Screening for postpartum anxiety and related conditions in new parents
Postpartum Screening for Anxiety and Comorbid Conditions: A Prospective British Columbia Cohort Study
University of British Columbia · NCT06242717
This study is trying to find better ways to check for anxiety and related issues in new parents in British Columbia by having them fill out questionnaires online after they have their babies.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 550 (estimated) |
| Ages | 19 Years and up |
| Sex | Female |
| Sponsor | University of British Columbia (other) |
| Locations | 1 site (Vancouver, British Columbia) |
| Trial ID | NCT06242717 on ClinicalTrials.gov |
What this trial studies
This project aims to develop personalized screening strategies for postpartum anxiety and related conditions in British Columbia, Canada. A cohort of 550 postpartum individuals will complete seven questionnaires designed to assess anxiety, depression, social support, pain, quality of life, and sleep disturbances at 4-8 weeks after delivery. The study will evaluate the feasibility of using a web-based platform for screening and will include follow-up interviews to assess usability and participant experiences.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 19 and older who are 4-8 weeks postpartum and proficient in English, having delivered within British Columbia.
Not a fit: Patients who are not proficient in English or who delivered outside of British Columbia may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved identification and management of postpartum anxiety and related conditions, enhancing the well-being of new parents.
How similar studies have performed: While there have been studies on postpartum mental health, this specific approach to individualized screening using a web-based platform is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ≥ 19 years * 4-8 weeks postpartum * Proficiency to participate in English * Delivered within the province of British Columbia, Canada Exclusion Criteria: None.
Where this trial is running
Vancouver, British Columbia
- BC Women's Hospital & Health Centre — Vancouver, British Columbia, Canada (RECRUITING)
Study contacts
- Study coordinator: Marianne Vidler, PhD, MSc
- Email: marianne.vidler@cw.bc.ca
- Phone: 604-875-2424
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 Anxiety, Postpartum Depression, Postpartum Disorder, Postoperative Pain, Sleep Wake Disorders, Quality of Life, Anger