D-Cycloserine + TMS for Mental Health
(NOCICEPT Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This study is testing whether combining a rapid form of transcranial magnetic stimulation (TMS), an oral medication called d-cycloserine (DCS), and therapy can improve brain flexibility and emotional control in adults experiencing moderate-to-severe depression, anxiety, or trauma symptoms. TMS is a non-invasive treatment that uses gentle magnetic pulses to stimulate specific areas of the brain.
In this phase of the study, all participants receive active accelerated TMS (delivering multiple brief sessions in a single day) along with DCS, a medication that helps enhance brain learning and plasticity. Participants will be randomly assigned to have TMS directed at one of two brain targets: a region called the precuneus (identified using personalized brain scans) or the dorsolateral prefrontal cortex (a standard area for mood treatment). Afterward, participants are randomly assigned to complete three weeks of either therapist-led talk therapy (a modified Unified Protocol) or self-guided educational videos and readings. The main goals are to determine which brain stimulation target works best and to see whether therapist-led therapy leads to more lasting symptom relief and brain changes compared to self-guided education.
Are You a Good Fit for This Trial?
This trial is for adults with moderate-to-severe depression, anxiety, or trauma symptoms. Participants should not have conditions that would make TMS unsafe (like certain metal implants) and must be able to take oral medication and participate in therapy or educational sessions.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- D-Cycloserine (DCS)
- Transcranial Magnetic Stimulation (TMS)
Trial Overview
The study tests if combining rapid transcranial magnetic stimulation (TMS), the medication d-cycloserine (DCS), and either therapist-led talk therapy or self-guided education can improve emotional control in people with mental health issues. Brain targets for TMS are assigned randomly.
How Is the Trial Designed?
4
Treatment groups
Experimental Treatment
TMS targeted to the precuneus followed by Unified Protocol (therapy) administered by a therapist
TMS targeted to the precuneus followed by self-led psychoeducation
TMS targeted to the DLPFC followed by Unified Protocol (therapy) administered by a therapist
TMS targeted to the DLPFC followed by self-led psychoeducation
Find a Clinic Near You
Who Is Running the Clinical Trial?
Mclean Hospital
Lead Sponsor
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