact: Sunny Stophaeros, MS · 925-339-2971 · sunny.stophaeros@ucdenver.edu
Study contacts (from the official record)
- Sunny Stophaeros, MS · 9253392971 · sunny.stophaeros@ucdenver.edu
- Caroline R Harrison, MPH · caroline.harrison@cuanschutz.edu
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