Parenting skills program for mothers with postpartum depression
Effects of Attachment-Focused Parenting Intervention on Postpartum Depression and Biological Markers of Stress in Mothers and Their Infants
NA · University of Colorado, Denver · NCT05772897
This study tests whether a parenting skills program can help mothers with postpartum depression feel better and improve their relationship with their babies.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 750 (estimated) |
| Ages | 18 Years to 50 Years |
| Sex | Female |
| Sponsor | University of Colorado, Denver (other) |
| Locations | 1 site (Denver, Colorado) |
| Trial ID | NCT05772897 on ClinicalTrials.gov |
What this trial studies
This longitudinal study investigates the effects of the Circle of Security Parenting (COSP) program on mothers experiencing postpartum depression. Over an 8-week period, participants will engage in remote sessions via Zoom, providing biological samples and completing assessments to evaluate changes in maternal depression symptoms, attachment styles, and infant social behaviors. The study aims to explore the biological mechanisms related to oxytocin receptor gene methylation and the impact of secure attachment on mother-infant relationships. Data will be collected at multiple time points to assess the efficacy of the intervention.
Who should consider this trial
Good fit: Ideal candidates are mothers aged 18-50 with infants aged 3-14 months, experiencing symptoms of postpartum depression or serving as non-depressed controls.
Not a fit: Patients with severe mental health issues or infants with major medical problems may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve maternal mental health and enhance the mother-infant bond.
How similar studies have performed: Other studies have shown promising results with similar parenting interventions, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Denver, Colorado
- University of Colorado Denver — Denver, Colorado, United States (RECRUITING)
Study contacts
- Principal investigator: Sunny Stophaeros, MS — sunny.stophaeros@ucdenver.edu
- Study coordinator: Sunny Stophaeros, MS
- Email: sunny.stophaeros@ucdenver.edu
- Phone: 9253392971
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Postpartum Depression