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CompletedNCT03260257Updated Jun 4, 2024

A Neurofeedback Intervention to Improve Working Memory in Schizophrenia

An interventional study of Neurofeedback in Schizophrenia, sponsored by University of California, San Diego. Completed at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2024-06-04.

Sponsored by University of California, San Diego · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
64
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Schizophrenia affects 2.4 million Americans and causes significant individual and societal costs. Cognitive deficits including poor working memory arise early in the course of illness, account for poor long-term outcomes and have been difficult to treat with available treatments. The investigators are proposing to develop a novel, computer-based brain training to improve working memory in schizophrenia patients, which, if successful could have significant personal, societal, and economic impact.

Read the detailed description

Schizophrenia (SCZ) is a chronic debilitating mental disorder that affects 2.4 million Americans and leads to considerable individual and societal costs. In patients with SCZ, cognitive deficits (CD) occur early in the course of the illness, are associated with more severe illness, and are the best predictor of functional outcomes. Nonetheless, to date, CD have been difficult to treat using available treatments. Recent studies suggest CD in patients with SCZ may arise from abnormal synchronization of distributed neural networks. Synchronization or synchronous firing of neurons, binds cortical areas into functional networks in a task and state-dependent manner. Thus novel therapies that improve abnormal neural synchrony may improve previously refractory symptoms arising from disordered brain networks.

Neural synchrony or coherence in the gamma band (GBR, 30-45Hz) plays a central role in top-down attention, multisensory processing, perceptual binding and working memory (WM). Patients with SCZ exhibit abnormal GBR, and the magnitude of impairment is associated with the severity of cognitive disorganization. Given these results, improving GBR should improve CD, including WM in SCZ. This hypothesis has been tested and confirmed using repetitive transcranial magnetic stimulation (rTMS). Additionally, EEG-based neurofeedback (NFB) is hypothesized to improve GBR and cognitive function in patients with SCZ. NFB is a low-cost, easily administered and well-tolerated treatment. In healthy controls, Gamma-NFB improves GBR and cognitive function including WM. Thus, the investigators propose testing the feasibility and effectiveness of improving GBR using gamma-NFB in patients with SCZ using the framework of the R61/R33 mechanism.

The first trial (R61) is a proof-of-concept study designed to assess target engagement and dose response curve. Thirty SCZ patients will receive G-NFB training for 12 weeks (2 weekly sessions of 30minute duration) and be assessed for 1) evidence of training, 2) Change in GBR, 3) Change in WM and 4) Change in community functioning. The second trial (R33) aims to confirm target engagement based on training parameters obtained from R61, and to assess whether G-NFB is superior to an active-placebo neurofeedback intervention in improving GBR, WM and community functioning.

02

Conditions studied

  • Schizophrenia

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Keywords

  • Neurofeedback, Gamma band response
03

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Diagnosis of schizophrenia/schizoaffective disorder

Exclusion criteria

Exclusion Criteria:

  • Active substance use disorders in the last 30 days
  • Medication changes in the last 30 days
  • History of traumatic brain injury
  • seizure disorder
  • pregnancy
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
64 participants (actual)

Study arms

  • Experimental
    Schizophrenia patients

    Thirty SCZ patients will receive neurofeedback to enhance gamma band response in an open-label, proof of concept study.

    Other: Neurofeedback

Interventions

  • OtherNeurofeedback

    Neurofeedback (NFB) will be administered to improve gamma band response. NFBs effects will be measured on gamma coherence and working memory.

05

What researchers measure

Primary outcomes

  1. Change in Task related Gamma band response (gamma coherence and power)

    Gamma-NFBs effects on gamma coherence and gamma power over time will be assessed.

    Time frame: This variable will be assessed at t=0, 4 weeks, 8 weeks, 12 weeks and 4 weeks post completion of intervention

Secondary outcomes

  1. Change in Working memory

    Gamma-NFBs effects on non-verbal working memory will be assessed over time.

    Time frame: This variable will be assessed at t=0, 12 weeks, and 4 weeks post study completion.

06

Study locations

1 site
  • University of California at San Diego
    La Jolla, California 92093, United States
07

References and documents

Publications

  • Lin Y, Shu IW, Hsu SH, Pineda JA, Granholm EL, Singh F. Novel EEG-Based Neurofeedback System Targeting Frontal Gamma Activity of Schizophrenia Patients to Improve Working Memory. Annu Int Conf IEEE Eng Med Biol Soc. 2022 Jul;2022:4031-4035. doi: 10.1109/EMBC48229.2022.9870878. PubMed 36085679 ↗

Study documents

  • Informed consent form · Aug 16, 2022

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

08

Registry details

Key details

Study ID
NCT03260257
Lead sponsor
University of California, San Diego
Collaborators
National Institutes of Health (NIH)
Responsible party
Fiza Singh (Assistant Clinical Professor, University of California, San Diego) — Principal investigator
First posted
Aug 24, 2017
Start date
Mar 1, 2018
Primary completion
Apr 1, 2024
Completion
Apr 1, 2024
Last update
Jun 4, 2024

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2024. You cannot join it, but the record below documents what was studied.

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