Accelerated iTBS for Post Partum Depression

Status Recruiting

Clinical Trial Summary

The investigators are studying the feasibility and tolerability of 10x/day intermittent theta burst (excitatory) transcranial magnetic stimulation to the left dorsolateral prefrontal cortex over the course of 6 days for women with post-partum depression. The investigators further hope to characterize the anticipated anti-depressant effect of this treatment paradigm.

Clinical Trial Description

This is an open-label study designed to investigate the feasibility and tolerability of a novel TMS treatment protocol to treat depression in women with post-partum depression. It is known that TMS can effectively treat depression. The FDA approved protocol lasts 6 weeks and is not feasible for many women with post-partum depression. The investigators are investigating a 6 day treatment for depression which may be more acceptable for this population. The investigators further hope to characterize the ant-depressant effect of this protocol in order to design a larger trial. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03417960
Study type	Interventional
Source	Medical University of South Carolina
Contact	Lisa McTeague, PhD
Phone	843-792-8274
Email	mcteague@musc.edu
Status	Recruiting
Phase	N/A
Start date	January 24, 2018
Completion date	July 31, 2024

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT03665038` - A Study to Assess the Safety of Brexanolone in the Treatment of Adolescent Female Participants With Postpartum Depression (PPD)	Phase 3
Recruiting	`NCT06042972` - Risk of Maternal Depression From 1 Year to 4 Years Postpartum in Yvelines
Completed	`NCT04813341` - Effectiveness of Mat Pilates and Aerobic Training on Fatigue and Depression	N/A
Terminated	`NCT04998565` - Add-on Effectiveness of EA or TENS in Early Postpartum Breast Engorgement	N/A
Completed	`NCT04135612` - The Impact of a Daily Smartphone-based Communication Among Postpartum Women on Breastfeeding Rates	N/A
Recruiting	`NCT05595486` - Baby2Home (B2H) Mobile Health Application	N/A
Not yet recruiting	`NCT04516668` - Effect of Tele-consultation in Addition With Psychiatric Follow-up During COVID-19 in Women Who Have Medical History of Post-partum Depression
Completed	`NCT05215028` - Optimization of Mother-child Dyad Follow-up by a Multidomain Application: Real-world Cross Sectional Study
Recruiting	`NCT04129476` - Effect of a Cooperative Education Program Based on Precede-Proceed Model During Pregnancy on Postpartum Depression	N/A
Recruiting	`NCT04193462` - Relationship-Based Intervention for Post-Partum Depression	N/A
Completed	`NCT03638687` - Neuroimaging Epigenetics of Prospective Postpartum Depression Biomarkers
Active, not recruiting	`NCT03052374` - Video-Feedback Interaction Guidance for Improving Interactions Between Depressed Mothers and Their Infants ("VID-KIDS")	N/A
Active, not recruiting	`NCT04940585` - ROSE in Sunset Park	N/A
Terminated	`NCT04011592` - Efficacy And Tolerability Of Sub-Anesthetic Ketamine In Postpartum Depression	Phase 2
Recruiting	`NCT05887115` - Nurse Family Partnership for Women With Previous Live Births	N/A
Completed	`NCT04818047` - Adaptation and Pilot Testing of Web and Mobile Interface for the VID-KIDS Intervention	N/A
Not yet recruiting	`NCT05643898` - "Mamá, te Entiendo" App-based Intervention for Reducing Depressive Symptoms in Postpartum Women	N/A
Terminated	`NCT04264520` - Initial Intervention Efficacy for an Online PTSD Intervention for Pregnant Women	N/A
Recruiting	`NCT04845347` - A Wearable Morning Light Treatment for Postpartum Depression	N/A
Enrolling by invitation	`NCT05186272` - mHealth Mindfulness Intervention for Pregnant Black and Latina Women at Risk of Postpartum Depression	Phase 3