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Enhancing Prefrontal Oscillations and Working Memory in Early-course Schizophrenia (REDOCS)

F

Fabio Ferrarelli

Status

Enrolling

Conditions

Schizophrenia

Treatments

Device: sham intermittent Theta Burst Stimulation (iTBS)
Device: active intermittent Theta Burst Stimulation (iTBS)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05102929
1R01MH125816-01A1 (U.S. NIH Grant/Contract)
STUDY20050194

Details and patient eligibility

About

This study will investigate the effects of intermittent Theta Burst Stimulation (iTBS) on natural oscillatory frequency of the dorsolateral prefrontal cortex (DLPFC) and working memory in early-course schizophrenia (EC-SCZ). Transcranial magnetic stimulation (TMS) will be used to evoke oscillatory activity, and EEG will record the responses of EC-SCZ participants. A working memory task will also be incorporated in order to determine how DLPFC natural frequency (NF) is related to working memory performance. iTBS (active or sham) will be administered, then the oscillatory activity of DLPFC and working memory performance will be reassessed. The overarching goal is to determine whether iTBS can acutely enhance the oscillatory activity of the DLPFC and to evaluate the relationship between changes in the DLPFC and working memory performance.

Full description

The overarching goal of this proposal is to establish whether, by acutely enhancing dorsolateral prefrontal cortex (DLPFC) oscillatory deficits experimentally, there is a corresponding improvement in working memory (WM) function in early-course schizophrenia (EC-SCZ) patients. To achieve this goal, the investigators will perform TMS/EEG assessments of DLPFC and related oscillatory parameters and evaluate WM ability with the AX-Continuous Performance Task (AX-CPT) before and after two theta burst stimulation (TBS) sessions (intermittent (iTBS) and sham TBS of DLPFC) in 75 EC-SCZ patients.

Aim 1. Establish the acute effects of active vs. sham TBS on DLPFC oscillatory activity/NF of EC-SCZ patients. The investigators will iTBS to enhance DLPFC oscillatory activity/NF, as assessed with TMS/EEG, in EC-SCZ patients.

H1: TBS condition (active vs sham) will moderate the change in DLPFC oscillatory activity/NF from pre to post-TBS, such that DLPFC oscillatory activity/NF will increase following iTBS (but not sham).

Aim 2. Assess the impact of acute active vs. sham TBS on WM performance in EC-SCZ patients. The investigators will assess the acute impact of active vs. sham iTBS on WM performance in EC-SCZ patients.

H2: iTBS condition (active vs sham) will moderate the change in WM from pre- to post-TBS, such that AX-CPT performance will improve following iTBS (but not sham).

Aim 3. Examine the relationship between TBS-related changes in DLPFC oscillatory activity/NF and WM performance in EC-SCZ patients.

H3: iTBS-induced increase in DLPFC oscillatory activity/NF will predict better post-iTBS WM performance in EC-SCZ patients.

Enrollment

75 estimated patients

Sex

All

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. ages 18-40 years
  2. DSM diagnoses of Schizophrenia Spectrum Axis I disorders
  3. a duration of less than three years from beginning of psychosis, defined by report of symptoms and/or history of treatment, based on clinical guidelines employed in our UPMC psychoses clinics in Pittsburgh.

Exclusion criteria

  1. DSM intellectual developmental disorder
  2. significant head injury
  3. medical illness affecting brain structure or function
  4. significant neurologic disorder (e.g. seizure disorder)
  5. personal history or family history of epilepsy
  6. inability to provide informed consent
  7. concussion with loss of consciousness (LOC) greater than 10 minutes
  8. history of electroconvulsive therapy
  9. diabetes with associated seizures, loss of sensation/weakness in arms or legs, or momentary LOC
  10. pregnancy or postpartum (<6 weeks after delivery or miscarriage), as determined by self-report
  11. a psychotic illness with a temporal relation to substance use or head injury.
  12. current or past co-morbidity for alcohol or psychoactive substance dependence
  13. substance abuse, other than cannabis and/or alcohol, within the past one year

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

75 participants in 2 patient groups

active, then sham Intermittent Theta Burst Stimulation (iTBS) over DLPFC
Experimental group
Description:
This arm will first receive active iTBS stimulation and then sham iTBS over the left dorsolateral prefrontal cortex (DLPFC).
Treatment:
Device: active intermittent Theta Burst Stimulation (iTBS)
Device: sham intermittent Theta Burst Stimulation (iTBS)
sham, then active intermittent Theta Burst Stimulation (iTBS) over DLPFC
Experimental group
Description:
This arm will first receive sham iTBS (i.e., with the TMS coil in the placebo orientation) and then active iTBS stimulation over the left dorsolateral prefrontal cortex (DLPFC).
Treatment:
Device: active intermittent Theta Burst Stimulation (iTBS)
Device: sham intermittent Theta Burst Stimulation (iTBS)

Trial contacts and locations

1

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Central trial contact

Sabine Janssen

Data sourced from clinicaltrials.gov

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