Summary

Eligibility
for people ages 18-70 (full criteria)
Location
at La Jolla, California and other locations
Dates
study started
estimated completion

Description

Summary

In this proposal the investigators will use an accelerated TMS protocol that concentrates the magnetic stimulation that would usually occur over 6 weeks into 10 treatment sessions per days, for 5 consecutive days in patient with treatment-refractory depression. This protocol will build on a previously published study demonstrating clinical efficacy of intermittent theta-burst stimulation (iTBS) on left dorsolateral prefrontal cortex (L-dlPFC) in a treatment refractory population.

Official Title

A Within Study on the Effects of L-dlPFC Activation Through iTBS in Refractory Depression

Details

Major depressive disorder (MDD) is a disabling mental disorder with a lifetime prevalence of up to16% . Approximately 30% of MDD patients suffer treatment resistant depression (TRD), with at least 2 failed adequate trials of pharmacotherapy. Repetitive transcranial magnetic stimulation (rTMS) has been shown to be a safe treatment for TRD, yet the standard clinical technique for using it as treatment depressive disorders is associated with limited efficacy to date. Among the potential causes of limited efficacy have been the scalp based targeting technique that is currently the most common targeting method rather than techniques that incorporate functional magnetic resonance imaging (fMRI) neuronavigation, which have been shown to have greater efficacy. Image guided TMS can target specific functional brain networks with greater resolution that takes into account individual differences in brain anatomy. Another technique for improving treatment efficacy, shown to modulate cortical excitability, may be the application of intermittent theta-burst stimulation in regular intervals, which has been shown to be no different than a longer-in-time application of rTMS. Paired with the evidence that iTBS has produced significant antidepressant responses in severely depressed individuals, and that relapse in depressive states predicts diminished efficacy of treatment as well as increased quantity of TBS pulses to have a beneficial effect, these recent iTBS findings suggest that iTBS may offer a valid treatment alternative to options that have proven otherwise ineffective in treating TRD. Therefore, the investigators aim to administer iTBS to severely-depressed participant in a shorter amount of time, in order to improve their antidepressant outcome. Significance: This protocol builds on different notions: 1. iTBS is not different in treatment outcome than rTMS while applying the same amount of pulses in shorter amount of time; 2. The degree of treatment resistance is indicative of iTBS quantity needed to obtain an antidepressant treatment 3. Repeated iTBS produces a significant effect in treating refractory depression 4. Decreasing the interval between iTBS applications enhanced positive treatment outcomes. Therefore, the compression of iTBS pulses with shorter intervals between sessions is hypothesized to have an increased beneficial effect on individuals affected by treatment-resistant depression.

Keywords

Treatment Resistant Depression TMS fMRI Depression Depressive Disorder, Treatment-Resistant intermittent Theta Burst Stimulation Compressed iTBS schedule

Eligibility

You can join if…

Open to people ages 18-70

  • Gender, inclusive
  • 18 - 70 years of age
  • Meets Diagnostic and Statistical Manual of Mental Disorders criteria for primary diagnosis of MDD
  • Patients must be fluent in English
  • Participants must have the ability to provide consent
  • Montgomery Asberg Depression Rating Scale score ≥20
  • Failed 2+ prior treatments (treatment-refractory)
  • May be on current anti-depressant medication at the discretion of PI, if not exceeding doses that would make TMS an increased risk

You CAN'T join if...

  • Pregnancy (Female participants)
  • MRI contraindication
  • Medical condition that interferes with the collection or interpretation of MRI data
  • Implanted devices such as: aneurysm clip or cardiac pacemaker
  • Diagnosis of stroke, epilepsy, or other neurological disorders interfering with treatment at PI discretion
  • Any factor the investigator believe may affect participant safety or compliance (ex: ≥100 miles from clinic)
  • Current alcohol or substance use disorder in last 3 months

Locations

  • Department of Interventional Psychiatry, University of California San Diego
    La Jolla California 92093 United States
  • Center for Neuromodulation in Depression and Stress
    Philadelphia Pennsylvania 19104 United States

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of Pennsylvania
ID
NCT04684706
Study Type
Interventional
Participants
Expecting 30 study participants
Last Updated