Testing a 4-Week Mindfulness Program for Anxiety Disorders in Mothers During the First Year After Giving Birth
Led by St. Joseph's Healthcare Hamilton · Updated on 2025-12-04
50
Participants Needed
2
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Postpartum anxiety PPA affects up to 20% of mothers in the first year after delivery, causing both psychological and physical symptoms. Current treatments improve some psychological aspects like anxiety and mood but often do not help with emotion regulation ER or bodily awareness, which are important for those with PPA. This research aims to test a mindfulness intervention designed to improve anxiety symptoms, ER, and bodily awareness in postpartum mothers with anxiety disorders, using both self-reports and brain imaging for a thorough evaluation.
Participants will be randomly assigned to receive either a 4-week mindfulness-based intervention or be placed on a waitlist receiving usual care. The mindfulness program is tailored specifically for postpartum mothers with clinical anxiety, adapted from established cognitive therapy methods to address anxiety during the postpartum period. The intervention focuses on both psychological and physical symptoms, with brain imaging done before and immediately after the intervention.
Participants will complete self-report questionnaires at enrollment, immediately post-intervention, and again 4 weeks later to measure anxiety, emotion regulation, worry, depression, quality of life, stress, bodily awareness, mindfulness, bonding, social support, and relationship adjustment. Brain scans fMRI will be conducted at enrollment and right after the 4-week intervention. This comprehensive monitoring will help researchers understand how the mindfulness program affects anxiety and related symptoms over time.
CONDITIONS
Brief Title
Psychological and Physiological Impact of a Mindfulness-based Intervention on Anxiety Disorders During the Postpartum Period
Research Team
S
Sheryl M Green, Ph.D., C.Psych
Z
Zoryana Babiy, M.Sc.
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Mothers or birthing parents aged 18 years and older who are between 0 and 12 months postpartum
Principal diagnosis of an anxiety disorder with or without comorbid depression
Not currently receiving psychological treatment
Not taking psychoactive medication or on stable medication for at least 8 weeks prior to the study and stable throughout the study
Fluent in English with at least a grade 8 reading level
You will not qualify if you...
Severe depression or suicidality requiring acute intervention
Psychotic disorders or current alcohol or substance use disorders
Severe claustrophobia
Presence of metallic objects in the body such as implants or pacemakers
Currently pregnant
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Outpatient Treatment
Duration - 4 weeks
Participants undergo a 4-week mindfulness-based intervention designed specifically for postpartum mothers and birthing parents with clinical anxiety.
Weekly visits during the 4-week intervention
Follow-up
Duration - 3 months
Participants are followed for 3 months after completing the intervention to assess ongoing psychological and physiological outcomes.
1 follow-up visit at 3 months post-intervention
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Published Research Related To This Trial
Mindfulness-Based Intervention for Treatment of Anxiety Disorders During the Postpartum Period: A 4-Week Proof-of-Concept Randomized Controlled Trial Protocol.