Anxiety Disorders Clinical Trial
— PATHOfficial title:
Examining the Impact of Trauma-informed Cognitive Behavioural Therapy Among At-risk Pregnant Women on Perinatal Mental Health Outcomes: A Pilot Study
Verified date | May 2019 |
Source | Western University, Canada |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Intimate partner violence (IPV) is a significant and pervasive public health challenge and is associated with mental illnesses such as depression, anxiety and posttraumatic stress disorder (PTSD). Although the perinatal period may be a time of greater risk for experiencing IPV, and greater vulnerability to PTSD symptomatology, a lack of research exists pertaining to the identification/treatment of IPV-related PTSD symptoms during this period. Utilizing a mixed-methods approach, and employing a feminist, intersectional framework, the effectiveness of trauma-informed cognitive behavioural therapy (CBT) among pregnant survivors of IPV experiencing PTSD symptomatology on depression, anxiety, PTSD and maternal-infant attachment will be explored.
Status | Completed |
Enrollment | 3 |
Est. completion date | December 1, 2018 |
Est. primary completion date | December 1, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: Women who received antenatal CBT treatment from the Perinatal Nurse Specialist at the Perinatal Mental Health Clinic (London Health Sciences Centre, London, ON, Canada) who are: - English speaking - Have symptoms consistent with PTSD, depression, and/or anxiety Exclusion Criteria: - Women will be excluded if there is, or if it anticipated that there will be involvement in child protection services under the Child and Family Services Act |
Country | Name | City | State |
---|---|---|---|
Canada | London Health Sciences | London | Ontario |
Lead Sponsor | Collaborator |
---|---|
Western University, Canada | London Health Sciences Centre |
Canada,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Maternal quality of life | Maternal quality of life will be measured using the World Health Organization Quality of Life - Brief questionnaire (WHOQOL-BREF). Higher scores denote higher quality of life. We are not using a cutoff score for this measure, as it is an exploratory question and we are only looking at trends in the data, and not statistically different results among groups. | Up to 52 weeks postpartum | |
Other | Maternal coping | Maternal coping will be measured using the proactive coping inventory | Up to 52 weeks postpartum | |
Primary | PTSD | PTSD severity will be measured using the PTSD Checklist - Civilian Version | Up to 52 weeks postpartum | |
Secondary | Maternal-infant attachment | Maternal-infant attachment will be measured using the Maternal Attachment Inventory | Up to 52 weeks postpartum | |
Secondary | Presence of postpartum depression | Presence of depressive symptoms will be measured using the Edinburgh Postnatal Depression Scale (EPDS). Scores greater than 12 on the EPDS will be considered positive for postpartum depression. Scores between 0-12 will be considered "low probability of depression", scores 13 and above (13-30) will be considered "high probability of depression" | Up to 52 weeks postpartum | |
Secondary | Anxiety | Severity of anxiety will be measured using the State-Trait Anxiety Inventory | Up to 52 weeks postpartum |
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