← Back to Search

Behavioral Intervention

CBT Workshop for Postpartum Depression

N/A
Waitlist Available
Led By Ryan Vann Lieshout, MD, PhD
Research Sponsored by McMaster University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks and 6 months
Awards & highlights

Summary

This trial will assess if a 1-day CBT-based workshop delivered by PHNs can be an effective and cost-effective way to treat postpartum depression and reduce its impact on the family.

Who is the study for?
This trial is for individuals who are at least 18 years old, have a baby under one year of age, and can communicate fluently in English. It's specifically designed to help those suffering from postpartum depression (PPD). People with bipolar disorder, psychotic disorders, or substance use disorders cannot participate.
What is being tested?
The study tests if a single-day Cognitive Behavioural Therapy (CBT) workshop led by Public Health Nurses can improve PPD symptoms more effectively than usual care alone. Participants will be randomly placed into two groups: one attending the CBT workshop and the other receiving standard postnatal care.
What are the potential side effects?
Since this intervention involves therapy rather than medication, there may not be direct side effects like with drugs. However, participants might experience emotional discomfort discussing personal issues during therapy.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks and 6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 weeks and 6 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Secondary study objectives
EQ-5D-5L
Edinburgh Postnatal Depression Scale (EPDS)
Generalized Anxiety Disorder 7-Item Scale
+7 more
Other study objectives
CBT Skills Questionnaire (CBTSQ)
Client Satisfaction Questionnaire (CSQ-8)
Fidelity of Intervention Delivery
+2 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Online 1-Day CBT-Based WorkshopExperimental Treatment1 Intervention
Participants assigned to the treatment arm will attend a day long CBT-based workshop delivered online by two trained public health nurses in addition to receiving usual care.
Group II: Treatment as UsualActive Control1 Intervention
Participants assigned to the control arm will continue to receive standard postnatal care from their healthcare providers.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
1-Day Cognitive Behavioural Therapy-Based Workshop
2022
N/A
~120

Find a Location

Who is running the clinical trial?

McMaster UniversityLead Sponsor
906 Previous Clinical Trials
2,612,790 Total Patients Enrolled
12 Trials studying Postpartum Depression
2,736 Patients Enrolled for Postpartum Depression
Ryan Vann Lieshout, MD, PhDPrincipal InvestigatorMcMaster University

Media Library

1-Day Cognitive Behavioural Therapy-Based Workshop (Behavioral Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05622305 — N/A
Postpartum Depression Research Study Groups: Online 1-Day CBT-Based Workshop, Treatment as Usual
Postpartum Depression Clinical Trial 2023: 1-Day Cognitive Behavioural Therapy-Based Workshop Highlights & Side Effects. Trial Name: NCT05622305 — N/A
1-Day Cognitive Behavioural Therapy-Based Workshop (Behavioral Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05622305 — N/A
~52 spots leftby Dec 2024
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Back to top