RECRUITING

Maintenance TMS in Treatment Resistant Depression

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Electroconvulsive therapy (ECT) is one of the most efficacious treatments available for treatment-resistant depression (TRD). Although a maintenance ECT protocol exists, multiple barriers limit its use for long-term use. These barriers include procedure tolerability, cognitive side effects, financial burden, and unreliable social support to accompany patients for these treatments. On the other hand, a different modality of noninvasive neuromodulation called transcranial magnetic stimulation (TMS) can be performed in the outpatient setting and does not need anesthesia. The likelihood of cognitive adverse effects with TMS is much lower than with ECT. Our clinical question encompasses piloting a maintenance TMS regimen to maintain remission in treatment-resistant major depressive disorder. This will be a patient-preference clinical trial, with patients offered the choice to initiate maintenance TMS versus maintenance ECT after their index ECT sessions for treatment-resistant depression. There will be no randomization or placebo involved in this study.

Official Title

Transitioning From Maintenance ECT to Maintenance TMS in Treatment Resistant Depression

Quick Facts

Study Start:2025-04-17
Study Completion:2026-04-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06682299

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients treated for TRD who have achieved remission through an index series of ECT
  2. * Able to provide informed consent
  3. * Age between 18 and 65 years
  4. * Deemed appropriate for maintenance TMS by their psychiatrist
  5. * Right-handed
  1. * History of seizures or a seizure disorder
  2. * Related neurological disorder, or any other medical condition that would preclude TMS treatment determined by the treatment team.

Contacts and Locations

Study Contact

Austin R Messner, MD
CONTACT
859-323-6861
austin.messner@uky.edu

Principal Investigator

Gopalkumar Rakesh, MD
STUDY_DIRECTOR
University of Kentucky

Study Locations (Sites)

University of Kentucky
Lexington, Kentucky, 40509
United States

Collaborators and Investigators

Sponsor: Austin Messner

  • Gopalkumar Rakesh, MD, STUDY_DIRECTOR, University of Kentucky

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-04-17
Study Completion Date2026-04-01

Study Record Updates

Study Start Date2025-04-17
Study Completion Date2026-04-01

Terms related to this study

Keywords Provided by Researchers

  • depression
  • tms
  • ect
  • treatment resistant depression
  • trd

Additional Relevant MeSH Terms

  • Treatment Resistant Depression (TRD)