NCT06242717

Postpartum Screening for Anxiety and Comorbid Conditions

Postpartum Screening for Anxiety and Comorbid Conditions: A Prospective British Columbia Cohort Study

• Status: Unknown
• Phase: —
• Study type: Observational
• Enrollment: 550 (estimated)
• Sponsor: University of British Columbia · Academic / Other
• Sex: Female
• Age: 19 Years
• Healthy volunteers: Accepted

Summary

The goal of this project is to facilitate the design of individualized postpartum anxiety (PPA) screening strategies in British Columbia (BC), Canada. A cohort of postpartum people (n=550) will be invited to complete the following seven questionnaires at 4-8 weeks after delivery: 1. State-Trait Anxiety Inventory 2. Edinburgh Postnatal Depression Scale 3. Multidimensional Scale of Perceived Social Support 4. PROMIS (Patient-Reported Outcomes Measurement Information System) Emotional Distress-Anger, Short Form 5-a 5. Short Form Brief Pain Inventory 6. WHOQOL-BREF for assessing quality of life 7. PROMIS Sleep Disturbance Short Form 8-b and PROMIS Sleep-Related Impairment Short Form 8-a The investigators will evaluate the feasibility of screening for postpartum anxiety and comorbid conditions through a web-based platform in a diverse BC population. They will assess the usability of the platform and questionnaires through 12-15 follow-up interviews with study participants and responses to the System Usability Scale. Their analysis will also identify patient characteristics and comorbidities (e.g., anger, pain, sleep disturbance) associated with a positive screen for postpartum anxiety.

Conditions

• Postpartum Anxiety
• Postpartum Depression
• Postpartum Disorder
• Postoperative Pain
• Sleep Wake Disorders
• Quality of Life
• Anger

Timeline

• Start date: 2023-11-09
• Primary completion: 2024-12-31
• Completion: 2024-12-31
• First posted: 2024-02-05
• Last updated: 2024-02-23

Locations

1 site across 1 country: Canada